Polish Journal of Chemistry
SUBJECT INDEX VOLUME 75 (2001)
Inorganic and Physical Chemistry
ab initio calculations, 1483
activated carbons, 1913
activation parameters, 689, 965, 1051, 1229, 1729, 1739, 1745, 1775, 1895
adsorption, 93, 733, 857, 1493, 1561, 1913, 1927, 1947
bond length, 147, 299, 363, 1939
catalysis: heterogeneous, 283, 307, 733, 839, 857, 899, 1059, 1513, 1543, 1561, 1801, 1927
homogeneous, 869, 875
charge transfer, 1521, 1603
classification, 159, 1603
clay, 307
colloids, 571
complexes, 29, 35, 43, 147, 209, 215, 223, 299, 329, 337, 355, 363, 371, 379, 623, 689, 751, 755, 765, 773,
785, 879, 909, 941, 957, 965, 1063, 1067, 1081, 1195, 1203, 1219, 1367, 1387, 1393, 1533,
1591, 1597, 1689, 1695, 1703, 1711, 1781, 1785, 1791, 1817, 1825, 1833, 1887, 1905, 1947
conducting polymers, 1719, 1745, 1913
critical phenomena, 481, 557
crystal structure, 153, 299, 363, 453, 457, 633, 707, 751, 755, 765, 785, 879, 883, 899, 957, 1063, 1067,
1073, 1077, 1209, 1219, 1351, 1361, 1367, 1371, 1381, 1583, 1591, 1695, 1711,
1785, 1791, 1921
dielectric relaxation, 1505
diffusion, 501, 1001, 1051
dipole moment, 707, 845, 1521
electrical conductivity, 689, 759, 773, 941, 1195, 1229, 1703, 1745, 1817, 1913
electrode processes, 93, 1719
environment protection, 1543
high pressure, 1051, 1921
hydrides, 1051, 1921
intermetallic compound, 617
isotope effect, 115, 527, 889, 1333, 1729, 1921
kinetics, 79, 93, 105, 293, 571, 579, 699, 869, 949, 1019, 1059, 1229, 1333, 1513, 1729, 1739, 1775, 1801,
1895, 1947
lattice model, 1, 501, 527, 587
liquid crystals, 463, 1505
liquids, 481, 547, 557, 601
magnetic properties, 29, 215, 223, 299, 329, 355, 379, 773, 785, 795, 941, 957, 1067, 1195, 1203, 1229,
1401, 1417, 1689, 1695, 1703, 1711, 1817, 1825, 1833, 1921
model, 527, 557, 579, 601
oscillation, 443
oxidation, 283, 307, 869, 1019, 1333, 1513, 1905
periodic system, 159, 1603
phase diagram, 135, 453, 457, 463, 557, 617, 1077, 1407, 1413, 1553
phase separation, 517, 547, 579
phase transition, 1, 463, 547, 557, 617
proton transfer, 845, 1745, 1895
quantum calculations, 1039, 1569, 1603
reduction, 307
scaling laws, 587, 601
semiempirical methods, 371, 965, 1483, 1887
simulation, 517, 547, 587
solid state electrochemistry, 135, 1913
stability constants, 127, 345, 623, 905, 1081, 1533, 1887
surfactant, 1
synthesis: complexes, 29, 35, 43, 215, 223, 299, 329, 337, 355, 363, 371, 379, 623, 773, 785, 795, 879,
909, 941, 957, 965, 1063, 1067, 1081, 1195, 1203, 1219, 1387, 1393, 1401, 1591,
1689, 1695, 1703, 1711, 1781, 1817, 1825, 1833
inorganic compounds, 159, 719, 899, 1921
ternary compounds, 453, 457, 617, 633, 1073, 1077, 1583
thermal analysis, 43, 209, 299, 363, 719, 795, 909, 1209, 1393, 1401, 1407, 1413, 1781, 1927
thermodynamics, 135, 481, 905, 949, 965, 1081, 1341, 1493, 1553, 1767, 1797, 1853, 1887
viscosity, 115, 1505
voltammetry, 209, 699, 1219, 1493, 1597, 1719, 1745, 1753, 1781, 1887, 1913
Organic Chemistry
Biologically active compounds
Bovine b-trypsin inhibitors, 1863
Cyclolinopeptide A, 1441
Cytokine inducers, 657
Cysteine protease inhibitors, 831
Flavonoid aglycones from Scutellaria baicalensis, 1935
Hepatitis B virus antigen, 813
Human heat shock protein, 70(29-42) fragment, 265
Hydrazinecarbodithioic acid esters, tuberculostatic activity, 1237
