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1.

図書

図書
R. Blumenhagen, E. Plauschinn
出版情報: Berlin : Springer, c2009  xi, 265 p. ; 25 cm
シリーズ名: Lecture notes in physics ; 779
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Introduction / 1:
Basics in Conformal Field Theory / 2:
he Conformal Group / 2.1:
Conformal Invariance / 2.1.1:
Conformal Group in d ? 3 / 2.1.2:
Conformal Group in d ? 2 / 2.1.3:
Primary Fields / 2.2:
The Energy-Momentum Tensor / 2.3:
Radial Quantisation / 2.4:
The Operator Product Expansion / 2.5:
Operator Algebra of Chiral Quasi-Primary Fields / 2.6:
Conformal Ward Identity / 2.6.1:
Two- and Three-Point Functions / 2.6.2:
General Form of the OPE for Chiral Quasi-Primary Fields / 2.6.3:
Normal Ordered Products / 2.7:
The CFT Hilbert Space / 2.8:
Simple Examples of CFTs / 2.9:
The Free Boson / 2.9.1:
The Free Fermion / 2.9.2:
The (b,c) Ghost Systems / 2.9.3:
Highest Weight Representations of the Virasoro Algebra / 2.10:
Correlation Functions and Fusion Rules / 2.11:
Non-Holomorphic OPE and Crossing Symmetry / 2.12:
Fusing and Braiding Matrices / 2.13:
Further Reading
Symmetries of Conformal Field Theories / 3:
Ka?-Moody Algebras / 3.1:
The Sugawara Construction / 3.2:
Highest Weight Representations of Sû(2)k / 3.3:
The Sô(N)1 Current Algebra / 3.4:
The Knizhnik-Zamolodchikov Equation / 3.5:
Coset Construction / 3.6:
W Algebras / 3.7:
Conformal Field Theory on the Torus / 4:
The Modular Group of the Torus and the Partition Function / 4.1:
Examples for Partition Functions / 4.2:
The Free Boson on a circle / 4.2.1:
The Free Boson on a circle of Radius R=?2k / 4.2.3:
The Free Boson Orbifold / 4.2.4:
The Verlinde Formula / 4.3:
The Sû(2)k Partition Functions / 4.4:
Modular Invariants of Virc<1 / 4.5:
The Parafermions / 4.6:
Simple Currents / 4.7:
Additional Topics / 4.8:
Asymptotic Growth of States in RCFTs / 4.8.1:
Dilogarithm Identities / 4.8.2:
Supersymmetric Conformal Field Theory / 5:
N=1 Superconformal Models / 5.1:
N=2 Superconformal Models / 5.2:
Chiral Ring / 5.3:
Spectral Flow / 5.4:
Coset Construction for the N ? 2 Unitary Series / 5.5:
Gepner Models / 5.6:
Massless Models of Gepner Models / 5.7:
Boundary Conformal Field Theory / 6:
The Boson with Boundaries / 6.1:
Boundary Conditions / 6.1.1:
Partition Function / 6.1.2:
Boundary States for the Free Boson / 6.2:
Tree-Level Amplitudes / 6.2.1:
Boundary States for RCFTs / 6.3:
CFTs on Non-Orientable Sufraces / 6.4:
Crosscap States for the Free Boson / 6.5:
Crosscap States for RCFTs / 6.6:
he Orientifold of the Bosonic String / 6.7:
Concluding Remarks
General Books on CFT and String Theory|259
Index
Introduction / 1:
Basics in Conformal Field Theory / 2:
he Conformal Group / 2.1:
2.

