...
首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >The nature of aryloxide and arylsulfide ligand bonding in dimethyltitanium complexes containing cyclopentadienyl ligation
【24h】

The nature of aryloxide and arylsulfide ligand bonding in dimethyltitanium complexes containing cyclopentadienyl ligation

机译:含环戊二烯基连接的二甲基钛配合物中芳氧基和芳硫醚配体键的性质

获取原文
获取原文并翻译 | 示例

摘要

A series of dimethyltitanium compounds [CpTi(EAr)Me_2] (E = O,S) ligated by one cyclopentadienyl (Cp) and one aryloxide (OAr) or arylsulfide (SAr) have been structurally characterized in order to gain a better understanding of aryloxide and arylsulfide bonding in these systems.Experimental structures were compared to those predicted by density functional theory (DFT).Bonding in the arylsulfide systems was found to be significantly different from bonding in the aryloxide systems.The aryloxide ligands exhibited wide Ti-O-Ar angles (>150~o) with the Ar group oriented proximal to the Cp group.DFT computations revealed two conformers for the arylsulfide systems.Arylsulfides with the Ar group proximal to the Cp group had a predicted Ti-S-Ar angle of approx 120~° while those with the Ar group distal to the Cp group had a measured and predicted Ti-S-Ar angle of approx 100~°.Molecular and natural bond orbital (NBO) analyses were employed to explain the nature of ligand bonding in these systems.
机译:通过结构表征了一系列由一个环戊二烯基(Cp)和一个芳基氧化物(OAr)或芳基硫醚(SAr)连接的二甲基钛化合物[CpTi(EAr)Me_2](E = O,S),以更好地理解芳基氧化物将实验结构与密度泛函理论(DFT)预测的结构进行了比较,发现芳硫醚体系中的键合与芳氧化物体系中的键合显着不同,芳氧化物配体具有宽的Ti-O-Ar Ar基团朝向Cp基团的角度(> 150°o).DFT计算揭示了芳基硫醚体系的两个构象.Ar基团靠近Cp基团的芳基硫醚的Ti-S-Ar预测角度约为120 Ar组位于Cp组的远端时,测得的Ti-S-Ar角约为100°,并且通过分子和自然键轨道(NBO)分析来解释配体键的性质系统。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号