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1.
K. A. Frolov V. V. Dotsenko S. G. Krivokolysko A. N. Chernega V. P. Litvinov 《Russian Chemical Bulletin》2005,54(5):1340-1342
Reduction of (E)-3-aryl-2-(4-arylthiazol-2-yl)acrylonitriles with lithium aluminum hydride in dry ether afforded (Z)-1-amino-3-aryl-2-(thiazol-2-yl)prop-1-ene derivatives in 15 to 40% yields. The structure of (Z)-1-amino-3-(2-chlorophenyl)-2-[4-(4-methylphenyl)thiazol-2-yl]prop-1-ene was confirmed by X-ray diffraction analysis.
Dedicated to Academician N. K. Kochetkov on the occasion of his 90th birthday.
__________
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1301–1303, May, 2005. 相似文献
2.
Three Pd(II) complexes [Pd2(μ-Cl)2{7,8-(PPh2)2-7,8-C2B9H10}2] · 0.25CH2Cl2 (1), [Pd{7,8-(PPh2)2-7,8-C2B9H10}2] · 4CHCl3 (2) and [PdCl2(1,2-(PPh2)2-1,2-C2B10H10)] (3) have been synthesized by the reactions of 1,2-(PPh2)2-1,2-C2B10H10 with PdCl2 in acetonitrile, cyanophenyl and dichloromethane, respectively. A fourth complex, [PdI2(1,2-(PPh2)2-1,2-C2B10H10)] (4), was obtained by a ligand exchange reaction through the substitution of the Cl− of complex 3 with I−. All four complexes have been characterized by elemental analysis, FT-IR, 1H and 13C NMR spectroscopy and X-ray structure determination. Single crystal X-ray determination showed that the carborane cage, nido for 1, 2 and closo for 3, 4, was coordinated bidentately to the Pd atom through the two P atoms, and the geometry at the Pd atom was square-planar in all the complexes. 相似文献
3.
1H and13C NMR spectra of 7-diethylamino-4-(1,2,3-triazol-1-yl)-2H-1-benzopyran-2-one derivatives have been studied. The location of the substituent in the 1,2,3-triazole ring was determined by the 2D COLOC method. It was established that the H(3) and H(5) protons in the coumarin moiety experience anisotropic influence of the phenyl subsituent at the C(5) atom in the triazole ring.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1330–1332, July, 1994. 相似文献
4.
V. B. Kobychev N. M. Vitkovskaya E. Yu. Larionova N. S. Klyba B. A. Trofimov 《Russian Chemical Bulletin》2000,49(3):408-414
Ab initio study of the pathways of migration of the double bond in the 3-methylthioprop-1-ene (1) and 3-methoxyprop-1-ene (2) molecules with participation of hydroxide ion was carried out by the RHF/6-31+G* and MP2/6-31+G//RHF/6-31+G* methods. Conformational isomerism of the initial molecules and reaction products was considered. The distinctions are discussed
in the spatial and electronic structure of intermediate carbanions stabilized (for1) due to the negative hyperconjugation. Stationary points corresponding to complexes between the molecules under study and
the hydroxide ion and between the corresponding carbanion and water molecule were localized on the potential energy surfaces
of the proton transfer reactions. For2, the single-stage mechanism of prototropic rearrangement involving the H atom of the hydroxide ions was found to be more
energetically preferable than the two-stage mechanism, whereas both mechanisms are expected to be equiprobable for1.
For Parts 1–3, see Refs. 1–3.
Translated fromIzvestiya Akademii Nauk. Seriya Kimicheskaya, No. 3, pp. 407–413, March, 2000. 相似文献
5.