図書

図書
edited by Heinz Gerischer and Charles W. Tobias ; contributions from V. Brusic ... [et al.]
出版情報: Weinheim ; New York : VCH, c1990-  v. ; 25 cm
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Marcus Theory in the Qualitative and Quantitative Description of Electrochemiluminescence Phenomena / A. Kapturkiewicz
Electrochemistry of Oxide High-Temperature Superconductors / O. Petrii ; G. Tsirlina
Flow Rate Dependence of Localized Corrosion in Thermal Power Plant Materials / D. Macdonald ; L. Kriksunov
Polymer Electrolyte Fuel Cells / S. Gottesfeld
Graphite, Carbonaceous Materials and Organic Solids as Active Electrodes in Metal-Free Batteries / F. Beck
Index
Series Preface
Volume Preface
List of Contributors
In-situ X-ray Diffraction Studies of the Electrode/Solution Interface / Christopher A. Lucas ; Nenad M. Markovic1:
Introduction / 1.1:
Experimental / 1.2:
Adsorbate-induced Restructuring of Metal Substrates / 1.3:
Surface Relaxation / 1.3.1:
Pt Monometallic and Bimetallic Surfaces / 1.3.1.1:
Group IB Metals / 1.3.1.2:
Surface Reconstruction / 1.3.2:
Adlayer Structures / 1.4:
Anion Structures / 1.4.1:
CO Ordering on the Pt(111) Surface / 1.4.2:
Underpotential Deposition (UPD) / 1.4.3:
Reactive Metals and Oxides / 1.5:
Conclusions and Future Directions / 1.6:
Acknowledgments
References
UV-visible Reflectance Spectroscopy of Thin Organic Films at Electrode Surfaces / Takamasa Sagara2:
The Basis of UV-visible Reflection Measurement at an Electrode Surface / 2.1:
Absolute Reflection Spectrum versus Modulated Reflection Spectrum / 2.3:
Wavelength-modulated UV-visible Reflectance Spectroscopy / 2.4:
Potential-modulated UV-visible Reflectance Spectroscopy / 2.5:
Instrumentation of the Potential-modulated UV-visible Reflection Measurement / 2.6:
ER Measurements for Redox-active Thin Organic Films / 2.7:
Interpretation of the Reflection Spectrum / 2.8:
Reflection Measurement at Special Electrode Configurations / 2.9:
Estimation of the Molecular Orientation on the Electrode Surface / 2.10:
Estimation of the Molecular Orientation on the Electrode Surface using the Redox ER Signal / 2.10.1:
Estimation of the Molecular Orientation on the Electrode Surface using the Stark Effect ER Signal / 2.10.2:
Measurement of Electron Transfer Rate using ER Measurement / 2.11:
Redox ER Signal in Frequency Domain / 2.11.1:
Examples of Electron Transfer Rate Measurement using ER Signal / 2.11.2:
Improvement in Data Analysis / 2.11.3:
Combined Analysis of Impedance and Modulation Spectroscopic Signals / 2.11.4:
Upper Limit of Measurable Rate Constant / 2.11.5:
Rate Constant Measurement using an ER Voltammogram / 2.11.6:
ER Signal Originated from Non-Faradaic Processes - a Quick Overview / 2.12:
ER Signal with Harmonics Higher than the Fundamental Modulation Frequency / 2.13:
Distinguishing between Two Simultaneously Occurring Electrode Processes / 2.14:
Some Recent Examples of the Application of ER Measurement for a Functional Electrode / 2.15:
Scope for Future Development of UV-visible Reflection Measurements / 2.16:
New Techniques in UV-visible Reflection Measurements / 2.16.1:
Remarks on the Scope for Future Development of UV-visible Reflection Measurements / 2.16.2:
Epi-fluorescence Microscopy Studies of Potential Controlled Changes in Adsorbed Thin Organic Films at Electrode Surfaces / Dan Bizzotto ; Jeff L. Shepherd3:
Fluorescence Microscopy and Fluorescence Probes / 3.1:
Fluorescence near Metal Surfaces / 3.3:
Description of a Fluorescence Microscope for Electrochemical Studies / 3.4:
Microscope Resolution / 3.4.1:
Image Analysis / 3.4.2:
Electrochemical Systems Studied with Fluorescence Microscopy / 3.5:
Adsorption of C[subscript 18]OH on Au(111) / 3.5.1:
The Adsorption and Dimerization of 2-(2[prime]-Thienyl)pyridine (TP) on Au(111) / 3.5.2:
Fluorescence Microscopy of the Adsorption of DOPG onto an Hg Drop / 3.5.3:
Fluorescence Microscopy of Liposome Fusion onto a DOPC-coated Hg Interface / 3.5.4:
Fluorescence Imaging of the Reductive Desorption of an Alkylthiol SAM on Au / 3.5.5:
Conclusions and Future Considerations / 3.6:
Structures and Abbreviations
Linear and Non-linear Spectroscopy at the Electrified Liquid/Liquid Interface / David J. Fermin4:
Introductory Remarks and Scope of the Chapter / 4.1:
Linear Spectroscopy / 4.2:
Total Internal Reflection Absorption/Fluorescence Spectroscopy / 4.2.1:
Potential-modulated Reflectance/Fluorescence in TIR / 4.2.2:
Quasi-elastic Laser Scattering (QELS) / 4.2.3:
Other Linear Spectroscopic Studies at the Neat Liquid/Liquid Interface / 4.2.4:
Non-linear Spectroscopy / 4.3:
Second Harmonic Generation / 4.3.1:
Vibrational Sum Frequency Generation / 4.3.2:
Summary and Outlook / 4.4:
Symbols
Abbreviations
Sum Frequency Generation Studies of the Electrified Solid/Liquid Interface / Steven Baldelli ; Andrew A. Gewirth5:
Theoretical Background / 5.1:
SFG Intensities / 5.1.2:
Resonant Term / 5.1.3:
Non-resonant Term / 5.1.4:
Phase Interference / 5.1.5:
Orientation Information in SFG / 5.1.6:
Phase Matching / 5.1.7:
Surface Optics / 5.1.8:
Data Analysis Reference / 5.1.9:
Experimental Designs / 5.1.10:
Spectroscopy Cell / 5.1.11:
Applications of SFG to Electrochemistry / 5.2:
CO Adsorption / 5.2.1:
Polarization Studies / 5.2.1.1:
Potential Dependence / 5.2.1.2:
CO on Alloys / 5.2.1.3:
Solvent Effects / 5.2.1.4:
Adsorption of upd and opd H / 5.2.2:
CN on Pt and Au Electrodes / 5.2.3:
CN/Pt / 5.2.3.1:
CN/Au / 5.2.3.2:
OCN and SCN / 5.2.4:
Pyridine and Related Derivatives / 5.2.5:
Dynamics of CO and CN Vibrational Relaxation / 5.2.6:
Solvent Structure / 5.2.7:
Nonaqueous Solvents / 5.2.7.1:
Aqueous Solvents / 5.2.7.2:
Monolayers and Corrosion / 5.2.8:
Conclusion / 5.3:
IR Spectroscopy of the Semiconductor/Solution Interface / Jean-Noel Chazalviel ; Francois Ozanam6:
IR Spectroscopy at an Interface / 6.1:
Basic Principles of IR Spectroscopy / 6.2.1:
External versus Internal Reflection / 6.2.2:
Practical Aspects at an Electrochemical Interface / 6.3:
How Potential can Affect IR Absorption / 6.3.1:
How to Isolate Potential-sensitive IR Absorption / 6.3.2:
What can be Learnt from IR Spectroscopy at the Interface / 6.4:
Vibrational Absorption of Interfacial and Double-Layer Species / 6.4.1:
Vibrational Absorption of Species outside the Double-Layer / 6.4.2:
Electronic Absorption / 6.4.3:
Effect of Light Polarization in ATR Geometry / 6.5:
Selection Rules for a Polarized IR Beam / 6.5.1:
Case of Strongly Polar Species: LO-TO Splitting / 6.5.2:
Polarization Modulation / 6.5.3:
Dynamic Information from a Modulation Technique / 6.6:
Case of Rough or Complex Interfaces / 6.7:
Surface Roughness / 6.7.1:
Composite Interface Films / 6.7.2:
Recent Advances in in-situ Infrared Spectroscopy and Applications in Single-crystal Electrochemistry and Electrocatalysis / Carol Korzeniewski6.8:
Spectrometer Systems / 7.1:
Spectrometer Throughput Considerations / 7.2.2:
Detectors / 7.2.3:
Signal-to-Noise Ratio Considerations / 7.2.4:
Signal Digitization / 7.2.5:
Signal Modulation and Related Data Acquisition Methods / 7.2.6:
Applications / 7.3:
Adsorption and Reactivity at Well-defined Electrode Surfaces / 7.3.1:
Adsorption on Pure Metals / 7.3.1.1:
Electrochemistry at Well-defined Bimetallic Electrodes / 7.3.1.2:
SEIRAS / 7.3.2:
Infrared Spectroscopy as a Probe of Surface Electrochemistry at Metal Catalyst Particles / 7.3.3:
A Nanostructured Electrodes and Optical Considerations / 7.3.4:
Emerging Instrumental Methods and Quantitative Approaches / 7.3.5:
Step-scan Interferometry / 7.3.5.1:
Two-dimensional Infrared Correlation Analysis / 7.3.5.2:
Quantitation of Molecular Orientation / 7.3.5.3:
Summary / 7.4:
In-situ Surface-enhanced Infrared Spectroscopy of the Electrode/Solution Interface / Masatoshi Osawa8:
Electromagnetic Mechanism of SEIRA / 8.1:
Experimental Procedures / 8.3:
Electrochemical Cell and Optics / 8.3.1:
Preparation of Thin-film Electrodes / 8.3.2:
General Features of SEIRAS / 8.4:
Comparison of SEIRAS with IRAS / 8.4.1:
Surface Selection Rule and Molecular Orientation / 8.4.2:
Comparison of SEIRA and SERS / 8.4.3:
Baseline Shift by Adsorption of Molecules and Ions / 8.4.4:
Selected Examples / 8.5:
Reactions of a Triruthenium Complex Self-assembled on Au / 8.5.1:
Cytochrome c Electrochemistry on Self-assembled Monolayers / 8.5.2:
Molecular Recognition at the Electrochemical Interface / 8.5.3:
Hydrogen Adsorption and Evolution on Pt / 8.5.4:
Oxidation of C1 Molecules on Pt / 8.5.5:
Advanced Techniques for Studying Electrode Dynamics / 8.6:
Rapid-scan Millisecond Time-resolved FT-IR Measurements / 8.6.1:
Step-scan Microsecond Time-resolved FT-IR Measurements / 8.6.2:
Potential-modulated FT-IR Spectroscopy / 8.6.3:
Summary and Future Prospects / 8.7:
Acknowledgements
Quantitative SNIFTIRS and PM IRRAS of Organic Molecules at Electrode Surfaces / Vlad Zamlynny ; Jacek Lipkowski9:
Reflection of Light from Stratified Media / 9.1:
Reflection and Refraction of Electromagnetic Radiation at a Two-phase Boundary / 9.2.1:
Reflection and Refraction of Electromagnetic Radiation at a Multiple-phase Boundary / 9.2.2:
Optimization of Experimental Conditions / 9.3:
Optimization of the Angle of Incidence and the Thin-cavity Thickness / 9.3.1:
The Effect of Incident Beam Collimation / 9.3.2:
The Choice of the Optical Window Geometry and Material / 9.3.3:
Determination of the Angle of Incidence and the Thin-cavity Thickness / 9.4:
Determination of the Isotropic Optical Constants in Aqueous Solutions / 9.5:
Determination of the Orientation of Organic Molecules at the Electrode Surface / 9.6:
Development of Quantitative SNIFTIRS / 9.7:
Description of the Experimental Set-up / 9.7.1:
Fundamentals of SNIFTIRS / 9.7.2:
Calculation of the Tilt Angle from SNIFTIRS Spectra / 9.7.3:
Applications of Quantitative SNIFTIRS / 9.7.4:
Development of Quantitative in-situ PM IRRAS / 9.8:
Fundamentals of PM IRRAS and Experimental Set-up / 9.8.1:
Principles of Operation of a Photoelastic Modulator / 9.8.3:
Correction of PM IRRAS Spectra for the PEM Response Functions / 9.8.4:
Background Subtraction / 9.8.5:
Applications of Quantitative PM IRRAS / 9.8.6:
Summary and Future Directions / 9.9:
Tip-enhanced Raman Spectroscopy - Recent Developments and Future Prospects / Bruno Pettinger10:
General Introduction / 10.1:
SERS at Well-defined Surfaces / 10.2:
Single-molecule Raman Spectroscopy / 10.3:
Tip-enhanced Raman Spectroscopy (TERS) / 10.4:
Near-field Raman Spectroscopy with or without Apertures / 10.4.1:
First TERS Experiments / 10.4.2:
TERS on Single-crystalline Surfaces / 10.4.3:
Outlook / 10.5:
Recent Results / 10.5.1:
New Approaches on the Horizon / 10.5.2:
Acknowledgment
Subject Index
Microelectrodes in Solid State Ionics (J
Fleig)
Nonlinear Dynamics in Electrochemical Systems (K
Krischer)
The Electrochemistry of Diamond (Y
Pleskov)
Passivity of Metals (H
Strehblow)
Marcus Theory in the Qualitative and Quantitative Description of Electrochemiluminescence Phenomena / A. Kapturkiewicz
Electrochemistry of Oxide High-Temperature Superconductors / O. Petrii ; G. Tsirlina
Flow Rate Dependence of Localized Corrosion in Thermal Power Plant Materials / D. Macdonald ; L. Kriksunov
3.

