Kowert Bruce A, Fehr Michael J, Sheaff Pamela J
Department of Chemistry, Saint Louis University, 3501 Laclede Avenue, St. Louis, Missouri 63103, USA.
Inorg Chem. 2008 Jul 7;47(13):5696-701. doi: 10.1021/ic702436x. Epub 2008 Jun 7.
The rate constant, k, for the homogeneous electron transfer (self-exchange) reaction between the diamagnetic bis(maleonitriledithiolato)nickel dianion, [Ni(mnt) 2] (2-), and the paramagnetic monoanion, [Ni(mnt) 2] (1-), has been determined in acetone and nitromethane (CH 3NO 2) using (13)C NMR line widths at 22 degrees C (mnt = 1,2-S 2C 2(CN) 2). The values of k (2.91 x 10 (6) M (-1) s (-1) in acetone, 5.78 x 10 (6) M (-1) s (-1) in CH 3NO 2) are faster than those for the electron transfer reactions of other Ni(III,II) couples; the structures of [Ni(mnt) 2] (1-) and [Ni(mnt) 2] (2-) allow for a favorable overlap that lowers the free energy of activation. The values of k are consistent with the predictions of Marcus theory. In addition to k, the spin-lattice relaxation time, T 1e, of [Ni(mnt) 2] (1-) is obtained from the NMR line width analysis; the values are consistent with those predicted by spin relaxation theory.
在22℃下,利用(13)C NMR线宽,已在丙酮和硝基甲烷(CH3NO2)中测定了抗磁性双(马来腈二硫醇根)镍二价阴离子[Ni(mnt)2](2-)和顺磁性单阴离子[Ni(mnt)2](1-)之间均相电子转移(自交换)反应的速率常数k(mnt = 1,2-S2C2(CN)2)。k的值(在丙酮中为2.91×10(6)M(-1)s(-1),在CH3NO2中为5.78×10(6)M(-1)s(-1))比其他Ni(III,II)偶合的电子转移反应的值要快;[Ni(mnt)2](1-)和[Ni(mnt)2](2-)的结构允许有利的重叠,从而降低了活化自由能。k的值与马库斯理论的预测一致。除了k之外,还通过NMR线宽分析获得了[Ni(mnt)2](1-)的自旋晶格弛豫时间T1e;这些值与自旋弛豫理论预测的值一致。