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Updated: Oct 3, 2026

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR
Published on: December 16, 2013
Effect of Conformational Constraints on Gated Electron Transfer Kinetics. 2. Copper(II/I) Complexes with
Brian C. Dunn1, L. A. Ochrymowycz, D. B. Rorabacher
1Departments of Chemistry, Wayne State University, Detroit, Michigan 48202, and University of Wisconsin-Eau Claire, Eau Claire, Wisconsin 54701.
Abstract:
Kinetic studies have been conducted in acetonitrile on the electron-transfer reactions of five copper(II/I) complexes involving ligands in which either a benzene or a cyclohexane ring, or both, have been substituted into the ligand backbone of the 14-membered tetrathiamacrocycle [14]aneS(4). The specific ligands utilized in this work include 2,3-benzo-1,4,8,11-tetrathiacyclotetradecane (bz-[14]aneS(4)), 2,3-trans-cyclohexano-1,4,8,11-tetrathiacyclotetradecane (trans-cyhx-[14]aneS(4)), 2,3-benzo-9,10-trans-cyclohexano-1,4,8,11-tetrathiacyclotetradecane (bz,trans-cyhx-[14]aneS(4)), 2,3-benzo-9,10-cis-cyclohexano-1,4,8,11-tetrathiacyclotetradecane (bz,cis-cyhx-[14]aneS(4)), and 2,3-cis-9,10-trans-dicyclohexano-1,4,8,11-tetrathiacyclotetradecane (cis, trans-dicyhx-[14]aneS(4)). Each Cu(II/I)L system has been reacted with three separate reducing agents and three separate oxidizing agents to examine the effect of driving force upon the kinetic parameters. The Marcus relationship has been applied to each cross-reaction rate constant to estimate the apparent self-exchange rate constant, k(11), for each Cu(II/I)L system. For all but one of the five systems, the k(11) values obtained from the three reduction reactions are in virtual agreement with the corresponding value obtained for the oxidation reaction with the smallest driving force. As the driving force for Cu(I)L oxidation increases, a smaller k(11) value is calculated for each system. This behavior is consistent with our previously proposed dual-pathway square scheme mechanism in which a significant conformational change occurs as a separate step preceding electron transfer in the case of Cu(I)L oxidation. Although direct observation of conformationally-gated electron transfer was not attained for any of the five systems included in the current work, limits for the rate constant for conformational change have been estimated from the conditions required to change the apparent pathway for the oxidation kinetics. These limits show that the Cu(I)L complex involving a single phenyl substituent (bz-[14]aneS(4)) exhibits a much slower conformational change than do any of the other systems included in this study. The implications of this observation are discussed.
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