Tushar S. Basu Baul Wandondor Rynjah Monique Biesemans Michal Holèapek Anthony Linden 《Journal of organometallic chemistry》2004,689(25):4691-4701
A series of dibutylbis{5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoato}tin(IV) complexes, Bu2Sn(LH)2, have been prepared and characterized by 1H, 13C, 119Sn NMR and ESI mass spectrometry in solution. The structures of the complexes Bu2Sn(L1H)2 (1), Bu2Sn(L3H)2 (3), Bu2Sn(L4H)2 (4), and Bu2Sn(L6H)2 (6) (L = 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoate: aryl = phenyl (L1H), 3-methylphenyl (L3H), 4-methylphenyl (L4H) and 4-bromophenyl (L6H)) were determined by X-ray crystallography and 117Sn CP-MAS NMR spectroscopy in the solid state. In general, the complexes were found to adopt a skew-trapezoidal bipyramidal arrangement around the tin atom. In addition, there are weak bridging intermolecular Sn?O contacts in complexes 1 and 3, but not in 4 and 6, where one of the hydroxy oxygen atoms from a neighboring molecule coordinates weakly with the Sn atom, thereby completing a seventh coordination site in the extended Sn coordination sphere. The Sn?O distance is 3.080(2) and 3.439(2) Å in 1 and 3, respectively, which are significantly shorter than the sum of the van der Waals radii of the Sn and O atoms (∼3.8 Å). In 1, this Sn?O interaction links the molecules into polymeric chains. In 3, these interactions link pairs of molecules into head-to-head dimeric units. The in vitro cytotoxicity of compound 2 indicates better results than cisplatin and etoposide against seven well characterized human tumor cell lines. 相似文献
6.
Qibo Liu 《Journal of fluorine chemistry》2009,130(10):922-925
(E)-(1,2-Difluoro-1,2-ethenediyl)bis[tributylstannane], 3, readily undergoes a Pd(PPh3)4/CuI-catalyzed cross-coupling reaction with iodotrifluoroethene to yield (E)-octafluoro-1,3,5-hexatriene, 4, in high isomeric purity. (1Z,3E,5Z)-(1,2,3,4,5,6-Hexafluoro-1,3,5-hexenetriyl)bis[tributylstannane], 7, was sequentially prepared from (1Z,3E,5Z)-(1,2,3,4,5,6-hexafluoro-1,3,5-hexenetriyl)bis[triethylsilane], 5, which was prepared via a Pd(PPh3)4/CuI-catalyzed cross-coupling reaction of 3 with (E)-1,2-difluoro-1-iodo-2-triethylsilylethene, 6. Pd(PPh3)4/CuI cross-coupling of 7 with iodotrifluoroethene gave (3E,5E,7E)-dodecafluoro-1,3,5,7,9-decapentaene, 8. 相似文献
7.
Tushar S. Basu Baul Cheerfulman Masharing Monique Biesemans Robert Jirásko 《Journal of organometallic chemistry》2005,690(12):3080-3094
The diorganotin(IV) compounds, [Me2SnL2(OH2)]2 (1), [nBu2SnL2(OH2)]2 (2), [nBu2SnL1]3 · 0.5C3H6O (3), [nBu2SnL3]3 · 0.5C6H6 (4) and [Ph2SnL3]n · 0.5C6H6 (5) (L = carboxylic acid residue, i.e., 2-{[(E)-1-(2-oxyaryl)alkylidene]amino}acetate), were synthesized by treating the appropriate diorganotin(IV) dichloride with the potassium salt of the ligand in anhydrous methanol.The reaction of Ph2SnL2 (L = 2-{[(E)-1-(2-oxyphenyl)ethylidene]amino}acetate) with 1,10-phenanthroline (Phen) yielded a 1:1 adduct of composition, [Ph2SnL2(Phen)] (6).The crystal structures of 1-6 were determined.The crystal of 1 is composed of centrosymmetric dimers of the basic Me2SnL2(OH2) moiety, where the two Sn-centres are linked by two asymmetric Sn-O?Sn bridges involving the carboxylic acid O atom of the ligand and a long Sn?O distance of 3.174(2) Å.The dimers are further linked into columns by hydrogen bonds.The coordination geometry about the Sn atom is a distorted pentagonal bipyramid with the two methyl groups in axial positions.The structure of 2 is similar.The same Sn atom coordination geometry is observed in compound 3, which is a cyclic trinuclear[nBu2SnL1]3 compound. Each Sn atom is coordinated by the phenoxide O atom, one carboxylate O atom and the imino N atom from one ligand and both the exo- and endo-carboxylate O atoms (mean Sn-O(exo): 2.35 Å; Sn-O(endo): 2.96 Å) from an adjacent ligand to form the equatorial plane, while the two butyl groups occupy axial positions. Compound 4 was found to crystallize in two polymorphic forms. The Sn-complex in both forms has a trinuclear [nBu2SnL3]3 structural motif similar to that found in 3. In compound 5, distorted trigonal bipyramidal Ph2SnL3 units are linked into polymeric cis-bridged chains by a weak Sn?O interaction (3.491(2) Å) involving the exocyclic O atom of the tridentate ligand of a neighboring Sn-complex unit. This interaction completes a highly distorted octahedron about the Sn atom, where the weakly coordinated exocyclic O atom and one phenyl group are trans to one another. In contrast, a monomeric distorted pentagonal bipyramidal geometry is found for adduct 6 where the Sn-phenyl groups occupy the axial positions. The solution and solid-state structures are compared by using 119Sn NMR chemical shift data. Compounds 1-6 were also studied using ESI-MS and their positive- and negative-ions mass fragmentation patterns are discussed. 相似文献
8.