図書

図書
edited by Gerhart K. Gaulé
出版情報: New York : Plenum Press, c1965-  v. <2- > ; 24 cm
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4.

図書

図書
Rodd, E. H. ; Coffey, S. (Samuel) ; Ansell, Martin F. (Martin Frederick) ; Sainsbury, Malcolm
出版情報: Amsterdam ; Tokyo : Elsevier Pub. Co., 1973-  v. ; 23 cm
シリーズ名: Rodd's Chemistry of carbon compounds : a modern comprehensive treatise ; v. 4
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Contributor
Preface
List of common abbreviations and symbols used
Six-membered Ring Compounds with one Hetero-Atom: Oxygen / R. LivingstoneChapter 20:
Pyran and its derivatives / 1.:
Pyrans and pyrylium salts / (a):
2H- and 4H pyrans (2- and 4-pyrans, [alpha]-and [gamma]-pyrans) / (i):
Pyrylium salts / (ii):
2H-Pyran-2-ones ([alpha] or 2-pyrones) and 4H-pyran-4-ones ([gamma] or 4-pyrones) / (b):
2H-Pyrones
4H-Pyrones
Hydroxy-2H-pyran-2-ones (hydroxy-2H-pyrones, hydroxy-2-pyrones, hydroxy-[alpha]-pyrones) / (iii):
Hydroxy-4H-pyran-4-ones (hydroxy-4H-pyrones, hydroxy-4-pyrones, hydroxy-[gamma]-pyrones) / (iv):
Hydropyrans / 2.:
Dihydropyrans and derivatives
3,4-Dihydro-2H-pyrans (2,3-dihydro-4H-pyrans)
3,4-Dihydro-2H-pyran-2-, 3-, and 4-ones (3,4-dihydro-2, 3-, and 4-pyrones)
3,4-Dihydro-2H-pyran-2,4-diones
5,6-Dihydro-2H-pyrans, 3,6-dihydro-2H-pyrans
5,6-Dihydro-2H-pyran-2-, -5, and-6-ones (3,6-dihydro-2H-pyran-6-, -3- and -2-ones) / (v):
3,6-Dihydro-2H-pyran-2,6-diones, 5,6-dihydro-2H-pyran-2,6-diones / (vi):
Tetrahydropyrans and derivatives
Tetrahydropyran, alkyl and aryl substituted tetrahydropyrans and related derivatives
Tetrahydropyranols and derivatives
Hydroxyalkyltetrahydropyrans and related compounds
Tetrahydropyran-carboxaldehydes
Tetrahydro-pyrancarboxylic acids and esters
Halogenotetrahydropyrans
Cyano-, nitro-, and amino-tetrahydropyrans and related compounds / (vii):
Tetrahydropyran-2, -3-, and -4-ones / (viii):
Benzo[b]pyrans (1-benzopyrans, 5,6-benzopyrans, chromenes) and their derivatives / 3.:
Benzo[b]pyrans and their oxidation products
Alkyl- and alylbenzo[b]pyrans and flavenes
Naturally occurring derivatives of 2,2-dimethyl-2H-benzo[b]pyran
Benzopyrylium or chromylium and flavylium salts
Coumarin (2H-benzo[b]pyran-2-one, 5,6-benzo-2-pyrone, 5,6-benzo-[alpha]-pyrone) and its derivatives
Hydroxy-coumarins
Dihydroxycoumarins
Trihy-droxycoumarins
Miscellaneous coumarin derivatives
Furocoumarins / (ix):
Pyrancoumarins / (x):
Chromones (4H)-benzo[b]pyran-4-ones, 5,6-benzo-4-pyrones, 5,6-benzo-y-pyrones) / (xi):
Miscellaneous compounds related to chromone / (xii):
Furochromones / (xiii):
Pyranochromones / (xiv):
Flavones (2-phenylchromones, 2-phenyl-4H-benzo[b]pyran-4-ones) and related derivatives / (xv):
Flavonols (3-hydroxyflavones, 3-hydroxy-2-phenyl-4H-benzo[b]pyran-4-ones) / (xvi):
Isoflavones (3-phenyl-chromones, 3-phenyl-4H-benzo[b]-pyran-4-ones) / (xvii):
Furoisoflavones / (xviii):
Chroman, dihydrochromene, 3,4-dihydro-2H-benzo[b]pyran and derivatives / 4.:
Chromans
Tocopherols
Phenylchromans (flavans and isoflavans) phenyl-2H-3,4-dihydrobenzo[b]-pyrans / (c):
Flavan, 2-phenylchroman, 2-phenyl-2H-3,4-dihydrobenzo[b]pyran derivatives
Isoflavans, 3-phenylchromans, 3-phenyl-2H-3,4-dihydrobenzo[b]pyran derivatives
Chromanols, hydroxychromans / (d):
Flavanols, 3-hydroxy-2-phenylchromans, 3-hydroxy-2-phenyl-3,4-dihydro-2H-benzo[b]pyran, catechins and related condensed tannins / (e):
Flavanols
Catechins
Flavan-4-ols
Chromanones, dihydrobenzo[b]pyranones / (f):
Chroman-2-ones, dihydrocoumarin
Chroman-3-ones
Chroman-4-ones
Chromandiones
Flavanones, 2-phenylchroman-4-ones, 2-phenyl-3,4-dihydro-2H-benzo[b]-pyran-4-one / (g):
Hydroxyflavanones / (h):
Biflavanones
Isoflavanones, 3-phenylchroman-4-ones, 3-phenyl-3,4-dihydro-2H-benzo[b]pyran-4-ones / (j):
1H-Benzo[c]pyran, 1H-2-benzopyran, isobenzopyran, 3,4-benzopyran, isochromene, and its derivatives / 5.:
1H-Benzo[c]pyrans
Benzo[c]pyrylium salts
Isocoumarin, 1H-benzo[c]pyran-1-one
3H[Benzo[c]pyran-3-ones
Isochroman, 3,4-dihydro-1H-benzo[c]pyran, 3,4-dihydro-1H-2-benzopyran and derivatives / 6.:
Isochroman
Isochromanones, 3,4-dihydroisocoumarins, and isochromandiones
Isochroman-1-ones
Isochroman-3-one
Isochromandiones
Tetrahydro- and perhydroisochroman derivatives and related compounds
Xanthene, dibenzo[b,e]pyran, 2,3:5,6-dibenzopyran and derivatives / 7.:
Xanthene derivatives
Xanthylium salts and xanthene colouring matters
Xanthones
Halogenoxanthones
Nitro- and aminoxanthones
Hydroxyxanthones and related compounds
Acylxanthones, xanthonecarboxylic acids and derivatives
Tetra-, hexa-, octa-, deca-, and perhydroxanthones and related compounds
Furoxanthones
6H-Dibenzo[b,d]pyran, 3,4-benzochromone and its derivatives / 8.:
Naphthopyrans, benzochromenes and derivatives / 9.:
Naphtho[1,2-b]-, [2,1-b], and [2,3-b]pyrans
Naphthol[1,2-b]pyrans
Naphtho[2,1-b]pyrans
Naphtho[1,2-b]- and [2,1-b]pyrans
Naphtho[2,3-b]-pyrans
Naphtho[1,2-c]- and [2,3-c]pyrans, isonaphthopyrans
Naphtho[1,8-b,c]- and [1,8-c,d]pyrans
Benzo- and dibenzoxanthone derivatives and miscellaneous pyran ring systems / 10.:
Six-membered Ring Compounds with One Hetero-Atom: Sulphur, Selenium, Tellurium, Silicon, Germanium, and Tin / Chapter 21.:
Thiopyran derivatives
Thiopyrans, thiopyrylium salts and thiopyrones
Thipyrans
Thiopyrylium salts
Thiopyranones
Di- and tetra-hydro-thiopyrans and -thiopranones
Dihydrothiopyrans, dihydrothiins, dihydrothiapyrans and related 2-, 3-, and 4-ones
Tetrahydrothiopyrans, thianes, tetra-hydrothiapyrans and related 3-and 4-ones
Benzo[b]thiopyrans, 1-benzothiopyrans, benzo[b]thiins, thiochromenes, 5,6-benzothiapyrans and derivatives
Benzo[b]thiopyrans, benzo[b]thiopyranones and related naphtho derivatives
Benzo[b]thiopyrans, 1-benzothiopyrans, benzo[b]thiins, thiochromenes
Benzothiopyrylium salts, 1-benzothiopyranylium salts, thiochromylium salts
Benzothiopyranones
Thiochromans, thiochromanones and related compounds
Thiochromans, 3,4-dihydro-2H-benzo[b]thiopyrans
Thiochromanones, 3,4-dihydro-2H-benzo[b]thiopyranones
Thiochromanols, 3,4-dihydro-2H-benzo[b]thiopyranols
Hexahydrobenzo[b]thiopyrans, hexahydro-1-benzothiopyrans, hexahydrothiochromens and octahydrobenzo[b]thiopyrans, octahydro-1-benzothiopyrans, octahydrothiochromens, hexahy-drothiochromans
1H-Benzo[c]thiopyran, 1H-2-benzothiopyran, isothiochromene, 3,4-benzothio-pyran and its derivatives
1H-Benzo[c]thiopyran, isothiochromene and derivatives
