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

Lappaconitine–cyclodextrine 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