Lactarorufin B, 1287
Lappaconitinecyclodextrine complex, 1297
Proctolin analogues, 411
Salsolidine, 1847
Saponin OSW-1 aglycone, 983
Somatostatin analogues, 1877
Sesquiterpene lactones from Picris evae, 141
Tryptamine, 5-hydroxy, receptor ligands, 71
Virucides inducers, 657
Complexes, Organic Ligands of
Antipyrine derivatives, Cu(II) complexes, 941
Aza-crown ethers, Ag(I) complexes, 345
Chrysin, Ti(IV), Fe(III), Co(II), Ni(II), Mn(II), and Cu(II) complexes, 795, 1401
Glutaric acid, 3,3-dimethyl, La(III) and Y(III) complexes, 43
Methylsuccinic acid, rare earth metals complexes, 1393
Nicotinamide, Co(II), Ni(II) and Zn(II) complexes, 371
Pentamethylenetetrazole, Co(II), Ni(II), and Cu(II) complexes, 1597
Phenanthroline, 1785
Phthalocyanine, Co(III) , 949
Pyrazoles, Cu(II) complex, 1381
Schiff bases, transition metal complexes, 29, 35
Tributyl phosphite, Cu(II) complexes, 215
Compounds (synthesis, reactions, and properties of)
Amines
Aminoazulenes, 275
Benzene, 1,2-diamine, Schiff bases, 35
Benzothiazole, 2-amino, Schiff bases, 29
Dioxotetraamines, metal complexes, 623
Diphenylamine, oxidation of, 1019
Guanidinium cation, 1839
Schiff bases, 29, 35, 79, 1475
Aminoacids and peptides
Antamanide, 1869
Bovine b-trypsin inhibitors, 1863
Cyclolinopeptide A, 1441
Cysteine derivatives, 831
Isoserinates, 1287
Phenylglycine derivatives, 411
Octapeptides, 1879
Aromatics
Aromatic disulphides, 895
Azobenzene, 4-amino, as chromophore group, 241
Azobenzenes, 699
Azoxybenzenes, 1839
Azulene, 275
Calixarenes, 921
Dihydroxynaphthalene derivatives, 1457
Paracyclophanes, 1351
Phthalocyanines, 949
Propellanes, 1881
Carboxylic acids and derivatives
Furan-2,5-dicarboxylic acid esters, 1943
Glutaric acid, 3,3-dimethyl, La(III) and Y(III) complexes, 43
Hydrazinecarbodithioic acid derivatives, 1237
Imidates, 975
Lactams, g- and d-, activity of, 1277
Pyruvates, condensation with phenol, 419
Thioamides, 387, 1303
Thiosters, 975
Ethers
Aza-crown ethers, Ag(I) complexes, 345
Crown ethers, 991, 1887, 1947
Propellanes, 1881
Tetrahydrofuran ring opening, 875
Tetraoxacyclophanes, 1247
Heterocycles
Azoles, C-phosphorylated, 1137
Azoles, nitro, 1474
1,4,2-Benzodithiazine, 1,1-dioxo, 1309
Benzothiazole, 2-amino, Schiff bases, 29
Benzofuranone, 419
Chromones, 63
Chrysin, Ti(IV), Fe(III), Mn(II) complexes, 795
Coumarin derivatives, 63
Cytisine, 1483
Flavonoid aglycones, 1935
Furan, aminophosphonic acids, 1271
Furan-2,5-dicarboxylic acid esters, 1943
Imidazoles, nitro derivatives, 639, 673, 1661
Isoquinolines, 1317
Nicotinamide, Co(II), Ni(II) and Zn(II) complexes, 371
Oxazolines, 1117
Oxazolones, ring opening, 401
Phthalocyanines, 949
Piperidineethanols, 1361
Pyrazoles, Cu(II) complex, 1381
Pyrazol-5-ones, 1367
Pyrrolecarbothioamides, 1853
Pyrimidines, 1039, 1661
Pyridine, 2,6-diacetyl, Schiff bases, 35
Pyridine, 2,6-dicarboxylates, 957
Pyridinium salts, solvatochromism of, 231
Purines, 1327,1661
Quinoline, 8-hydroxy, 623
Quinoline, 2-methyl-4-phenyl, formation of, 965
Tetrazoles, 253, 1597, 1869
Tetrazolium salts, 253
Thiazole, 4,5-dihydro derivatives, 387
Thiazolino[2,3-a]isoquinolinone, 1847
Thiophene, aminophosphonic acids, 1271
Triazole, 1,2,4-, 1475
Macrocycles
Aza-crown ethers, 345, 991
Calixarenes, 921
Chromoionophores, 1457
Cyclophanes, ferrocenylo, 677
Crown ethers from sugars, 683
