Reaction of elemental antimony with sulfur under mild hydrothermal conditions yielded different polysulfidoclusters of antimony. These were isolated as tetraphenylphosphonium salts [P(C 6 H 5 ) 4 ] 3 Sb 3 S 25 and [P(C 6 H 5 ) 4 ] 2 Sb 2 S 15 2(C 3 N 2 H 6 ) and their crystal structures were determi
Synthesis and crystal structure of silver and argentate complexes of mixed halocarborane anions, (C5H5N)2Ag(1-HCB11Br5I6)(C5H5N) and [{(CH3CN)4Ag3}{Ag(CB11I5Br6)2}]n
β Scribed by Chi-Wing Tsang; Qingchuan Yang; Thomas C. W. Mak; Zuowei Xie
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 217 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0268-2605
- DOI
- 10.1002/aoc.455
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β¦ Synopsis
Abstract
The first argentate salt of carborane anion, [{(CH~3~CN)~4~Ag~3~}{Ag(CB~11~I~5~Br~6~)~2~}]~n~, was prepared from K~2~[CB~11~I~5~Br~6~] and AgNO~3~ followed by recrystallization from acetonitrile. Singleβcrystal Xβray analyses indicate that the CB~11~I~5~Br~6~^2β^ dianion has a significantly different coordination motif from that of the CB~11~Br~5~I~6~^β^ monoanion. This result suggests that the polarity of the CB~11~ cage can be changed after deprotonation of the cage Cο£ΏH proton. Copyright Β© 2003 John Wiley & Sons, Ltd.
π SIMILAR VOLUMES
Synthesis and crystal structure of 1,6-Bis-(N,Ndiethylaminothiocarbamoylimino)-1,6-diphenyl-2,5-dithiahexane are reported as well as those of its dimeric Ag I complex (as monotoluene adduct of the diperchlorate) and its tetrameric l-tetrabromo Ag I complex.
Treating [Cp\*V(l-Cl) 2 ] 3 (Cp\* = C 5 Me 5 ) and [(2,6-i-Pr 2 C 6 H 3 N) 2 MoMe 2 ], respectively, with Me 3 SnF afforded the title compounds [Cp\*V(l-F) 2 ] 4 (1) and [(2,6-i-Pr 2 C 6 H 3 N) 2 MoF 2 ] Β΄THF ( 2). 1 has a tetrameric structure, in which four V atoms can be regarded as being arranged