Coordination Chemistry of Cyclic Disilylated Stannylenes and Plumbylenes to Group 4 Metallocenes
Author(s) -
Henning Arp,
Judith Baumgartner,
Christoph Marschner,
P. Zark,
Thomas Müller
Publication year - 2012
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja301547x
Subject(s) - chemistry , metallocene , phosphine , adduct , magnesium , group (periodic table) , titanium , crystallography , medicinal chemistry , stereochemistry , organic chemistry , catalysis , polymer , polymerization
Reduction of group 4 metallocene dichlorides with magnesium in the presence of cyclic disilylated stannylene or plumbylene phosphine adducts yielded the respective metallocene tetrylene phosphine complexes. Under the same conditions the use of the respective dimerized stannylene or plumbylene gave metallocene ditetrylene complexes. A computational analysis of these reactions revealed for all investigated compounds multiple-bonded character for the M-E(II) linkage, which can be rationalized in the case of the monotetrylene complex with the classical σ-donor/π-acceptor interaction. The strength of the M-E(II) bond increases descending group 4 and decreases going from Sn to its heavier congener Pb. The weakness of the Ti-E(II) bonds is caused by the significantly reduced ability of the titanium atom for d-p π-back-bonding.
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