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Zr−E π-Bonding in Complexes Derived from E−H Additions to Cp2Zr(P(C6H2-2,4,6-t-Bu3))(PMe3)
Additions of PhEH (E = O, S), PhEH2 (E = N, P), MesPH2, and Ph2PH to Cp2Zr(PR*)(PMe3) (2) provide a facile route to complexes of the form Cp2Zr(PHR*)(ER) (R* = 2,4,6-t-Bu-C6H2; ER = OPh (3), SPh (4), NHPh (5), PHPh (6), PHMes (7), PPh2 (8)). Variable-temperature NMR studies are consistent with facil...
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Published in: | Organometallics 1996-10, Vol.15 (20), p.4223-4227 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Additions of PhEH (E = O, S), PhEH2 (E = N, P), MesPH2, and Ph2PH to Cp2Zr(PR*)(PMe3) (2) provide a facile route to complexes of the form Cp2Zr(PHR*)(ER) (R* = 2,4,6-t-Bu-C6H2; ER = OPh (3), SPh (4), NHPh (5), PHPh (6), PHMes (7), PPh2 (8)). Variable-temperature NMR studies are consistent with facile metal-mediated inversion at phosphorus as well as rapid rotation about the Zr−E bonds at room temperature. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om960314o |