应用芳基异氰酸酯与烯基膦亚胺1的氮杂Wittig反应, 得到的碳二亚胺2, 再与水合肼作用得到氨基咪唑啉酮衍生物4. 而后用4与芳基异氰酸酯(或酰氯)、三苯基膦、六氯乙烷和三乙胺“一锅”反应, 得到4,5-二氢咪唑并[1,2-b]-1',2',4'-三唑-4-酮衍生物6或7. 探讨了所合成新型稠杂环化合物的生物活性, 结果表明部分化合物表现出良好的杀菌活性. 如7c在50 mg/L浓度时, 对棉花枯萎菌、稻瘟菌、黄瓜灰霉菌和油菜菌核菌的抑制率均达100%. 相似文献
9.
Shin-ichi Takekuma Masanori Hirosawa Masato Sasaki Hideko Takekuma 《Tetrahedron》2006,62(15):3732-3738
Reactions of the title ethylene derivatives, (E)-1,2-di(3-guaiazulenyl)ethylene (1) and 2-(3-guaiazulenyl)-1,1-bis(4-methoxyphenyl)ethylene (2), with a 2 M amount of TCNE in benzene at 25 °C for 24 h under argon give new cycloaddition compounds, 1,1,2,2,11,11,12,12-octacyano-3-(3-guaiazulenyl)-8-isopropyl-5,10-dimethyl-1,2,3,6,9,10a-hexahydro-6,9-ethanobenz[a]azulene (3) from 1 and 1,1,2,2,11,11,12,12-octacyano-8-isopropyl-3,3-bis(4-methoxyphenyl)-5,10-dimethyl-1,2,3,6,9,10a-hexahydro-6,9-ethanobenz[a]-azulene (4) from 2, respectively, in 66 and 87% isolated yields. Comparative studies on the above reactions as well as the spectroscopic properties of the unique products 3 and 4, possessing interesting molecular structures, are reported and, further, a plausible reaction pathway for the formation of these products is described. 相似文献
10.
Tushar S. Basu Baul Archana Mizar Eleonora Rivarola Michal Hol?apek Ulli Englert 《Journal of organometallic chemistry》2006,691(16):3416-3425
A series of cis-bis{5-[(E)-2-(aryl)-1-diazenyl]quinolinolato}diphenyltin(IV) complexes have been synthesized and characterized by 1H, 13C, 119Sn NMR, ESI-MS, IR and 119mSn Mössbauer spectroscopic techniques in combination with elemental analysis. The structures of a ligand L6H (i.e., 5-[(E)-2-(4-ethoxyphenyl)-1-diazenyl]quinolin-8-ol) and three diphenyltin(IV) complexes, viz., Ph2Sn(L1)2 · (CH3)2CO (1), Ph2Sn(L4)2 (4) and Ph2Sn(L5)2 (5) (L = 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-ol: aryl = phenyl - (L1H); 4′-methylphenyl - (L4H) and 4′-bromophenyl - (L5H)) were determined by single crystal X-ray diffraction. In general, the complexes were found to adopt a distorted cis-octahedral arrangement around the tin atom. These complexes retain their solid-state structure in non-coordinating solvent as evidenced by 119Sn NMR spectroscopic results. The in vitro cytotoxicity of 1 is reported and compared with Ph2Sn(Ox)2 (Ox = deprotonated quinolin-8-ol) against seven well characterized human tumor cell lines. 相似文献
11.
