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図書
図書
1. Heterocyclic compounds. 2nd ed. (pt. A - pt. L. Suppl.)
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
2.

図書
図書
2. Surface and colloid science (v. 5 - v. 17)
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
3.

図書
図書
3. Physico-chemical properties and methods of investigation ([1] : E. Horwood - [2] : Halsted)
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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4.

図書
図書
4. Spin labeling : theory and applications ([1] ; 2)
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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5.

図書
図書
5. 太陽エネルギーの生物・化学的利用 ([1] ; 2 ; 3)
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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6.

図書
図書
6. 水理学 (1 ; 2 ; 2 [POD版])
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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7.

図書
図書
7. システム分析 (1 ; 2)
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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8.

図書
図書
8. 現代代数の基礎 (1 ; 2)
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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9.

図書
図書
9. Liquid crystals and ordered fluids ([Vol.1] - Vol. 4)
edited by Julian F. Johnson, Roger S. Porter
出版情報: New York : Plenum Press, 1970-  v. ; 26cm
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10.

図書
図書
10. Radiotracer techniques and applications (v. 1 ; v. 2)
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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