3,4-Dihydro-1H-benzo[c]thiopyran, 3,4-dihydro-1H-2-benzothiopyran, isothiochroman and its derivatives
Dibenzothiopyran, thioxanthene and derivatives
Thioxanthenes, thioxanthylium salts, and thioxanthenium salts
Thioxanthones, thioxanthen-9-ones
Dibenzo[b,d]thiopyrans
Naphthothiopyrans and related compounds
Naphthothiopyrans
Perinaphthothiopyrans, thiaphenalenes
Benzothioxanthene derivatives
Selenopyrans and related compounds
Selenopyrans and derivatives
Selenopyrans containing fused rings
Benzoselenopyrans and derivatives
Selenoxanthene and derivatives
Telluropyrans and related compounds
Telluropyrylium salts and tellurane, tetrahydrotelluropyran derivatives
Telluropyrans containing fused rings
Benzotelluropyrans
Telluroxanthenes
Compounds containing an element from Group 4
Silicon compounds
Silabenzene, silacyclohexenes and their derivatives
Silacyclohexane and derivatives
Polycyclic silanes with six-membered rings
Germanium and tin compounds
Germanium compounds
Tin compounds
Guide to the index
Index
List of contributors
Five-membered Monoheterocyclic Compounds Alkaloids (continued): Pyrrolidine Alkaloids / D.J. RobinsChapter 7.:
Pyrrolidine bases
Pyrrolidones
N-Acylpyrrolidines
N-Acylpyrrolidones
Five-membered Monoheterocyclic Compounds (continued): Pyrrolizidine Alkaloids / Chapter 8.:
Introduction
Synthesis of necines
Unhydroxylated compounds
Monohydroxylated necines
Dihydroxylated necines
Trihydroxylated necines
Tetrahydroxylated necines
Synthesis of macrocyclic pyrrolizidine alkaloids
Structures of pyrrolizidine alkaloids
Unesterified necines
Monoesters
Acyclic diesters
Cyclic diesters
The Indole Alkaloids / G.W. GribbleChapter 9.:
Alkaloids lacking a tryptamine unit
Simple indoles
Carbazole derivatives
Alkaloids containing a tryptamine unit
Compounds without an isoprene moiety
Simple tryptamine and tryptophan derivatives
Eserine types
[beta]-Carboline and reduced [beta]-carbolines
Compounds containing an isoprene- (but not terpene-) derived moiety
The ergot alkaloids
Mould metabolites
Compounds containing a terpene-derived moiety
Alkaloids of the Corynanthe-Strychnos unit
Alkaloids with a seco-type unit
Alkaloids with the Aspidosperma unit
Alkaloids containing the Iboga unit
Novel types
Bisindole alkaloids
Compounds containing two identical "halves" linked symmetrically
Calycanthaceous alkaloids
Calabash-curare alkaloids
Diketopiperazine alkaloids
Bis-indole quinones
Indolo[2,3-alpha]carbazoles and related alkaloids
Marine bis-indoles
Other symmetrical bis-indoles
Compounds not composed of identical halves nor linked symmetrically
Sesquimeric compounds
The secamines and presecamines
Bis-indoles from Vinca rosea
Bis-carbazoles
Duo-carmycins and related alkaloids
Simple bis-indoles
Other complex bis-indole alkaloids
Five-membered Monoheterocyclic Compounds, Amaryllidaceae Alkaloids / J.R. LewisChapter 10.:
Biogrenesis
Biological activity
Table 1. New amaryllidaceae alkaloids (1987-1994) and their botanical sources
X-ray structure determination
Lycorine type alkaloids
Isolation and structural studies
Synthesis
Lycorenan type alkaloids (lycorenines and homolycorines)
Crinine type alkaloids
Galannthamine type alkaloids
Pancracine type alkaloids
Phenanthridine alkaloids / 11.:
Miscellaneous alkaloids / 12.:
Benzylidene-phenylethylamines and belladines
4-Phenyltetrahydroisoquinolines
Mesembrinanes
Tropane Alkaloids / G. FodorChapter 11:
Synthesis of tropanes
Stereochemistry of the ring nitrogen in tropanes
Established alkaloids
New tropane alkaloids
New cocaine alkaloids
Biosynthesis
Biological activity of some tropane alkaloids
Pyrrole Pigments / K.M. SmithChapter 12.:
Scope
Nomenclature
Porphyrins
Meso-tetra-arylporphyrins and other meso-arylporphyrins
Octa-substituted and related porphyrins
Petroporphyrins
Porphyrin oligomers
Chlorins and bacteriochlorins
Chlorophylls and derivatives
Other chlorins
Chlorins and bacteriochlorins in photodynamic therapy
Phlorins and oxophlorins
Phlorins
Oxophlorins
Corroles
Expanded systems: sapphyrins and pentaphyrins
Sapphyrins
Pentaphyrins
Porphycenes
Corrins
Biliverdins
Acknowledgements
Five-membered Monoheterocyclic Compounds - The Pyrrole Pigments (continued) / Chapter 13.:
Five-membered Monoheterocyclic Compounds: the Indigo Group / M. SainsburyChapter 14.:
Metal complexation
Photoisomerism and photochemistry of indigo, its derivatives and related compounds
Thermal isomerisation
Other indigo analogues
Oxidation and chemical reduction of indigo derivatives
Biosynthesis and the isolation of indigoids from natural sources
Cyanine Dyes and Related Compounds / G. Bach ; S. DahneChapter 15.:
Theory of color and constitution
The ideal polymethine state
Triad theory
Significance of NIR dyes
Progress in syntheses of cyanine dyes
Basic synthetic routes
Cyanines having halogeno and cyano substituents at the polymethine chain
Chain-bridged cyanines
Pyrylium, thiapyrylium, and selenapyrylium cyanines
Reactions of cyanine dyes
Properties of cyanine dyes
Physico-chemical properties in the ground state
Electronic structure
Energy levels
Solvatochromism and hydrophobicity
Properties of photoexcited states
Intermolecular interactions of cyanine dyes
Ion pair formation
Homomolecular aggregation of cyanine dyes
Heteromolecular interaction of cyanine dyes
Applications of cyanine dyes
Analytical markers, probes, and sensors in chemistry and molecular biology
Probing solvent polarity and solvent hydrophobicity
Ion recognition
Fluorescence labeling in molecular biology
Cyanine dyes for probing physico-chemical properties of organized media
Structure of interfaces and Langmuir Blodgett (LB) layers
Probing dielectric constants, lipophilicity, and microviscosity
Determination of critical micelle concentration (cmc)
Determination of membrane potentials
Excitation energy transfer
Cyanine dyes in laser technology
Application of light induced polarization. Nonlinear optical properties
Applications of (photo)electrical and photochemical activity
Spectral sensitization
Photoinduced electron transfer (PET)
Photovoltaic and solar cells, solar collectors
Optical recording
Charge control agents for electrophotographic processes
Electroluminescence
Electronic photography
Application of cyanine dyes in molecular biology and medicine
Probing transport phenomena
Identification of active oxygen species
Photodynamic therapy by singlet oxygen generation through cyanine dyes
Guide to the Index
Contributor
Preface
List of common abbreviations and symbols used
5.

