SUBJECT INDEX – VOLUME 79 (2005)
Inorganic and Physical Chemistry
ab initio calculations, 1223, 1873
absorption spectrum, 1805
acidity constants, 1251
activation parameters, 1689, 1813
adduct, 671, 1949
adsorption, 1205, 1513, 1787
adsorption isotherms, 1787
alloys, 1365
angular overlap model, 47
antimicrobial activity, 679, 1107, 1123, 1615, 1843
artificial neural network, 1565
association, 1503, 1937
atomic core, 1435
atomic coordinates, 1315
atomic force microscopy (AFM), 1205
Belousov-Zhabotinsky reaction, 135
bifurcation, 135
binary solvent mixtures, 1143, 1251
binary system, 1217, 1235
binding energy, 1365
biological activity, 1
biomimetic hydroxylation, 655
bond length, 31, 637, 655, 671, 1041, 1079, 1099, 1193, 1223, 1389, 1535, 1615
bond valence method, 31
capillary electrophoresis, 1565
catalysis heterogeneous, 121, 1357, 1495, 1821, 1963
catalysis homogeneous, 933
catalyst synthesis, 145, 655, 1963
catalytic conversion, 1821
charge transfer, 671, 1265, 1525, 1949
charge transfer coefficient, 1379
chelates, 619
chemosensors, 1721
chemometrics, 1251
chronoamperometry, 1327, 1379
chronocoulometry, 1327
classification of elements, 1435
colapse pressure, 773
complexes, 31, 619, 627, 637, 655, 671, 679, 807, 951, 959, 1041, 1099, 1115, 1123, 1143, 1389, 1445,
1585, 1597, 1615, 1713, 1739, 1829, 1843, 1853, 1873
complexes binuclear, 57, 1597, 1731, 1749
complexes heterobinuclear and heterotetranuclear, 31, 1265, 1405, 1415, 1425
complexes inclusion, 1461
computational electrochemistry, 1379
conductivity, 637, 645, 807, 817, 1115, 1123, 1143, 1265, 1415, 1585
conservation of paper, 1575
conversion of ammonia, 1495
conversion of hydrocarbons, 945, 1357, 1821
coordination polymer, 1835
coupled chemical reaction, 1327
crosslinking, 897
crystal field parameters, 1805
crystal structure, 31, 637, 655, 671, 759, 1079, 1099, 1193, 1315, 1389, 1535, 1835
cyclic voltammetry, 679, 1107, 1123, 1327, 1379, 1525, 1605, 1739
decomposition, 1495
dehydration, 1721
density functional theory, 1041, 1193, 1223
desorption, 1205
dielectric relaxation, 1353
differential capicity, 1513
diffusion, 759, 897, 907
diffusion-reaction systems, 759
dimerization, 1937
dimerization constant, 1235
dipole moment, 1047
discharge synthesis, 945
dissociation constant, 645, 1235
distribution diagram, 1251, 1445
distribution ratio, 1235, 1531
electric permittivity, 1513
electrical conductivity, 1135
electrochemistry, 1327, 1379
electron delocalization, 1093
electronic spectra, 37, 47, 129, 619, 663, 807, 817, 919, 959, 1041, 1115, 1123, 1251, 1265, 1405, 1415,
1425, 1445, 1525, 1605, 1635, 1689, 1731, 1749, 1843, 1937, 1949
electrooxidation, 1063
electrophoretic technique, 1853
electroreduction, 1063
equilibrium constants, 919, 1235, 1301, 1445, 1861
ESR spectra, 37, 145, 663, 679, 817, 1107, 1389, 1415, 1425, 1731, 1749
eutectics, 1033
excess function, 1503
excited states, 1873
ferromagnetic coupling, 37, 1415
fluid interfaces, 129
fluorescence, 1721
formal potential, 1379
formation constants, 1445, 1689, 1861
frequency domain, 1353
FTIR spectroscopy, 1399
fuell cells, 1063
fungicides, 1843
fuzzy k-nearest neighbour rule, 1365
gas chromatography, 883
