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  • Metalloproteins  (1)
  • quadruple  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cluster science 5 (1994), S. 37-66 
    ISSN: 1572-8862
    Keywords: Delta ; quadruple ; rotational barrier ; metal-metal ; bond
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract This review summarizes the contribution made to the field of delta bonds by Collman and co-workers. The delta (σ) bond is unique to metal-metal multipty bonded systems and has been the subject of several reviews (F. A. Cotton and R.A. Walton,Multiple Bomls Between Metal Atoms (Oxford University Press, New York, 1993), and references therein). Our contribution to this field is the measurement of the barrier to rotation about the axis of the metal-metal bond for a series of Mo and W porphyrin dimers. (J. P. Collman and L K. Woo (1984).Proc. Natl. Acad. Sci. USA 81, 2592-2596; J. P. Collman, J. M. Garner, R.T. Hembre, and Y. Ha (i992).J. Am. Chem. Soc. 114, 1292–1301). The barriers to rotation for the pórphyrin dimers are as follows: ΔG: rot,=9.8 to 10.7±0.5 kcal/mol for a series of [M(OEP-X)]2 dimers (X=CHO, NCO), ΔG: rot,= 10.5±0.5 kcal/mol for [Mo(TOEP)]2 and ΔG: rot= 12.9∓0.1 kcal/mol for [W(TOEP)], Each of these barriers reflects both the strength of the delta bond and steric interactions. The steric component is estimatëd to be small ( 〈5 kcal/mol); hence the barrier can be used as an estimate for the delta bond strength. These studies constitute the firstdirect experimental probe of the strength of delta bonds. These data for the rotational barriers in Mo and W dimers are of the same order of magnitude as the estimate of the 6 bond strength obtained using a generalized valenee bond treatment (6±3 kcal/mol) (D. C. Smith and W. A. Goddard 1II (1987).J. Am. Chem. Soc. 109, 5580-55831 and are in agreement with the recent estimate of the delta bond strength (⊃10kcal/mol) (M.D. Hopkins, H.B. Gray, and V.M. Miskowski (1987).Polyhedron 6, 705—714). In addition, this study demonstrates that the W (5d)σ bond is significantly stronger (⊃ 20%) than the anatogous Mo (4d)σ bond; this is consistent with the assertion that the greater radial expansion of 5 d orbitals can result in 5d-5d bonds which arestronger eren though they may belonger.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0570-0833
    Keywords: Metalloproteins ; Homogeneous catalysis ; Redox chemistry ; Porphyrin complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The role of metalloenzymes in important biological transformations has attracted increasing attention over the past several decades. Of the many chemical transformations mediated by enzymes, few are as challenging as multielectron redox reactions. Recent studies have revealed a partial structural and mechanistic description of these redox-active metalloenzymes, but there is much still to be learned regarding the mechanisms of substrate transformation. Due to the complexity of the metalloenzyme systems, simplified model systems are employed to mimic structural or functional features of the enzyme. In multielectron redox enzymes, several metals are probably in-volved in both substrate binding and the subsequent redox reactions. Thus, functional mimics of multielectron redox enzymes might also need two or more metal centers to be efficacious. The roles of multiple metal centers are to (1) increase the substrate's affinity for the catalyst, (2) increase the rate of electron transfer to the bound substrate, (3) increase the reactivity of the bound substrate, and (4) inhibit deleterious side reactions. Deter-mining the importance of each factor may help in the development of these catalysts. Cofacial metallodiporphyrins, because of the control they provide over the geometric and electronic properties of the synthetic reaction center, are ideal bimetallic model complexes. The knowledge gained from model studies will help in understanding the mechanisms of metalloenzymes and can be used to design new homogeneous catalysts to effect multielectron transformations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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