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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Activation of Molecular Hydrogen by Bis((5),(1)-pentafulvene)-titanium Complexes - Efficient Formation of Titanium(III)hydrides
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Activation of Molecular Hydrogen by Bis((5),(1)-pentafulvene)-titanium Complexes - Efficient Formation of Titanium(III)hydrides

机译:通过双((5),(1) - (1)-PentafulVene) - 钛(III)氢化物的高效形成 - 氢化物的分子氢气活化

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摘要

The synthesis and crystal structures of two dinuclear titanocene hydride complexes are reported. Both complexes, namely bis((5)-(di-para-tolylmethyl)cyclopentadienyl)titanium hydride dimer, [((5)-C20H19)(2)Ti(-H)](2) (2a), and bis((5)-2-adamantylcyclopentadienyl)-titanium hydride dimer, [((5)-C15H19)(2)Ti(-H)](2) (2b), are formed via activation of molecular hydrogen by the corresponding bis((5),(1)-pentafulvene)titanium complexes 1a and 1b at ambient temperatures and pressures in high yields. The hydride complexes 2a and 2b exhibit planar [Ti2H2] cores and, as a result of the heterolytic cleavage of molecular hydrogen, substituted Cp Ligands were formed during the reaction.
机译:报道了两种二核二碳烯氢化物配合物的合成和晶体结构。 复合物,即双((5) - (二 - 甲苯甲基)环戊二烯基)氢化物二聚体,[((5)-C20H19)(2)Ti(2)(2A)和BIS( (5)-2-金刚氨酰环戊二烯基) - 氢化物二聚体,[((5)-C15H19)(2)Ti(2)Ti(2)(2)(2b)通过相应的双(( 5),(1) - (1) - 富氟戊烷)钛配合物1a和1b在环境温度和高收率的压力下。 氢化物配合物2a和2b表现出平面[ti2h2]核心,并且由于分子氢的异解裂解,在反应过程中形成取代的Cp配体。

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