図書

図書
出版情報: Berlin : Springer, 1944-1963  v. ; 26 cm
シリーズ名: Handbuch der analytischen Chemie / herausgegeben von R. Fresenius und G. Jander ; T. 2
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6.

図書

図書
Malte Henkel
出版情報: Berlin ; Tokyo : Springer, c1999  xvii, 417 p. ; 25 cm
シリーズ名: Texts and monographs in physics
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Critical Phenomena: a Reminder / 1:
Phase Diagrams and Critical Exponents / 1.1:
Scale Invariance and Scaling Relations / 1.2:
Some Simple Spin Systems / 1.3:
Ising Model / 1.3.1:
Tricritical Ising Model / 1.3.2:
q-States Potts Model / 1.3.3:
Vector Potts Model / 1.3.4:
XY Model / 1.3.5:
Yang-Lee Edge Singularity / 1.3.6:
Percolation / 1.3.7:
Linear Polymers / 1.3.8:
Restricted Solid-On-Solid Models / 1.3.9:
Some Experimental Examples / 1.4:
Correspondence Between Statistical Systems and Field Theory / 1.5:
Correspondence of Physical Quantities / 1.6:
Free Energy Density / 1.6.1:
Correlation Functions / 1.6.2:
Correlation Lengths / 1.6.3:
Conformal Invariance / 2:
From Scale Invariance to Conformal Invariance / 2.1:
Conformal Transformations in d Dimensions / 2.2:
Conformal Transformations in Two Dimensions / 2.3:
Conformal Invariance in Two Dimensions / 2.4:
Correlation Functions of Quasi-primary Operators / 2.5:
The Energy-Momentum Tensor / 2.6:
Finite-Size Scaling / 3:
Statistical Systems in Finite Geometries / 3.1:
Finite-Size Scaling Hypothesis / 3.2:
Universality / 3.3:
Phenomenological Renormalization / 3.4:
Consequences of Conformal Invariance / 3.5:
Comparison with Experiments / 3.6:
Representation Theory of the Virasoro Algebra / 4:
Verma Module / 4.1:
Hilbert Space Structure / 4.2:
Null Vectors / 4.3:
Kac Formula and Unitarity / 4.4:
Minimal Characters / 4.5:
Correlators, Null Vectors and Operator Algebra / 5:
Null Vectors and Correlation Functions / 5.1:
Operator Algebra and Associativity / 5.2:
Analyticity and the Monodromy Problem / 5.3:
Riemann's Method / 5.4:
Ising Model Correlators / 6:
Spin-Density Four-Point Function / 6.1:
Energy-Density Four-Point Function / 6.2:
Mixed Four-Point Functions / 6.3:
Semi-Local Four-Point Functions / 6.4:
Coulomb Gas Realization / 7:
The Free Bosonic Scalar Field / 7.1:
Screened Coulomb Gas / 7.2:
Minimal Correlation Functions / 7.3:
Minimal Algebras and OPE Coefficients / 7.4:
The Hamiltonian Limit and Universality / 8:
Hamiltonian Limit in the Ising Model / 8.1:
Hubbard-Stratonovich Transformation / 8.2:
Hamiltonian Spectrum and Conformal Invariance / 8.3:
Temperley-Lieb Algebra / 8.5:
Laudau-Ginzburg Classification / 8.6:
Numerical Techniques / 9:
Simple Properties of Quantum Hamiltonians / 9.1:
Some Further Physical Quantities and their Critical Exponents / 9.2:
Translation Invariance / 9.3:
Diagonalization / 9.4:
Extrapolation / 9.5:
VBS Algorithm / 9.5.1:
BST Algorithm / 9.5.2:
The DMRG Algorithm / 9.6:
Conformal Invariance in the Ising Quantum Chain / 10:
Exact Diagonalization / 10.1:
General Remarks / 10.1.1:
Jordan-Wigner Transformation / 10.1.2:
Diagonalization of a Quadratic Form / 10.1.3:
Eigenvalue Spectrum and Normalization / 10.1.4:
Character Functions
Finite-Size Scaling Analysis / 10.2:
Ground State Energy / 10.3.1:
Operator Content / 10.3.2:
Finite-Size Corrections / 10.3.3:
Finite-Size Scaling Functions / 10.3.4:
The Spin I Quantum Chain / 10.3:
The Virasoro Generators / 10.4:
Recapitulation / 10.5:
Modular Invariance / 11:
The Modular Group / 11.1:
Implementation for Minimal Models / 11.2:
Modular Invariance at c =1 / 11.3:
Circle or Coulomb Models / 11.3.1:
Orbifold Models / 11.3.2:
Lattice Realizations / 11.4:
Further Developments and Applications / 12:
Three-States Potts Model / 12.1:
Supersymmetry and Superconformal Invariance / 12.2:
Ashkin Teller Model / 12.3:
Relation with the XXZ Quantum Chain / 12.4.1:
Global Symmetry and Boundary Conditions / 12.4.2:
Phase Diagram / 12.4.3:
Operator Content on the c =1 Line / 12.4.4:
XXZ Quantum Chain / 12.5:
Ising Correlation Functions on Cylinders / 12.7:
Alternative Realizations of the Conformal Algebra / 12.8:
Logarithmic Conformal Theories / 12.8.1:
Lattice Two-Point Functions / 12.8.2:
Polymers / 12.9:
Lattice Animals / 12.10.1:
A Sketch of Conformal Turbulence / 12.11:
Some Remarks on 3D Systems / 12.12:
Conformal Perturbation Theory / 13:
Correlation Functions in the Strip Geometry / 13.1:
General Remarks on Corrections to the Critical Behaviour / 13.2:
Tower of the Identity / 13.3:
Application to the Ising Model / 13.3.2:
Application to the Three-States Potts Model / 13.3.3:
Checking the Operator Content from Finite-Size Corrections / 13.3.4:
Ising Model: Thermal Perturbation / 13.4:
Ising Model: Magnetic Perturbation / 13.4.2:
Truncation Method / 13.5:
The Vicinity of the Critical Point / 14:
The c-Theorem / 14.1:
Application to Polymers / 14.1.1:
Conserved Currents Close to Criticality / 14.2:
Exact S-Matrix Approach / 14.3:
Phenomenological Consequences / 14.4:
Integrable Perturbations / 14.4.1:
Universal Critical Amplitude Ratios / 14.4.2:
Chiral Potts Model / 14.4.3:
Oriented Interacting Polymers / 14.4.4:
Non-integrable Perturbations / 14.4.5:
Asymptotic Finite-Size Scaling Functions / 14.5:
Surface Critical Phenomena / 15:
Systems with a Boundary / 15.1:
Conformal Invariance Close to a Free Surface / 15.2:
Finite-Size Scaling with Free Boundary Conditions / 15.3:
Surface Operator Content / 15.4:
Temperley-Lieb Algebra and Relation with the XXZ Chain / 15.4.1:
Ashkin-Teller Model / 15.4.4:
Profiles / 15.4.7:
Defect Lines
Aperiodically Modulated Systems / 15.6.1:
Persistent Currents in Small Rings / 15.6.2:
Strongly Anisotropic Scaling / 16:
Dynamical Scaling / 16.1:
Schrödinger Invariance / 16.2:
Towards Local Scale Invariance for General ? / 16.3:
Some Remarks on Reaction-Diffusion Processes / 16.4:
Anhang/Annexe
List of Tables
List of Figures
References
Index
Critical Phenomena: a Reminder / 1:
Phase Diagrams and Critical Exponents / 1.1:
Scale Invariance and Scaling Relations / 1.2:
7.

