Zobrazeno 1 - 9
of 9
pro vyhledávání: '"A. S. Gel'fond"'
Autor:
A. Sh. Mukhtarov, B. D. Chernokal'skii, Yu. G. Galyametdinov, A. V. Il'yasov, A. A. Vafina, A. S. Gel'fond, Yu. M. Kargin, B. V. Mel'nikov, I. D. Morozova
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 21:2111-2114
1. The mechanism of the polarographic reduction of nitrophenyldiethylarsines, their oxides and sulfides in aprotonic medium was studied. Schemes of the subsequent chemical reactions after the reception of a second electron by these systems were propo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1b3f5c5778bdd32b5eb825e9bee5bc1
https://doi.org/10.1007/bf00855277
https://doi.org/10.1007/bf00855277
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 18:1381-1384
1. The UV spectra of a number of para-substituted phenyldialkylarsines and their oxides were studied. 2. The diethylarsinyl and diethylarsine groups behave as meta-orienters, in accord with the concept of participation of the d-orbitals of the As ato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2f7e334a1c4f782169acfe635a4f53b
https://doi.org/10.1007/bf00908735
https://doi.org/10.1007/bf00908735
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 19:2341-2345
1. Oxides of triphenyl- and aryldiethylarsines in dimethylformamide are reduced in one irreversible two-electron step. In the presence of phenol, four or more electrons per molecule are consumed for the reduction. 2. The satisfactory correlation of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e4e3484a4b0d3cfc3c76c0810c55de6
https://doi.org/10.1007/bf00859072
https://doi.org/10.1007/bf00859072
Autor:
I. A. Lamanova, A. S. Gel'fond, S. V. Izosimova, B. D. Chernokal'skii, Yu. G. Galyametdinov, R. R. Shagidullin, G. M. Dorozhkina
Publikováno v:
Journal of Applied Spectroscopy. 23:1350-1352
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4de0a9566d9e480c42073ff56aae4542
https://doi.org/10.1007/bf00618083
https://doi.org/10.1007/bf00618083
Autor:
A. S. Gel'fond, A. A. Barlev, B. D. Chernokal'skii, A. V. Il'yasov, A. A. Vafina, Yu. G. Galyametdinov
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 25:672-674
1. Arsinobenzoates are reduced in three steps, the first of which involves one electron and is reversible. The diethylarsinyl groups are electron acceptors. Transfer of a second electron leads to the rupture of the As-C bond and to the formation of m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a22b786424829c5a589b7c5f31d7e7d5
https://doi.org/10.1007/bf01106682
https://doi.org/10.1007/bf01106682
Autor:
B. S. Gel'fond, E. A. Ivanov
Publikováno v:
Radiophysics and Quantum Electronics. 10:380-382
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fe6a85182a1e198906d3df5f7b8be49
https://doi.org/10.1007/bf01039417
https://doi.org/10.1007/bf01039417
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7c0fac415523ff1f89613253c775d2f
https://doi.org/10.1002/chin.197610264
https://doi.org/10.1002/chin.197610264
Autor:
Yu. G. Galyametdinov, R. Kh. Gataullina, B. D. Chernokal'skii, A. S. Gel'fond, V. G. Mironova
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1f830f30b0d492189e3f88db4f4b5a
https://doi.org/10.1002/chin.197307347
https://doi.org/10.1002/chin.197307347
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67dad590f873151dd05d9630fbb0d544
https://doi.org/10.1002/chin.197018338
https://doi.org/10.1002/chin.197018338