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Wenbo E, Ph.D.

Affiliations: 
2004 University of Houston, Houston, TX, United States 
Area:
Analytical Chemistry
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"Wenbo E"
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Karl M. Kadish grad student 2004 University of Houston
 (Redox properties of electroactive porphyrin-based components for 'molecular electronics'.)

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Hao E, Zhang M, E W, et al. (2008) Synthesis and spectroelectrochemistry of N-cobaltacarborane porphyrin conjugates. Bioconjugate Chemistry. 19: 2171-81
Fukuzumi S, Ohkubo K, Zhu W, et al. (2008) Androgynous porphyrins. Silver(II) quinoxalinoporphyrins act as both good electron donors and acceptors. Journal of the American Chemical Society. 130: 9451-8
Sintic PJ, E W, Ou Z, et al. (2008) Control of the site and potential of reduction and oxidation processes in pi-expanded quinoxalinoporphyrins. Physical Chemistry Chemical Physics : Pccp. 10: 268-80
Zhang M, E W, Ohkubo K, et al. (2008) Electron-transfer and acid-base properties of a two-electron oxidized form of quaterpyrrole that acts as both an electron donor and an acceptor. The Journal of Physical Chemistry. A. 112: 1633-42
Sintic PJ, E W, Ou Z, et al. (2008) Control of the site and potential of reduction and oxidation processes in pi-expanded quinoxalinoporphyrins. Physical Chemistry Chemical Physics : Pccp. 10: 515-27
E W, Kadish KM, Sintic PJ, et al. (2008) Control of the orbital delocalization and implications for molecular rectification in the radical anions of porphyrins with coplanar 90 degrees and 180 degrees beta,beta'-fused extensions. The Journal of Physical Chemistry. A. 112: 556-70
Ou Z, E W, Zhu W, et al. (2007) Effect of axial ligands and macrocyclic structure on redox potentials and electron-transfer mechanisms of SnIV porphyrins. Inorganic Chemistry. 46: 10840-9
Kadish KM, E W, Sintic PJ, et al. (2007) Quinoxalino[2,3-b']porphyrins behave as pi-expanded porphyrins upon one-electron reduction: broad control of the degree of delocalization through substitution at the macrocycle periphery. The Journal of Physical Chemistry. B. 111: 8762-74
Kadish KM, E W, Zhan R, et al. (2007) Porphyrin-diones and porphyrin-tetraones: reversible redox units being localized within the porphyrin macrocycle and their effect on tautomerism. Journal of the American Chemical Society. 129: 6576-88
E W, Ohkubo K, Sanchez-Garcia D, et al. (2007) Electron-transfer oxidation properties of substituted bi-, ter-, and quaterpyrroles. The Journal of Physical Chemistry. B. 111: 4320-6
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