Literature DB >> 14514296

Symmetry and geometry considerations of atom transfer: deoxygenation of (silox)3WNO and R3PO (R = Me, Ph, (t)Bu) by (silox)3M (M = V, NbL (L = PMe3, 4-picoline), Ta; silox = (t)Bu3SiO).

Adam S Veige1, LeGrande M Slaughter, Emil B Lobkovsky, Peter T Wolczanski, Nikita Matsunaga, Stephen A Decker, Thomas R Cundari.   

Abstract

Deoxygenations of (silox)(3)WNO (12) and R(3)PO (R = Me, Ph, (t)Bu) by M(silox)(3) (1-M; M = V, NbL (L = PMe(3), 4-picoline), Ta; silox = (t)Bu(3)SiO) reflect the consequences of electronic effects enforced by a limiting steric environment. 1-Ta rapidly deoxygenated R(3)PO (23 degrees C; R = Me (DeltaG degrees (rxn)(calcd) = -47 kcal/mol), Ph) but not (t)Bu(3)PO (85 degrees, >2 days), and cyclometalation competed with deoxygenation of 12 to (silox)(3)WN (11) and (silox)(3)TaO (3-Ta; DeltaG degrees (rxn)(calcd) = -100 kcal/mol). 1-V deoxygenated 12 slowly and formed stable adducts (silox)(3)V-OPR(3) (3-OPR(3)) with OPR(3). 1-Nb(4-picoline) (S = 0) and 1-NbPMe(3) (S = 1) deoxygenated R(3)PO (23 degrees C; R = Me (DeltaG degrees (rxn)(calcd from 1-Nb) = -47 kcal/mol), Ph) rapidly and 12 slowly (DeltaG degrees (rxn)(calcd) = -100 kcal/mol), and failed to deoxygenate (t)Bu(3)PO. Access to a triplet state is critical for substrate (EO) binding, and the S --> T barrier of approximately 17 kcal/mol (calcd) hinders deoxygenations by 1-Ta, while 1-V (S = 1) and 1-Nb (S --> T barrier approximately 2 kcal/mol) are competent. Once binding occurs, significant mixing with an (1)A(1) excited state derived from population of a sigma-orbital is needed to ensure a low-energy intersystem crossing of the (3)A(2) (reactant) and (1)A(1) (product) states. Correlation of a reactant sigma-orbital with a product sigma-orbital is required, and the greater the degree of bending in the (silox)(3)M-O-E angle, the more mixing energetically lowers the intersystem crossing point. The inability of substrates EO = 12 and (t)Bu(3)PO to attain a bent 90 degree angle M-O-E due to sterics explains their slow or negligible deoxygenations. Syntheses of relevant compounds and ramifications of the results are discussed. X-ray structural details are provided for 3-OPMe(3) (90 degree angle V-O-P = 157.61(9) degrees), 3-OP(t)Bu(3) ( 90 degree angle V-O-P = 180 degrees ), 1-NbPMe(3), and (silox)(3)ClWO (9).

Entities:  

Year:  2003        PMID: 14514296     DOI: 10.1021/ic0300114

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  6 in total

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Journal:  J Am Chem Soc       Date:  2010-03-31       Impact factor: 15.419

2.  Synthesis, Characterization, and Reactions of Isolable (β-Diketiminato)Nb(III) Imido Complexes.

Authors:  Neil C Tomson; John Arnold; Robert G Bergman
Journal:  Organometallics       Date:  2010-11-08       Impact factor: 3.876

3.  Sulfur K-edge X-ray absorption spectroscopy and density functional calculations on Mo(IV) and Mo(VI)=O bis-dithiolenes: insights into the mechanism of oxo transfer in DMSO reductase and related functional analogues.

Authors:  Adam L Tenderholt; Jun-Jieh Wang; Robert K Szilagyi; Richard H Holm; Keith O Hodgson; Britt Hedman; Edward I Solomon
Journal:  J Am Chem Soc       Date:  2010-06-23       Impact factor: 15.419

4.  New Routes to Low-Coordinate Iron Hydride Complexes: The Binuclear Oxidative Addition of H(2).

Authors:  Thomas R Dugan; Patrick L Holland
Journal:  J Organomet Chem       Date:  2009-08       Impact factor: 2.369

5.  Structure-function analysis of 2-keto-3-deoxy-D-glycero-D-galactonononate-9-phosphate phosphatase defines specificity elements in type C0 haloalkanoate dehalogenase family members.

Authors:  Zhibing Lu; Liangbing Wang; Debra Dunaway-Mariano; Karen N Allen
Journal:  J Biol Chem       Date:  2008-11-05       Impact factor: 5.157

6.  (Penta-fluoro-propionato-κO)tetra-kis-(trimethyl-phosphine oxide-κO)copper(II) penta-fluoro-propionate.

Authors:  Iwona B Szymańska; Liliana Dobrzańska
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-08-11
  6 in total

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