(R)-4-Menthenone in the synthesis of optically pure sex pheromone of the peach leafminer moth (Lyonetia clerkella) 总被引:1,自引:0,他引:1
Kharisov R. Ya. Latypova E. R. Talipov R. F. Muslukhov R. R. Ishmuratov G. Yu. Tolstikov G. A. 《Russian Chemical Bulletin》2003,52(10):2267-2269
The synthesis of (14S)-methyloctadec-1-ene, sex pheromone of the peach leafminer moth (Lyonetia clerkella), is described to demonstrate a new potential of the synthetic use of (R)-4-menthenone. 相似文献
12.
A simple and effective procedure for the enantioselective synthesis of (R)- and (S)-moprolol was described. The key step was the asymmetric synthesis of enantiopure (R)- and (S)-guaifenesin, which were synthesized from enantioenriched (R)-3-chloro-l,2-propanediol and (S)-epichlorohydrin via kinetics of hydrolysis resolution of racemic epichlorohydrin by chiral Salen-Co^Ⅲ complex. The e.e. values of both the optical compounds were above 98%, and the chemical structures of the target compounds were confirmed by ^1H NMR, ^13C NMR, IR, and MS. 相似文献
13.
Hans-Georg Henning Le Hoang Thanh Jörg Laue Barbara Urban Günter Reck 《Monatshefte für Chemie / Chemical Monthly》1994,125(1):95-105
Summary The enamine-type methylene-N-heterocycles1–5 react with cyclic 2-ethoxymethylene-1,3-dicarbonyl compounds6 to give 2-[2-(hetarylidene)ethylidene]-1,3-dicarbonyl compounds7–14. The result of the reactions between 1,2-dihydro-1-methyl-2-methylene-quinoline (1a) and cyclic 1,3-dicarbonyl compounds depends on the nature of the dihydro intermediatesA/B. Dehydrogenation of keton intermediatesA results in 2-(1,2-dimethyl-4(1H)-quinolylidene)-1,3-dicarbonyl compounds17–21. Enol intermediatesB with 6-membered dicarbonyl ring form 6,12-methano-dibenz-[d,g][1,3]oxazocinones22–25.1H NMR spectra and X-ray structure analysis prove the structure of23.
Reaktionen cyclischer 1,3-Dicarbonylverbindungen mit 1,2(1,4)-Dihydro-1-methyl-2(4)-methylen-N-heterocyclen. Ein neuer Zugang zu 6,12-Methano- dibenz[d,g][1,3]oxazocinonen
Zusammenfassung Aufgrund ihres Enamincharakters reagieren die Methylen-N-heterocyclen1–5 mit cyclischen 2-Ethoxymethylen-1,3-dicarbonylverbindungen6 zu den 2-[2-(Hetaryliden)ethyliden]-1,3-dicarbonylverbindungen7–14. Das Ergebnis der Reaktionen zwischen 1,2-Dihydro-1-methyl-2-methylen-chinolin (1a) und cyclischen 1,3-Dicarbonylverbindungen hängt von der Natur der zwischenzeitlich entstehenden DihydroverbindungenA/B ab. Die Intermediat-KetoneA gehen durch Dehydrierung während der Reaktion in die 2-(1,2-Dimethyl-4(1H)chinolyliden)-1,3-dicarbonylverbindungen17–21 über. Die Intermediat-EnoleB mit sechsgliedrigem Dicarbonylring bilden in intramolekularer Reaktion die 6,12-Methano-dibenz[d,g][1,3]oxazocinone22–25, deren Struktur am Beispiel der Verbindung23 durch1H-NMR sowie durch Röntgenkristallstrukturanalyse bewiesen wird.相似文献
14.