図書

図書
edited by Egon Matijević
出版情報: New York, N.Y. : Plenum Press, c1976-  v. ; 24 cm
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Physical Chemistry of Cetyl Alcohol: Occurrence and Function of Liquid Crystals in O/W Creams / Shoji Fukushima ; Michihiro Yamaguchi1.:
Introduction
Cetyl Alcohol
Description of Cetyl Alcohol / 1.1.:
Short History of Cetyl Alcohol / 1.2.:
Definitions in Official Books / 1.3.:
Physical Properties of Cetyl Alcohols / 2.:
Polymorphism of Higher Alcohols / 2.1.:
Crystal Structure of Higher Alcohols / 2.2.:
Melting Point and Transition Point of Higher Alcohols / 2.3.:
Transition Point and Infrared Absorption / 2.4.:
Specific Interaction between 1-Hexadecanol and 1-Octadecanol / 3.:
Composition of Commercially Available Cetyl Alcohol / 3.1.:
Transition Point of 1-Hexadecanol / 3.2.:
Interaction between Higher Alcohols and Water / 4.:
Experimental Facts / 4.1.:
Formation of Hemihydrate / 4.2.:
Structure of Hydrated Alcohols / 4.3.:
Phase Diagram of the 1-Hexadecanol/1-Octadecanol/Water Ternary System / 4.4.:
Studies on Higher Alcohol/Surfactant/Water Systems / 5.:
The 1-Decanol/Sodium Caprylate/Water System / 5.1.:
The 1-Hexadecanol/OTAC/Water System / 5.2.:
Rheology of Ternary Systems Containing 1-Hexadecanol or a Homologous Alcohol / 5.3.:
Influence of the Amount of 1-Hexadecanol / 5.3.1.:
Influence of the Nature of Surfactant and of Higher Alcohol / 5.3.2.:
Influence of Alkyl Chain Length of Surfactant / 5.3.3.:
Conclusion / 5.3.4.:
Nature of Ternary Systems Prepared with Hexaoctadecanols / 6.:
Stability and Rheological Properties of Ternary Systems as a Function of Temperature / 6.1.:
Variations in External Appearance / 6.1.1.:
Variations in Viscosity / 6.1.2.:
Microscopic Observation / 6.1.3.:
X-Ray Diffraction Analysis / 6.1.4.:
Low-Angle X-Ray Diffraction Analysis / 6.1.5.:
Thermal Property / 6.1.6.:
Polymorphism of Hexaoctadecanol (3:2) and Stability of a Ternary Cream / 6.2.:
Liquid Crystalline Phases in Hexaoctadecanol (3:2)/Surfactant/Water Ternary Systems / 7.:
Phase Diagram / 7.1.:
D[subscript 2] Region / 7.2.:
M Region / 7.3.:
The Location and State of the D[subscript 2] Phase and M Particles in a Ternary Cream / 7.4.:
Temperature and the Process Yielding the Liquid Crystalline Phase / 8.:
Temperature of the Formation of the Liquid Crystalline Phase / 8.1.:
Method of Phase Separation Experiments / 8.1.1.:
Results of the Phase Separation Experiment / 8.1.2.:
G Phase and S Phase / 8.2.:
X-Ray Diffraction / 8.2.1.:
Differential Scanning Calorimetry / 8.2.3.:
Temperature at which the LC Phase is Formed / 8.2.4.:
In situ Formation of G and M Phases / 8.3.:
The Function of Liquid Crystalline Phases in O/W Creams / 9.:
Studies on O/W Creams / 9.1.:
The Difference in the Viscosity-Increasing Effects due to the Nature of Higher Alcohols / 9.2.:
The Difference in the Viscosity-Increasing Effect due to the Nature of Surfactants / 9.3.:
The Viscosity Change due to the Ratio of Cetostearyl Alcohol to Surfactant / 9.4.:
The Effect of Mixing 1-Hexadecanol with 1-Octadecanol / 9.5.:
Crystallization of Cetyl Alcohol in Cosmetic Creams / 9.6.:
Internal Structure and Stability of O/W C Creams / 10.:
Internal Structure of O/W Creams / 10.1.:
A Novel Theory for the Stabilization of O/W Creams / 10.2.:
Additional References on Cetyl and Homologous Alcohols / Appendix 1:
Appendix 2
References
Ionization Processes and Proton Binding in Polyprotic Systems: Small Molecules, Proteins, Interfaces, and Polyelectrolytes / Michael Borkovec ; Bo Jonsson ; Ger J. M. Koper
Experimental Techniques
Macroscopic Techniques
Definition and Measurement of pH / 2.1.1.:
Potentiometric Titration Techniques / 2.1.2.:
Other Macroscopic Techniques / 2.1.3.:
Spectroscopic Methods
Nuclear Magnetic Resonance (NMR) Techniques / 2.2.1.:
Optical and Other Spectroscopic Methods / 2.2.2.:
Modeling of Ionizable Systems
General Considerations
Computer Simulation Techniques
Simple Electrolyte Solutions / 3.3.:
Poisson-Boltzmann (PB) and Debye-Huckel (DH) Approximations / 3.3.1.:
An Illustrative Example / 3.3.2.:
Beyond the Poisson-Boltzmann (PB) Approximation / 3.3.3.:
Charged Molecules and Macromolecules in Water / 3.4.:
Debye-Huckel (DH) and Poisson-Boltzmann (PB) Treatment / 3.4.1.:
High-Salt versus Low-Salt Regime / 3.4.2.:
Toward Detailed Molecular Models / 3.4.3.:
Treatment of Ionization Equilibria / 3.5.:
Single Ionizable Site / 3.5.1.:
Localized versus Delocalized Binding / 3.5.2.:
Macroscopic Description / 3.5.3.:
Microscopic Description / 3.5.4.:
Adding Internal Degrees of Freedom / 3.5.5.:
Small Molecules
Monoprotic Acids and Bases
Equilibrium Constants / 4.1.1.:
Titration Behavior / 4.1.2.:
Experimental Data / 4.1.3.:
Diprotic Acids and Bases
Conformational Degrees of Freedom / 4.2.1.:
Equivalent Sites / 4.2.4.:
Oligoprotic Acids and Bases
Microscopic Description for Triprotic Acids and Bases / 4.3.1.:
Linear Molecules / 4.3.3.:
Noninteracting Sites
Microscopic versus Macroscopic Picture / 4.4.1.:
Affinity Distributions / 4.4.2.:
Interpretation and Prediction of Ionization Constants / 4.5.:
Empirical Methods / 4.5.1.:
Methods Based on First Principles / 4.5.2.:
Proteins
The Null Model
The Smeared-Out Charge Model
The Tanford-Kirkwood Model
Solution Techniques of the Ionization Problem
Shifts in Ionization Constants
Recent Developments in Dielectric Continuum Models / 5.4.:
General Methodology / 5.4.1.:
Case Studies / 5.4.2.:
Side Chain Flexibility / 5.4.3.:
Beyond Dielectric Continuum Models / 5.5.:
Protein Folding / 5.6.:
Polyelectrolytes
Mean-Field Models
Nearest-Neighbor Chain Interaction Models
Discrete Charge Model / 6.3.:
Mean-Field and Smearing-Out Approximations / 6.3.1.:
Chain Flexibility / 6.3.2.:
Polyamines / 6.4.:
Linear Polyamines / 6.4.1.:
Branched Polyamines / 6.4.2.:
Polycarboxylates / 6.5.:
Weakly Charged Linear Polycarboxylates / 6.5.1.:
Highly Charged Linear Polycarboxylates / 6.5.2.:
Humic Acids / 6.6.:
Ionizable Interfaces
Diffuse Layer Model and Its Generalization
Nernstian Surface / 7.1.1.:
Basic Stern Model / 7.1.2.:
Specific Counterion Binding / 7.1.3.:
Smearing-Out Approximation / 7.2.1.:
1-pK versus 2-pK Models / 7.2.2.:
pK Shifts / 7.2.3.:
Latex Particles
Ionizable Monolayers
Metal Oxide and Metal Hydroxide Particles / 7.5.:
Experimental Aspects / 7.5.1.:
Data Interpretation / 7.5.2.:
Goethite / 7.5.3.:
Hematite / 7.5.4.:
Rutile and Anatase / 7.5.5.:
Gibbsite / 7.5.6.:
Silica / 7.5.7.:
Discussion
Electrostatics of Point Charges / Appendix A.:
Planar Interface / A.1.:
Sphere / A.2.:
Cylinder / A.3.:
Further Tools in the Ising Model Analysis / Appendix B.:
Cluster Expansion / B.1.:
Other Choices of State Variables / B.2.:
Mean-Field Cluster Expansions / B.3.:
Mean-Field Treatment of Nonequivalent Sites / B.4.:
Square Lattice with Nearest-Neighbor Interactions / B.5.:
Affinity Distribution Approach / Appendix C.:
Derivation from Simple Models / C.1.:
Experimental Data Inversion / C.2.:
Combined Application of Radiochemical and Electrochemical Methods for the Investigation of Solid/Liquid Interfaces / Kalman Varga ; Gabor Hirschberg ; Pal Baradlai ; Melinda Nagy
On the Significance of Radiotracer Methods in Sorption Studies
General Problems of Radioactive Contamination Studies
An Overview of Radiotracer Methods
Methods Used for the Investigation of Interfacial Phenomena
Experimental Techniques: A Historical Survey
Recent Progress
Methods Used for the Investigation of Radioactive Contamination-Decontamination of Constructional Materials
Selected Results
Adsorption of Anions and Cations on Polycrystalline Gold
Comparative Study of Specific Adsorption of Cl[superscript -], HSO[superscript - subscript 4]/SO[superscript 2- subscript 4] and HSO[superscript - subscript 3]/SO[superscript 2- subscript 3] Ions / 3.1.1.:
Electrosorption of Ag and Co Species / 3.1.2.:
Accumulation of [superscript 110m]Ag on an Austenitic Stainless Steel
Sorption Behavior of Duplex Stainless Steels in HCl and H[subscript 2]SO[subscript 4] Solutions
Time and Concentration Dependence of Cl[superscript -] and HSO[superscript - subscript 4]/SO[superscript 2- subscript 4] Accumulations
Potential Dependence of Cl[superscript -] and HSO[superscript - subscript 4]/SO[superscript 2- subscript 4] Accumulations
Conclusions
Author Index
Subject Index
Magnetic Particles: Preparation, Properties and Applications / M. Ozaki1:
Maghemite (gamma-Fe2O3): A Versatile Magnetic Colloidal Material / C.J. Serna ; M.P. Morales2:
Dynamics of Adsorption and Oxidation of Organic Molecules on Illuminated Titanium Dioxide Particles Immersed in Water / M.A. Blesa ; R.J. Candal ; S.A. Bilmes3:
Colloidal Aggregation in Two-Dimensions / A. Moncho-Jorda ; F. Martinez-L=pez ; M.A. Cabrerizo-V8lchez ; R. Hidalgo Alvarez ; M. Quesada-PMFrez4:
Kinetics of Particle and Protein Adsorption / Z. Adamczyk5:
Physical Chemistry of Cetyl Alcohol: Occurrence and Function of Liquid Crystals in O/W Creams / Shoji Fukushima ; Michihiro Yamaguchi1.:
Introduction
Cetyl Alcohol
8.

