Journal of Organometallic Chemistry p. 1 - 8 (1997)
Update date:2022-08-02
Topics:
Sato, Masaru
Sensui, Masa-Aki
Bis- and tetrakis(triphenylstannyl)tetrathiafulvalenes were prepared from the corresponding lithio-derivatives and chlorotriphenyltin, and their structures were determined by X-ray analysis. Their absorption maxima in the electronic spectrum showed a bathochromic shift. Their redox potentials shifted only a little to a lower region. The charge-transfer complex of the tetra-substituted derivative with TCNQ was isolated. Bis(trimethylstannyl)tetrathiafulvalene did not react with (η-Cp)(CO)2FeI and the reaction with (COD)PtCl2, followed by addition of tributylphosphine, gave a complex mixture, from which (C2H2S2)Pt(PBu3)2 was isolated in a low yield. The structure was confirmed by X-ray diffraction. A convenient preparation of tetrathiafulvalene and tetraiodotetrathiafulvalene is also reported.
View MoreContact:+36(21)2523420
Address:Head office: 1102 Budapest, SZENT LASZLO TER 24/B. 1/1., HUNGARY / CHINA
Contact:+86-20-32051076
Address:1105,Building A, International Business Incubator,Science City
Beijing Apis Biotechnology Co., Ltd.
Contact:86-010-67856775-8551
Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Suzhou Chiral Pharmaceuticals Co., Ltd.
Contact:86-0512-63197058
Address:Building A, No. 2358, Chang'an Road, Wujiang Science Park
SHANGHAI T&W PHARMACEUTICAL CO., LTD.
website:http://www.trustwe.com
Contact:+86-21-61551611
Address:601, No. 1, 2277 Nong, Zu Chongzhi Road, Zhangjiang Hightech. Park, Pudong
Doi:10.1016/S0040-4039(97)01182-9
(1997)Doi:10.1055/s-0040-1707223
(2020)Doi:10.1515/znb-1997-0615
(1997)Doi:10.1021/jm970283e
(1997)Doi:10.1016/S0960-894X(98)00670-2
(1998)Doi:10.1021/ja026654k
(2003)