Phthalocyanines, 949
Tetraoxacyclophanes, 1247
Nitro compounds
Benzene, 4-cyano-2,6-dinitro, derivatives, 1427
Bis(ethylsulfonyl)methane, 4-nitrophenyl-, 1895
2-Nitropentane, electroreduction of, 93
Nitroimidazoles, 639, 673, 1661
Nitroindazoles, 1465
Nitropyrazoles, 1465
Nucleosides, nucleotides, nucleic acids
DNA repair enzyme, 1183
Ribozymes, 1807
Organophosphorus, Organosulfur, Organoselenium, and Organosilicon Compounds
Aminophosphonic acids, 663, 1271
Azoles, C-phosphorylated, 1137
Bis(ethylsulfonyl)methane, 4-nitrophenyl-, 1895
Diselenobisbenzamides, 657
Diselenobisbutyramides, 657
Ebselen analogues, 823
Phosphonic acid, aminomethyl, 63
Phosphonoamides, cyclic, 1089
Phenylselenosodium, 649
Phenyltellurosodium, 649
Poly(alkylene phosphates), 1171
Thioamides, 1853
Selenophosphates, 1121
Sulfones, chloromethyl, 1465
Thiazolino[2,3-a]isoquinolinone, S-oxide, 1847
Thiophosphates, 1121
Thiocarbamates of monosaccharides, 1303
Sulfenic acid anilides, 895
Thiaphosphacyclanes, 1103
Tributyl phosphite, Cu(II) complexes, 215
Sugars
Carbohydrates, dithioacarbonic acid esters, 49
Carbohydrates, anomeric hydroxyl group replacement, 803
Cyclodextrin - lappaconitine complex, 1297
Monosaccharides, thiocarbamates of, 1303
Sucrose, 683
Sweetness of saccharides, 1569
Terpenes
Carvone, 55
Lactarorufin B, 1287
Ritter reaction of terpenes, 55
Sesquiterpenes from Picris evae, 141
Sesquiterpenes from Taraxacum bicorne, 1587
Taraxastane-type triterpenoid, 141
Mechanisms
Bis(ethylsulfonyl)methane, 4-nitrophenyl-, proton abstraction, 1895
Cine-substitution in nitroimidazoles, 639, 673
Methyl transfer in methylcobalt(III) phthalocyanine, 949
Quinoline formation, semiempirical calcuation, 965
Ring opening in oxazolones, 401
Ring opening of tetrahydrofuran, 875
Sigmatropic rearrangements, 649
Organic Spectroscopy
CD spectroscopy
Cyclolinopeptide A, 1441
EPR studies of
Antipyrine derivatives, Cu(II) complexes, 773, 941
NMR studies
31P, solid state, 1147
Mass spectrometry of
4-Iminopentan-2-ones, tautomerism of, 429
Reactions and Processes
Diphenylamine oxidation, 1019
Hydrogen transfer over magnesia, 1059
4-Iminopentan-2-ones, tautomerism of, 429
Reduction of ketones, 1059
Ritter reaction of terpenes, 55
Vicarious nucleophilic substitution, 275, 1465, 1661
Reviews
Azoles, C-phosphorylated, 1137
Calixarenes, 921
DNA repair enzyme, 1183
31P, solid state, 1147
Phosphonoamides, cyclic, 1089
Poly(alkylene phosphates), 1171
Purines, from nitroimidazoles, 1661
Ribozymes, 1807
Selenophosphates, 1121
Thiaphosphacyclanes, 1103
Thiophosphates, 1121
Structure Activity Relationship
Sweetness of saccharides, 1569
Theoretical Studies
Cytisine, 1483
b-Lactams, activity of, 1277
Quinoline formation, semiempirical calculation, 965
X-ray Crystal Structures
Aza-crown ethers, 991
Bis(2-aminoethyl)sulfide, Cu(II) complex, 1063
N,N-Bispropyldithiocarbamato bis(triphenylphosphine) Cu(I) complex, 755
Chroman-2-carboxylic acid derivatives, 883
Ethylenediamine-thiocyanato Ni(II) complex, 1067
Hydrazinecarbodithioic acid, derivatives, 1237
1-Phenylimidazole derivatives, 641
Hydrazinecarbodithioic acid esters, 1237
Paracyclophanes, 1351
Piperidineethanols, 1361
Pyrazol-5-ones, Zn(II) complex, 1367
Pyrazole, 1-phenyl, Cu(II) complex, 1381
Schiff bases, 1375
Tetraoxacyclophanes, 1247