guest molecules, 1835
harmonic oscillator model of aromaticity, 1093
heteroacids, 1813
high pressure, 783, 789, 1339
hydrides, 789,
hydrogel, 897
hydrogen bond, 1079, 1093, 1193, 1223, 1389, 1829
hydrolysis, 933
hydrothermal reaction, 1041
hydrothermal synthesis, 121, 1835
impedance, 1513
intermetallic compound, 1315
intermolecular interactions, 1223
ionic liquids, 1929
iridescent phases, 129
IR spectra, 37, 57, 619, 627, 637, 645, 655, 663, 671, 807, 817, 919, 951, 959, 1115, 1123, 1135, 1223,
1265, 1389, 1405, 1425, 1525, 1535, 1585, 1597, 1605, 1627, 1635, 1705, 1713, 1721, 1731,
1739, 1787, 1829, 1843, 1853
isomerization selectivity, 1821
isotherm, 773, 1047, 1513, 1787
isothermal section, 1315
isotope effect, 1813
kinetic energy, 1365
kinetics, 933, 1301, 1461, 1689, 1813
Langmuir monolayers, 773, 1047
ligand-field analysis, 47
liquid-liquid distribution, 1235
magnetic properties, 37, 47, 619, 679, 789, 817, 1107, 1115, 1123, 1265, 1389, 1405, 1415, 1425, 1585,
1739, 1749, 1835
mass spectrometry, 1123, 1597, 1605, 1705, 1949
melting diagram, 1033
micellar electrokinetic chromatography, 1565
micropolarity, 129
mixed solvents, 1143
molar volume, 1445
molecular orbital calculations, 1193
molecular structure, 31, 679, 1099, 1193, 1615, 1873
monolayer, 773
multiline approach, 1365
nanosilica, 1787
non-aqueous solvent, 1143
NMR, 57, 619, 627, 663, 817, 951, 1099, 1115, 1123, 1597, 1627, 1705, 1731, 1739
non-stoichiometry, 907
optical reflectance, 1135
oscillation, 135
oxidation, 1689, 1813
m-oxamido-bridge, 1405, 1415, 1425
oxide, 907
partition coefficient, 883, 1235
pattern recognition, 1365
penetration depth, 783
periodic system, 1435
permeability of oxygen, 1539
phase diagram, 1217, 1315, 1339
phase equilibria, 1033, 1339, 1503
photocatalyst, 919
photocatalysis, 1929
photochemical reactions, 1929
photodegradation, 919
pH titration, 1861
plasma, 945, 1539, 1957
polymeric system, 897
potential redox, 1063, 1087
potentiometric method, 645, 1787
protective coatings, 1575
protolytic constants, 1251
pulse voltammetry, 1327
Raman spectra, 1551
reaction mechanism, 933, 1963
recognition, 1365
recombination probability, 1205
redox properties, 1739
reduction, 1327
reflectance spectra, 1627
retention factor, 1565
scanning electron microscopy, 1575
Schiff base ligands, 47, 57, 619, 663, 959, 1107, 1123, 1327, 1535, 1597, 1843
segregation, 1365
semiconductor, 919
SERS, SERRS, 1551
single crystal, 1805
single molecule spectroscopy, 1551
solid-liquid equilibrium, 1339
solubility, 645, 1585, 1635, 1713
solubility Hildebrand coefficient, 1235
solvating ability, 1251
solvation, 1445
solvent effect, 1223
sorption, 759
spectral studies, 1115
surface segregation, 1365
stability, 1087
stability constants, 1461, 1531, 1853, 1861
standard potential, 1379
sticking probability, 1205
sticking coefficient, 1495
structure of complexes, 679, 1041, 1223
substituent effect, 883
superabsorbent, 897
surface charge, 1513, 1787
surface coverage, 1513
surface excess, 1513
surface potential, 1047
surface pressure, 773, 1047, 1513
surface tension, 1513
surfactant bilayers, 129
swelling behaviour, 897
synthesis complexes, 37, 57, 619, 627, 645, 671, 807, 951, 959, 1123, 1143, 1265, 1415, 1425, 1535,
