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1,2-Dihalodigermenes bearing bulky Eind groups: synthesis, characterization, and conversion to halogermylenoids†
Dalton Transactions ( IF 3.5 ) Pub Date : 2017-12-08 00:00:00 , DOI: 10.1039/c7dt03819d
Naoki Hayakawa 1, 2, 3, 4, 5 , Tomohiro Sugahara 5, 6, 7, 8 , Yasuyuki Numata 1, 2, 3, 4, 5 , Hotaka Kawaai 1, 2, 3, 4, 5 , Kenta Yamatani 1, 2, 3, 4, 5 , Shogo Nishimura 1, 2, 3, 4, 5 , Shun Goda 1, 2, 3, 4, 5 , Yuko Suzuki 5, 6, 7, 8 , Tomoharu Tanikawa 1, 2, 3, 4, 5 , Hidetaka Nakai 1, 2, 3, 4, 5 , Daisuke Hashizume 5, 9, 10, 11 , Takahiro Sasamori 5, 6, 7, 8, 12 , Norihiro Tokitoh 5, 6, 7, 8 , Tsukasa Matsuo 1, 2, 3, 4, 5
Affiliation  

1,2-Dihalodigermenes, (E)-(Eind)XGe[double bond, length as m-dash]GeX(Eind) (X = Br and Cl), bearing the fused-ring bulky Eind group (Eind = 1,1,3,3,5,5,7,7-octaethyl-s-hydrindacen-4-yl) have been isolated as orange-yellow crystals by the ligand redistribution reaction between the diarylgermylene, (Eind)2Ge:, and GeX2·dioxane in toluene via the cleavage and recombination of the Ge–C and Ge–X bonds. The dihalodigermenes have a Ge[double bond, length as m-dash]Ge double bond character in the crystalline state, but dissociate into halogermylenes, (Eind)XGe:, in solution. The addition of excess LiBr to the THF solution of the bromogermylene, (Eind)BrGe:, led to the formation of an equilibrium mixture containing the lithium bromogermylenoid, [Li+][(Eind)GeBr2]. The bromogermylenoid can be isolated as a cryptand-separated potassium ion pair, [K+(crypt-222)][(Eind)GeBr2], which has been structurally characterized.

中文翻译:

1,2-Dihalodigermenes带有庞大的Eind基团:合成,表征和转化为卤代木烯类

1,2-Dihalodigermenes,(E)-(Eind)XGe [双键,长度为m-破折号]GeX(Eind)(X = Br和Cl),带有稠环稠密的Eind基团(Eind = 1,1,3,3,5,5,5,7 ,7- octaethyl-小号-hydrindacen -4-基)已经被diarylgermylene,(EIND)之间的配体再分配反应分离,为橙黄色晶体2的Ge :,和GEX 2 ·二恶烷在甲苯中通过切割和重组Ge–C和Ge–X键。二卤二[双键,长度为m-破折号]锗烯在晶体状态下具有Ge Ge双键特征,但在溶液中解离成卤化亚甲基(Eind)XGe:。将过量的溴化锂添加到溴化亚甲基四氢呋喃(Eind)BrGe:的THF溶液中,导致形成了含有溴化锗烯类锂的平衡混合物[Li+ ] [(Eind)GeBr 2 ] -。可以将溴麦芽孢烯类化合物分离为隐窝分离的钾离子对[K +(crypt-222)] [(Eind)GeBr 2 ] -
更新日期:2017-12-08
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