Zobrazeno 1 - 10
of 114
pro vyhledávání: '"V. I. Stanko"'
Publikováno v:
Theoretical and Experimental Chemistry. 8:336-339
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be303c2a521a31d8bcc2b79cb803e892
https://doi.org/10.1007/bf00529170
https://doi.org/10.1007/bf00529170
Publikováno v:
Theoretical and Experimental Chemistry. 9:666-670
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50eb398c83453eabbd874b73082bd306
https://doi.org/10.1007/bf00523812
https://doi.org/10.1007/bf00523812
Publikováno v:
Journal of Applied Spectroscopy. 21:1514-1518
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8de39459ac6746aed5ab327e74537dc3
https://doi.org/10.1007/bf00604432
https://doi.org/10.1007/bf00604432
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 30:442-446
1. The data of a detailed x-ray-diffraction study of 1-trimethylsilyl- and trimethyl-germyl-o-carboranes show that the Si-C and Ge-C bonds between the carborane ring and the substituent are larger than the bonds in the substituent itself, and CH3 gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa630d91808de76d34a3eedcbb191b59
https://doi.org/10.1007/bf00949592
https://doi.org/10.1007/bf00949592
Publikováno v:
Journal of Structural Chemistry. 16:573-578
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e4d16608e6f27f3225331e30a47d4ce
https://doi.org/10.1007/bf00754040
https://doi.org/10.1007/bf00754040
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:742-746
We have carried out a complete x-ray structural analysis of (CCH3)2B10H8(CH3)2, one of the products resulting from the methylation of aminated dianions of 1,2-dimethyl-o-carborane, and have shown that the compound with all methyl groups joined to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d16933a78501d1db6344e2e61020f22
https://doi.org/10.1007/bf00925296
https://doi.org/10.1007/bf00925296
Autor:
N. I. Kirillova, M. Yu. Antipin, V. I. Stanko, S. P. Knyazev, Yu. T. Struchkov, V. A. Brattsev
Publikováno v:
Journal of Organometallic Chemistry. 141:133-139
The intramolecular rearrangement involved in the electrophilic methylation of 7,8-B9C2H112− leads after protonation to the methyl derivative of a new isomer of dicarba-nido-undecaborane(13). By an X-ray structure analysis the latter compound is sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5470e02508bd675f668510e99980177
https://doi.org/10.1016/s0022-328x(00)92266-6
https://doi.org/10.1016/s0022-328x(00)92266-6
Autor:
A. M. Alymov, T. A. Babushkina, V. A. Brattsev, S. P. Knyazev, V. I. Stanko, T.P. Klimova, A.M. Vassilyev
Publikováno v:
Journal of Organometallic Chemistry. 78:313-322
The behaviour of the dianions from o-, m- and p-carboranes and of their C-methyl derivatives was studied by means of 11B NMR spectroscopy. The specificity of carborane “redox” isomerization through the dianions is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c734d602a4ce9210fa9659fe21864880
https://doi.org/10.1016/s0022-328x(00)80481-7
https://doi.org/10.1016/s0022-328x(00)80481-7
Publikováno v:
Russian Chemical Reviews. 44:643-669
The structures, methods of synthesis, and chemical properties of closo- and nido-carboranes are discussed and certain general features of the chemical reactions of carboranes are indicated. The bibliography includes 228 references.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6afefa74524b236e69ce30e0c88b9bb8
https://doi.org/10.1070/rc1975v044n08abeh002367
https://doi.org/10.1070/rc1975v044n08abeh002367
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 28:2296-2301
By a complete x-ray diffraction examination of 1-tert-butyl-o-carborane (I) and 1-trimethylsilyl-2-methyl-o-carborane (II), it was found that the bonds between the substituants and the icosahedral skeleton are elongated. The tert-butyl substituent in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72468abf46f8d2ca1fccc819f26614b9
https://doi.org/10.1007/bf00951702
https://doi.org/10.1007/bf00951702