1585, 1615, 1713, 1731, 1739, 1749, 1829
synthesis inorganic compounds, 637, 7759, 941, 959, 1099, 1193, 1389, 1399, 1705
tautomeric equilibria, 1093
template synthesis, 1597, 1627, 1731
ternary compounds, 1033, 1315
thermal analysis, 57, 619, 627, 645, 671, 959, 1033, 1217, 1399, 1525, 1585, 1605, 1635, 1713,
1835, 1843
thermal decomposition, 637, 959, 1079, 1635, 1713, 1721
thermodynamics, 783, 1357, 1379, 1461
thermodynamics properties, 1301, 1357
thermodynamics of complex formation, 1143, 1461, 1861
thin films, 1205
time domain, 1353
tip-enhanced Raman scattering, 1551
transfer coefficient, 1327, 1379
transition energy, 1873
transition metal compounds, 807
tripodal ligand, 1731
tungsten bronzes, 1135
vapour-liquid equilibrium, 1503
voltammetry, 1327, 1379
X-ray diffraction measurements, 121, 145, 655, 671, 919, 1033, 1099, 1135, 1193, 1315, 1399, 1575,
1635, 1713, 1721, 1835
X-ray photoelectron spectroscopy XPS, 145, 1365, 1957
zero charge potential, 1787
Organic Chemistry
Biologically active compounds
Acitenobacter species polysaccharides, 267
Aminobenzimidazoles, 709
Aminomethanediphosphonic acids, 445, 593
Anthracenediones, 1
Anthracyclines, 1, 335, 349
Antineoplastic agents, 1
Arginine vasopressin, 731
Brauhenefloroside C, 1883
Chalcones from Psoralea corylifolia, 1173
Clerodane diterpenoids, 1757
DNA binding, 831
Doxorubicin analogues, 349
Enzyme inhibitors, 583
Imidazoquinazolines, 89
Indoloquinolines, cytotoxicity, 369
Levorin A3, 1667
Limbatolide F, 1757
Limbatolide G, 1757
Nystatin A2, 1673
Peptide hormones, 731
Polysaccharides from Enterobacter sakazakii, 287
Sesquiterpenoids from Taraxacum rubicundum, 1547
Stachyfloroside E, 1295
Steroidal glycosides from Haloxylon salicornicum, 1469
Tanacetamide C, 967
Triazolobenzodithiazines, 1659
Vitamin D3, 413
Complexes, Organic Ligands of
Alkoxymethylaluminum, 1773
Cyclopentadienyl ligands, 1773
Phenols, 83
Polyoxaphosphonates, 699
Silicon podands, 717
Compounds (synthesis, reactions, and properties of)
Amines
Aminobenzimidazoles, 709
Daunosamine, 335
Hexamethylenetetramine, 1155
Hydroxylamines, 115
Guanidines, 401
Aminoacids and peptides
Alanine, L-, 1909
Aminopyroglutamic acid, 731
Glycopeptides, 297
Phosphonocysteine, 529
Phosphonocysteic acid, 529
Peptide hormones, 731
Aromatics
Nitroarenes, 163
Nitroporphyrins, 1169
Carboxylic acids and derivatives
Acetylenedicarboxylates, 845
Benzoyl isocyanide, 1189
Hydroxyacids, a-, 1179
Iminocarbonyl sulfenamides, 115
Ketoimides, 1901
Lactones, 1763
Lactones, d-, 239, 981
Mesitonitrile, N-oxide, 65
Ribonolactone, 323
Tanacetamide C, 967
Tetraamides, cyclic, 1909
Thiocarbamates, 329
Heterocycles
Adenosine crown ethers, 1781
Aminobenzimidazoles, 709
Benzothiazoles, 115
Imidazoles, 553
Imidazolium salts, 867
Imidazoquinazolines, 89
Indolizidines, 1919
Indoloquinolines, 369
Isatin, 845
Isoxazolines, 65
Oxazoles, 1889
Oxazolines, 721, 1015
Porphyrins, 1169
Pyrazilideneacetonitriles, 1275
Pyrazoloquinolines, 1645
Pyridones, 1919
Rhodanines, 1285
Tetrahydrothiophenes, 973
Triazines, 739
Triazolobenzodithiazines, 1659
Macrocycles
Azacrown compounds, 73
Bis-sulfonamides, macrocyclic, 223
Crown ethers, 73, 1781
