A Novel N,P,C Cage Complex Formed by Rearrangement of a Tricyclic Phosphirane Complex: On the Importance of Non-covalent Interactions

被引:14
|
作者
Nesterov, Vitaly [1 ]
Espinosa, Arturo [2 ]
Schnakenburg, Gregor [1 ]
Streubel, Rainer [1 ]
机构
[1] Univ Bonn, Inst Anorgan Chem, D-53121 Bonn, Germany
[2] Univ Murcia, Fac Quim, Dept Quim Organ, E-30100 Murcia, Spain
关键词
cage compounds; noncovalent interactions; P ligands; rearrangement; tungsten; NITRILIUM PHOSPHANE-YLIDE; 3+2 CYCLOADDITION; CHEMISTRY; PSEUDOPOTENTIALS; DERIVATIVES; PROGRAM; MODEL; ATOMS;
D O I
10.1002/chem.201305061
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction of Li/Cl P-CPh3 phosphinidenoid tungsten(0) complex 2 with dimethylcyanamide afforded tricyclic phosphirane complex 4, an unprecedented rearrangement of which led to the novel N,P,C cage complex 6. On the basis of DFT calculations, formation and intramolecular [3+2] cycloaddition of the transient nitrilium phosphane ylide complex 3 to a phenyl ring of the triphenylmethyl substituent to give 4 is proposed. Furthermore, theoretical evidence for terminal N-amidinophosphinidene complex 7, formed by [2+1] cycloelimination from 4, is provided, and the role of the electronic structure and non-covalent interactions of intermediate 7 discussed.
引用
收藏
页码:7010 / 7016
页数:7
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