Copper(II) complexes with ethyl [(Pyrazolo-1-carbothioyl)-amino]acetate derivatives: Synthesis and structure Научная публикация
Журнал |
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
ISSN: 1070-3284 |
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Вых. Данные | Год: 2003, Том: 29, Номер: 6, Страницы: 375-384 Страниц : 10 DOI: 10.1023/A:1024073808779 | ||||
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Реферат:
Optically active derivative of the natural monoterpene (+)-3-carene, namely, ethyl (3bS,4aR)-[(3,4,4-trimethyl-3b,4,4a,5 -tetrahydrocyclopropa [3,4]cyclopenta[1,2-c]pyrazole-1-carbothioyl)-amino]acetate (HLI) and ethyl [(3,5-dimethyl-pyrazole-1-carbothioyl)-amino] acetate (HL2) were synthesized. Paramagnetic complexes 2 [(CuLCl)-Cl-1](n) (I) and [Cu2L22 Cl-2] (II) were prepared. According to X-ray diffraction data, complex I with anion of (+)-3-carene derivative has chain structure, whereas complex II with anion of HL2, which has no carbocyclic fragments, is a pseudodimer. Organic anions act as tetradentate bridging, cyclic ligands forming five-membered CuN3C and CuNOC2 metal cycles. Coordination polyhedron of Cu(ClN2O + S) in complexes I and II is a square pyramid. The values of mu(eff) for complexes I and II (1.88 and 1.84 mu(B), respectively) are constant in the temperature interval 78-300 K, which means that the unpaired electrons of Cu(II) ions do not exhibit any noticeable exchange interactions.
Библиографическая ссылка:
Savel'eva Z.
, Popov S.
, Glinskaya L.
, Klevtsova R.
, Ikorskii V.
, Boguslavskii E.
, Tkachev A.
, Larionov S.
Copper(II) complexes with ethyl [(Pyrazolo-1-carbothioyl)-amino]acetate derivatives: Synthesis and structure
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2003. V.29. N6. P.375-384. DOI: 10.1023/A:1024073808779 WOS Scopus РИНЦ
Copper(II) complexes with ethyl [(Pyrazolo-1-carbothioyl)-amino]acetate derivatives: Synthesis and structure
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2003. V.29. N6. P.375-384. DOI: 10.1023/A:1024073808779 WOS Scopus РИНЦ
Идентификаторы:
Web of science | WOS:000183799300001 |
Scopus | 2-s2.0-1642492680 |
РИНЦ | 31258619 |
OpenAlex | W293824487 |