Tushar S. Basu Baul Archana Mizar Giuseppe Ruisi Monique Biesemans 《Journal of organometallic chemistry》2009,694(14):2142-4247
Reactions of nBu2SnCl(L1) (1), where L1 = acid residue of 5-[(E)-2-(4-methoxyphenyl)-1-diazenyl]quinolin-8-ol, with various substituted benzoic acids in refluxing toluene, in the presence of triethylamine, yielded dimeric mixed ligand di-n-butyltin(IV) complexes of composition [nBu2Sn(L1)(L2-6)]2 where L2 = benzene carboxylate (2), L3 = 2-[(E)-2-(2-hydroxy-5-methylphenyl)-1-diazenyl]benzoate (3), L4 = 5-[(E)-2-(4-methylphenyl)-1-diazenyl]-2-hydroxybenzoate (4), L5 = 2-{(E)-4-hydroxy-3-[(E)-4-chlorophenyliminomethyl]-phenyldiazenyl}benzoate (5) and L6 = 2-[(E)-(3-formyl-4-hydroxyphenyl)-diazenyl]benzoate (6). All complexes (1-6) have been characterized by elemental analyses, IR, 1H, 13C and 117Sn NMR and 119Sn Mössbauer spectroscopy and their structures were determined by X-ray crystallography, complemented by 117Sn CP-MAS NMR spectroscopy studies in the solid state. The crystal structure of 1 reveals a distorted trigonal bipyramidal coordination geometry around the Sn-atom where the Cl- and N-atoms of ligand L1 occupy the axial positions. In complexes 2-5, the molecules are centrosymmetric dimers in which the Sn-atoms are connected by asymmetric μ-O bridges through the quinoline O-atom to give an Sn2O2 core. The differences in the Sn-O bond lengths within the bridge range from 0.28 to 0.48 Å, with the longer of the Sn-O distances being in the range 2.56-2.68 Å and the most symmetrical bridge being in 5. The carboxylate group is almost symmetrically bidentate coordinated to the tin atom in 5 (Sn-O distances of 2.327(2) and 2.441(2) Å), unlike the other complexes in which the distance of the carboxylate carbonyl O-atom from the tin atom is in the range 2.92-3.03 Å. The structure of 5 displays a more regular pentagonal bipyramidal coordination geometry about each tin atom than in 2-4. In contrast, the centrosymmetric dimeric structure of 6 involves asymmetric carboxylate bridges, resulting in a different Sn2C2O4 motif. The Sn-O bond lengths in the bridge differ by about 0.6 Å, with the longer distance involving the carboxylate carbonyl O-atom (2.683(2) and 2.798(2) Å for two molecules in the asymmetric unit). The carboxylate carbonyl O-atom has a second, even longer intramolecular contact to the Sn-atom to which the carboxylate group is primarily coordinated, with these Sn?O distances being as high as 3.085(2) and 2.898(2) Å. If the secondary interactions are considered, all the di-n-butyltin(IV) complexes (2-6) display a distorted pentagonal bipyramidal arrangement about each tin atom in which the n-butyl groups occupy the axial positions. 相似文献
15.
Tushar S. Basu Baul Archana Mizar George Eng Michal Hol?apek Monique Biesemans Ray Butcher 《Journal of organometallic chemistry》2006,691(12):2605-2613
A series of cis-bis{5-[(E)-2-(aryl)-1-diazenyl]quinolinolato}dibenzyltin(IV) complexes have been synthesized by reacting sodium salts of 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-ol (LH) and dibenzyltin dichloride. These complexes have been characterized by 1H, 13C, 119Sn NMR, ESI-MS in solution and by IR and 119mSn Mössbauer, 117Sn CP-MAS NMR spectroscopy in solid state. In addition, the structures of three of the dibenzyltin(IV) complexes, viz., Bz2Sn(L2)2 (2), Bz2Sn(L3)2 (3), and Bz2Sn(L5)2 (5) (L = 5-[(E)-2-(aryl)-1-diazenyl]quinolin-8-ol: aryl = 4′-methylphenyl- (L2H), 4′-methoxylphenyl- (L3H) and 4′-bromophenyl- (L5H)) were determined by single-crystal X-ray diffraction. In general, the complexes were found to adopt a distorted cis-octahedral arrangement around the tin atom in both solution and solid state. 相似文献
16.