Mannose based crown ethers, 211
Mannitol base crown ethers, 223
Tetraamides, cyclic, 1909
Threitol based crown ethers, 223
Nitro compounds
Nitroarenes, 163
Nitrones, 239
Nitroporphyrins, 1169
Organophosphorus, Organosulfur, Organoselenium, and Organosilicon Compounds
Alkoxyphosphonium salts, 473
Allylsilanes, 1919
Allyltin sugars, 231
Aminoalkylphosphonates, 445, 493, 499, 547, 553, 561, 573, 1895
Aminomethanediphosphonic acids, 445
Aminomethanediphosphonous acids, 525
Azidoalkylphosphonates, 493
Dialkyltin hydrides, 721
Oppolzer’s sultam, 1901
Phosphazenes, 493
Phosphine oxides, 541, 553
Phosphites, 487
Phosphitylation, 467
Phosphonocysteic acid, 529
Phosphonocysteine, 529
Phosphonohomocysteic acid, 529
Phosphonohomocysteine, 529
Polyoxaphosphonates, 699
Polyphosphonium compounds, 481
Selenophosphates, 515
Silicon podands, 717
Sulfenamides, 115
Thiadiazoles, 973
Thiiranes, 515
Thiocarbonyl ylides, 1483
Thiophosphates, 515
Tin hydrides, 1015
Trifluoromethylstannanes, 1187
Sugars
Allyltin sugars, 231
Deoxysugars, 1681
Galactopyranosides, 329
Galactouronates, 251
Glucopyranosides, 317
Glycals, 369
Glycopeptides, 297
Glycosides, 251, 329, 1295, 1469, 1883
Hexopyranoses, 335
Higher sugars, 231
Iminosugars, 239
Lypopolysaccharides, 267
Mannitol base crown ethers, 223
Mannose based crown ethers, 211
Mannooligosaccharides, 275
Mannopyranosides, 275
Ribose complexes, 323
Sugars, allyltin derivatives, 231
Threitol based crown ethers, 223
Trisaccharides, 1681
Terpenes and Steroids
Betulin, 361
Clerodane diterpenoids, 1757
Hexaterpenes, 429
Saponins, 361
Sarsapogenins, 1245
Steroidal glycosides, 1469
Organic Spectroscopy
Mass spectrometry of
Electrospray, 387, 1909
Rhodanines, 1285
Tetraamides, cyclic, 1909
NMR studies of
Alkoxymethylaluminum cyclopentadienyl complexes, 1773
Alkoxyphosphonium salts, 473
Aminophosphonic acids, 573
Brauhenefloroside C, 1883
Clerodane diterpenoids, 1757
Lactones, 1763
Oligosaccharides, 309
Pentasaccharides, 275
Phosphonocysteic acid, 529
Phosphonohomocysteic acid, 529
Phosphonohomocysteine, 529
Polysaccharides from Enterobacter sakazakii, 287
Tanacetamide C, 967
X-ray spectroscopy
Benzothiazoles, 115
Glycosides, 251
Lactones, 1763
Nitrones cycloadducts, 239
Oxazoles, 1889
Sulfenamides, 115
Reactions and Processes
Acylation, 217
Asymmetric synthesis, 1901, 1919
Bayer-Villiger oxidation, 1245
Chirality transfer, 561
Debenzylation, 317
Diastereoselection, 721, 1901
Diels-Alder reaction, 429
Dihalocarbene addition, 109
1,3-Dipolar cycloaddition, 65, 239, 973,1483
Electrooxidation, 1477
Glycosylation, 275, 297, 309, 329, 361
Horner-Wittig reaction, 541
Hydrostannation, 1015
Iodolactonization, 1763
Ionic liquids, 867
Keto-enol tautomerism, 689, 749, 1003
Ketonisation, catalytic, 995
Lactonization, 981
Michaelis-Arbuzov reaction, 473, 541
Nucleophilic substitution of hydrogen, oxidative, 163
Oligosaccharides synthesis, 309
Oxidation of alkylarenes, 825
Phase-transfer catalysis, 109
Phosphitylation, 467
Staudinger reaction, 493
Trifluoromethylation, 1187
Reviews
Aminomethanediphosphonic acids, 445
Anthracenediones, 1
Anthracyclines, 1
Liquid crystals, 179
Nucleophilic substitution of hydrogen, oxidative, 163