図書

図書
Edited by Tsoo E. King, Howard S. Mason [and] Martin Morrison
出版情報: New York : Wiley, [1965]  2 v. (xxiv, 1144 p.) ; 24 cm
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図書

図書
David Hume ; introduction by A.D. Lindsay
出版情報: London ; Toronto : J.M. Dent , New York : Dutton, 1911  2 v. ; 18 cm
シリーズ名: Everyman's library ; no. 548-549 . Philosophy and theology
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Introductory Material / Part 1:
How to Use this Book
List of Abbreviations
Editor's Introduction Hume's Early years and Education
A Treatise of Human Nature
Of the Understanding / Book 1:
The Elements of the Mental World / Book 1 part 1:
The Ideas of Space and Time / Book 1 Part 2:
Knowledge, Probability, Belief, and Causation / Book 1 Part 3:
Forms of Scepticism / Book 1 Part 4:
Of the passions / Book 2:
The Indirect Passions of Pride and Humility / Book 2 Part 1:
The Indirect Passions of Love and Hatred / Book 2 Part 2:
The Direct Passions and the Will / Book 2 part 3:
Of Morals / Book 3:
The Source of Moral Distinctions / Book 3 Part 1:
The Artificial Virtues / Book 3 Part 2:
Natural Virtues and Natural Abilities The Abstract and the Early Reception of the Treatise Supplementary Reading A Note on the Texts of this Edition / Book 3 Part 3:
The Text / Part 2:
Advertisement
Introduction
Of ideas, their origin, composition, connexion, abstraction, etc.
Of the origin of our ideas / Sect. 1:
Division of the subject / Sect. 2:
Of the ideas of the memory and imagination / Sect. 3:
Of the connexion of association of ideas / Sect. 4:
Of relations Sect. 6 Of modes and substances / Sect. 5:
Of abstract ideas / Sect. 7:
Of ideas of space and time
Of the infinite divisibility of our ideas of space and time
Of the infinite divisibility of space and time
Of the other qualities of our ideas of space and time
Objections answered
The same subject continued
Of the idea of existence and of external existence / Sect. 6:
of knowledge and probability / Part 3:
Of knowledge
Of probability; and of the idea of cause and effect
Why a cause is always necessary
Of the component parts of our reasonings concerning cause and effect
Of the impressions of the senses and memory
Of the inference from the impression to the idea / Section. 6:
Of the nature of the idea or belief
Of the causes of belief / Sect. 8:
Of the effects of other relations and other habits / Sect. 9:
Of the influence of belief / Sect 10:
Of the probability of chances / Sect. 11:
Of the probability of causes / Sect. 12:
Of unphilosophical probability / Sect. 13:
Of the idea of necessary connexion / Sect. 14:
Rules by which to judge of causes and effects / Sect. 15:
Of the reason of animals / Sect. 16:
Of the sceptical and other systems of philosophy / Part 4:
Of scepticism with regard to reason
Of scepticism with regard to the senses
Of the ancient philosophy
Of the modern philosophy / Sect 4:
Of the immateriality of the soul
Of personal identity
Conclusion of this book
Of the Passions
Of pride and humility
Of pride and humility; their objects and causes
Whence these objects and causes are derived
Of the relations of impressions and ideas
Of the influence of these relations on pride and humility
Limitations of this system
Of vice and virtue
Of beauty and deformity <
Introductory Material / Part 1:
How to Use this Book
List of Abbreviations
10.

図書

図書
Editors: G. W. Gray, P. A. Winsor
出版情報: Chichester, Eng. : E. Horwood , New York : Halsted Press, 1974  v. ; 24 cm
シリーズ名: Ellis Horwood series in physical chemistry ; . Liquid crystals & plastic crystals ; v. 1-2
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図書
von Gustav Doetsch
出版情報: Basel : Birkhäuser, 1955-1956  2 v. ; 25 cm
シリーズ名: Lehrbücher und Monographien aus dem Gebiete der exakten Wissenschaften ; Mathematische Reihe ; Bd. 15,19 . Handbuch der Laplace-Transformation ; Bd. 2-3
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図書
H. Dean Baker, E.A. Ryder, N.H. Baker
出版情報: New York : J. Wiley , London : Chapman & Hall, c1953-c1961  2 v. ; 24 cm
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図書
computed and compiled under the direction of Harold T. Davis
出版情報: Bloomington : Principia Press, c1933-c1935  2 v. ; 25 cm
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図書
小平吉男著
出版情報: 東京 : 文献社 , 東京 : 現代工学社 (発売), 1971.10  2冊 ; 22cm
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図書
小西一郎, 横尾義貫, 成岡昌夫共著
出版情報: 東京 : 丸善, 1951.9-1963.3  2冊 ; 22cm
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16.

図書

図書
I.M.ヴォロンコウ [ほか] 著 ; 清野節男訳
出版情報: 東京 : 東京図書, 1963  2冊 ; 22cm
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17.

図書

図書
by Arthur W. Judge
出版情報: London : Sir Isaac Pitman, 1930 - 1932.  v. ; 22 cm
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目次情報:
v. 1. Ferrous
v. 2. Non-ferrous metals and organic materials
v. 3. Theory and testing of materials
v. 1. Ferrous
v. 2. Non-ferrous metals and organic materials
v. 3. Theory and testing of materials
18.