Shkumbatiuk R Bazel YR Andruch V Török M 《Analytical and bioanalytical chemistry》2005,382(6):1431-1437
A new, simple, rapid, and sensitive spectrophotometric method has been developed for the determination of nitrophenols [picric acid (PA); dinitrophenols (DNP)] in wastewater samples. The method is based on the reaction of nitrophenols with 2-[(E)-2-(4-diethylaminophenyl)-1-ethenyl]-1,3,3-trimethyl-3 H-indolium chloride reagent to form the colored ion associates, which are extracted by organic solvents. The molar absorptivity of the ion associates of PA with the investigated reagent ranges from 8.3×104 to 11.3×104 L mol–1 cm–1, depending on the extractant. Because only PA is extracted in an acidic medium with the investigated reagent, but both PA and DNP are extracted in an alkaline medium, it is possible to determine both substances in a mixture. Appropriate reaction conditions have been established. The absorbance of the colored extracts obeys Beers law in the range of 0.04–4.58 mg L–1 PA, 1.0–18.4 mg L–1 2,4-DNP and 1.2–14.7 mg L–1 2,6-DNP, respectively. The limit of detections, calculated from a blank test (n=10; P=0.95), are 0.05 mg L–1 PA, 0.9 mg L–1 (2,4-DNP), and 1.1 mg L–1 (2,6-DNP), respectively. 相似文献
17.
Dmitrenok A. S. Radhika P. Anjaneyulu V. Subrahmanyam C. Subba Rao P. V. Dmitrenok P. S. Boguslavsky V. M. 《Russian Chemical Bulletin》2003,52(8):1868-1872
Sphingolipids and glycolipids including previously unknown (2S,3S,4R)-1,3,4-trihydroxy-2-(2-(R)-hydroxyoctadecanoylamino)octadec-8E-ene, (2S,3R)-1,3-dihydroxy-2-octadecanoylamino-4E,8E-hexadecadiene, and (2-hydroxy-3-hexadecyloxypropyl)--L-fucopyranoside were isolated from soft corals collected on the shelf near the Andaman Islands (Indian Ocean). The structures of all compounds were established by spectroscopic methods and chemical analyses. The lipids possessed antibacterial activity against Bacillus subtilis, Bacillus pumilus, Escherichia coli, and Pseudomonas aeruginosa and antifungal activity against Aspergillus niger, Rhizopus oryzae, and Candida albicans. 相似文献
18.
Belokon" Yu. N. Maleev V. I. Savel"eva T. F. Ikonnikov N. S. 《Russian Chemical Bulletin》2001,50(6):1037-1040
Both enantiomers of -methylserine were synthesized with the use of NiII complexes based on the chiral recyclable reagent (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide. Intermediate diastereomeric complexes were separated by crystallization of their O-acetyl derivatives. 相似文献
19.
G. Yu. Ishmuratov R. Ya. Kharisov O. V. Botsman V. V. Zorin G. A. Tolstikov 《Russian Chemical Bulletin》2000,49(11):1899-1901
Effective routes for the synthesis of (S)-2-acetoxytridecane, the sex pheromone of the fruit flyDrosophila mulleri, and (S)-1-methylbutyl 2-methyl- and 2,4-dimethylpent-2E-enoates, components of the aggregation pheromone of the lesser grain borerRhyzopertha dominica, were developed on the basis of (S)-4-methylhex-5-en-1-yl tosylate accessible from (S)-(+)-dihydromyreene.
Published inIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1929–1931, November, 2000. 相似文献
20.
Tushar S. Basu Baul Keisham Surjit Singh Robert Jirásko Anthony Linden 《Journal of organometallic chemistry》2005,690(19):4232-4242
The triphenyltin(IV) complexes of 4-[((E)-1-{2-hydroxy-5-[(E)-2-(2-carboxyphenyl)-1-diazenyl]phenyl}methylidene)amino]aryls (aryls = 4-CH3, 4-Br, 4-Cl, 4-OCH3) have been synthesized and characterized by 1H-, 13C-, 119Sn-NMR, ESI mass spectrometry, IR and 119mSn Mössbauer spectroscopic techniques in combination with elemental analysis. The crystal structures of a representative carboxylate ligand (aryl = 4-CH3) and three Sn complexes, viz., polymeric (Ph3Sn[O2CC6H4{NN(C6H3-4-OH(C(H)NC6H4X-4))}-o])n (X = Me (1) and Br (2)) and dimeric (Ph3Sn[O2CC6H4{NN(C6H3-4-OH(C(H)NC6H4X-4))}-o])2 (X = OMe (4)) complexes are reported. The coordination environment in each complex is trigonal bipyramidal trans-Ph3SnO2. A single zwitterionic carboxylate ligand bridges adjacent Sn atoms via the carboxylate and phenoxide O atoms. 相似文献