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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and coordination properties of 1-tert-butylchlorophosphino- and 1,2-bis(tert-butylchlorophosphino)-1,2-dicarba-closo-dodecaborane(12) - molecular structures of rac- and meso-1,2-((PBuCl)-Bu-t)(2)C2B10H10 and (R,R,R,R/S,S,S,S)-[{Cu{1,2-((PBu
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Synthesis and coordination properties of 1-tert-butylchlorophosphino- and 1,2-bis(tert-butylchlorophosphino)-1,2-dicarba-closo-dodecaborane(12) - molecular structures of rac- and meso-1,2-((PBuCl)-Bu-t)(2)C2B10H10 and (R,R,R,R/S,S,S,S)-[{Cu{1,2-((PBu

机译:1-叔丁基氯膦基和1,2-双(叔丁基氯膦基)-1,2-二氨基甲酰氯十二烷基硼烷的合成和配位性质(12)-rac-和meso-1,2-(( PBuCl)-Bu-t)(2)C2B10H10和(R,R,R,R / S,S,S,S)-[{Cu {1,2-((PBu

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1-tert-Butylchlorophosphino-1,2-dicarba-closo-dodecaborane(12) (1) and a mixture of stereoisomers of rac- and meso-1,2-bis(tert-butylchlorophosphino)- 1,2-dicarba-closo-dodecaborane(12) (2a, b; 2a:2b = I -. 1) are readily obtained from (BuPCl2)-Bu-t and 1-lithio- and 1,2-dilithio-1,2-dicarba-closo-dodecaborane(12), respectively. The stereoisomers of 2a, b were separated by column chromatography. Compounds I and 2a, b react with [AuCl(tht)] (tht = tetrahydrothiophene) to yield [AuCl(1-(PBuClC2B10H11)-Bu-t)] (3) and [AuCl{1,2-((PBuCl)-Bu-t)(2)C2B10H10}] (4). A mixture of 2a and 2b reacts with CuCl in THF to give (R,R,R,R/S,S,S,S)-[{Cu{1,2-((PBuCl)-Bu-t)(2)C2B10H10} (mu -Cl)}(2)] (5) in 48% yield. Compounds 1-5 were characterised spectroscopically (H-1, P-31, B-11, C-13 NMR; IR), and X-ray structure determinations were carried out on 2a, b and 5. (C) 2001 Published by Elsevier Science Ltd. [References: 57]
机译:1-叔丁基氯膦基1,2-二氨基-叔十二硼烷(12)(1)和rac-和内消旋-1,2-双(叔丁基氯膦基)-1,2-二氨基甲酰氯的立体异构体的混合物-dodecaborane(12)(2a,b; 2a:2b = I..1)很容易从(BuPCl2)-Bu-t和1-lithio-和1,2-diilithio-1,2-dicarba-closo-十二硼烷(12)。通过柱色谱分离2a,b的立体异构体。化合物I和2a,b与[AuCl(tht)](tht =四氢噻吩)反应生成[AuCl(1-(PBuClC2B10H11)-Bu-t)](3)和[AuCl {1,2-((PBuCl)) -Bu-t)(2)C2B10H10}](4)。 2a和2b的混合物与CuCl在THF中反应得到(R,R,R,R / S,S,S,S)-[{Cu {1,2-(((PBuCl)-Bu-t)(2 )C 2 B 10 H 10}(μ-Cl)}(2)](5),收率48%。用光谱表征化合物1-5(H-1,P-31,B-11,C-13 NMR; IR),并在2a,b和5上进行X射线结构测定。(C)2001爱思唯尔科学有限公司[参考号:57]

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