図書

図書
edited by Lawrence J. Berliner
出版情報: New York : Academic Press, 1976-1979  2 v. ; 24 cm
シリーズ名: Molecular biology : an international series of monographs and textbooks
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19.

図書

図書
柴田和雄, 今村昌, 池上明編著
出版情報: 東京 : 学会誌刊行センター , 東京 : 学会出版センター (発売), 1978.4-1981.12  3冊 ; 22cm
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20.

図書

図書
Hrsg. von G. -M. Schwab ; bearbeitet von F. Adickes ... [et al.]
出版情報: Wien : Springer, 1943  2 v. , p. ; 25 cm
シリーズ名: Handbuch der Katalyse / herausgegeben von G.-M. Schwab ; Bd. 7
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21.

図書

図書
佐藤竺, 西原道雄共編
出版情報: 東京 : 有斐閣, 1969.6-1969.11  2冊 ; 22cm
シリーズ名: 現代行政シリーズ ; 1-2
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22.

図書

図書
edited by G.N. Ramachandran
出版情報: London ; New York : Academic P., 1967  2 v ; 24 cm
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23.

図書

図書
堀健夫著
出版情報: 東京 : みすず書房, 1952.5-1953.6  2冊 ; 22cm
シリーズ名: 物理学大系 ; 基礎物理篇 6
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24.

図書

図書
edited by E.W. McDaniel, M.R.C. McDowell
出版情報: Amsterdam : North-Holland, 1969-1974  4 v. ; 22 cm
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25.

図書

図書
E. B. Jones
出版情報: London : Butterworths Scientific Pub., 1953-1957  v. ; 26 cm
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目次情報:
v. 1 : Measurement of pressure, level, flow and temperature
vol. 2 : Analysis instruments
vol. 3 : Telemetering and automatic control
v. 1 : Measurement of pressure, level, flow and temperature
vol. 2 : Analysis instruments
vol. 3 : Telemetering and automatic control
26.

図書

図書
エリ・ランダウ, イェ・リフシッツ著 ; 井上健男, 安河内昂, 佐々木健訳
出版情報: 東京 : 東京図書, 1962.9-1965  2冊 ; 22cm
シリーズ名: ランダウ=リフシッツ理論物理学教程
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27.

図書

図書
椿東一郎著
出版情報: 東京 : 森北出版, 1973-1974  2冊 ; 22cm
シリーズ名: 基礎土木工学全書 ; 6, 7
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28.

図書

図書
E.S.クェイド, W.I.ブッチァー編 ; 香山健一, 公文俊平訳
出版情報: 東京 : 竹内書店, 1972  2冊 ; 27cm
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29.

図書

図書
佐野敏一, 高木宣昭, 竹内守共著
出版情報: 東京 : オーム社, 1987  2冊 ; 22cm
シリーズ名: 絵とき電子回路シリーズ ; 2-3
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30.

図書

図書
edited by W. A. Krivsky
出版情報: New York : Gordon and Breach, [1965-1966]  2 v. ; 24 cm
シリーズ名: Metallurgical Society conferences ; v. 34, pt. 1, 2
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31.

図書

図書
The Society of Dyers and Colourists, Bradford, Eng. (Yorkshire)
出版情報: Bradford : Society of Dyers and Colourists , Lowell, Mass. : American Association of Textile Chemists and Colorists, c1956-  v. ; 28 cm
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32.

図書

図書
editor, Donald M. Ginsberg
出版情報: Singapore ; Teaneck : World Scientific, c1989-c1996  5 v. ; 23 cm
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33.

図書

図書
edited by Julian F. Johnson, Roger S. Porter
出版情報: New York : Plenum Press, 1970-  v. ; 26cm
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34.

図書

図書
C.シュヴァレー著 ; 銀林浩訳
出版情報: 東京 : 東京図書, 1975.9  2冊 ; 22cm
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35.

図書

図書
緒方章著
出版情報: 東京 : 南江堂, 1957-1966  7冊 ; 27cm
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36.

図書

図書
コスミンスキー著 ; 阿部玄治訳
出版情報: 東京 : 未来社, 1957.4-1961.1  5冊 ; 22cm
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37.

図書

図書
edited by A.F. Metherell, H.M.A. El-Sum, and Lewis larmore
出版情報: New York : Plenum Press, 1969-c1977  v. ; 26 cm
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38.

図書

図書
吉本隆明著
出版情報: 東京 : 勁草書房, 1965.5-1965.10  2冊 ; 20cm
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39.

図書

図書
edited by W.Y. Cheung
出版情報: New York ; Tokyo : Academic Press, 1980-1987  v. ; 24 cm
シリーズ名: Molecular biology : an international series of monographs and textbooks
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目次情報:
v. 1. Calmodulin
v. 1. Calmodulin
40.

図書

図書
C.G.Overberger編 ; 湊宏訳
出版情報: 東京 : 東京化学同人, 1969.3  2冊 ; 22cm
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41.

図書

図書
И.Л. Кнунянц, главный редактор ... [и др.]
出版情報: Москва : Советская энциклопедия, 1961-1967  5 v. ; 27 cm
シリーズ名: Энциклопедии, словари, справочники
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42.

図書

図書
edited by J. F. Coetzee and Calvin D. Ritchie
出版情報: New York : Marcel Dekker, 1969-c1976  2 v. ; 24 cm
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43.

図書

図書
by C.E. Weatherburn
出版情報: Cambridge : Cambridge University Press, 1927-1930  2 v. ; 22 cm
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44.

図書

図書
出版情報: Berlin : Springer, 1940-1978  28 v. ; 26 cm
シリーズ名: Handbuch der analytischen Chemie / herausgegeben von R. Fresenius und G. Jander ; T. 3
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目次情報: 続きを見る
Bd. 1a. Elemente der Ersten Hauptgruppe : einschl. Ammonium : Lithium, Natrium, Kalium, Ammonium, Rubidium, Caesium / bearbeitet von E. Brennecke ... [et al.]
Bd. 2a. Elemente der Zweiten Hauptgruppe : Beryllium, Magnesium, Calcium, Strontium, Barium, Radium und Isotope / bearbeitet von F. Busch ... [et al.]
Bd. 2b. Elemente der Zweiten Nebengruppe : Zink, Cadmium, Quecksilber / bearbeitet von Herbert Funk ... [et al.]
Bd. 5b. Elemente der fünften Nebengruppe : Vanadin, Niob, Tantal / bearbeitet von G. J. van Kolmeschate
Bd. 8a. Elemente der Achten Hauptgruppe : Edelgase : Helium, Neon, Argon, Krypton, Xenon, Radon und Isotope / bearbeitet von H. Kahle, B. Karlik
Bd. 1a. Elemente der Ersten Hauptgruppe : einschl. Ammonium : Lithium, Natrium, Kalium, Ammonium, Rubidium, Caesium / bearbeitet von E. Brennecke ... [et al.]
Bd. 2a. Elemente der Zweiten Hauptgruppe : Beryllium, Magnesium, Calcium, Strontium, Barium, Radium und Isotope / bearbeitet von F. Busch ... [et al.]
Bd. 2b. Elemente der Zweiten Nebengruppe : Zink, Cadmium, Quecksilber / bearbeitet von Herbert Funk ... [et al.]
45.

図書

図書
edited by E. Anthony Evans and Mitsuo Muramatsu
出版情報: New York : M. Dekker, c1977  2 v. (xiii, 1211 p.) ; 24 cm
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46.

図書

図書
B.R. Lazarenko
出版情報: New York : Consultants Bureau, 1964-1965  3 v. ; 27 cm
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47.

図書

図書
Johannes R. Becher
出版情報: Berlin : Aufbau-Verlag, 1952  v. ; 20 cm
シリーズ名: Auswahl in sechs Bänden ; Bd. 1-3
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48.

図書

図書
朝尾直弘 [ほか] 編集委員
出版情報: 東京 : 岩波書店, 1975.5-1977.6  26冊 ; 22cm
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49.

図書

図書
by W.V.D. Hodge and D. Pedoe
出版情報: Cambridge : Cambridge University Press, 1947-1954  3 v. ; 23 cm
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50.

図書

図書
中善寺, 登喜次(1911-)
出版情報: 東京 : 彰国社, 1956-1957  2冊 ; 30cm
シリーズ名: 現代建築の詳細 / 中善寺登喜次著 ; 1,2
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