Tanner Christian, Manca Carine, Leutwyler Samuel
Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
Science. 2003 Dec 5;302(5651):1736-9. doi: 10.1126/science.1091708.
We characterized the entrance channel, reaction threshold, and mechanism of an excited-state H atom transfer reaction along a unidirectionally hydrogen-bonded "wire" -O-H...NH3...NH3...NH3...N. Excitation of supersonically cooled 7-hydroxyquinoline.(NH3)3 to its vibrationless S1 state produces no reaction, whereas excitation of ammonia-wire vibrations induces H atom transfer with a reaction threshold approximately 200 wave numbers. Further translocation steps along the wire produce the S1 state 7-ketoquinoline.(NH3)3 tautomer. Ab initio calculations show that proton and electron movement along the wire are closely coupled. The rate-controlling S1 state barriers arise from crossings of a pipi* with a Rydberg-type pisigma* state.
我们表征了沿单向氢键“链” -O-H...NH₃...NH₃...NH₃...N的激发态氢原子转移反应的入口通道、反应阈值和机理。将超声冷却的7-羟基喹啉·(NH₃)₃激发至其无振动的S₁态不会发生反应,而激发氨链振动会诱导氢原子转移,反应阈值约为200波数。沿链的进一步迁移步骤产生S₁态的7-酮基喹啉·(NH₃)₃互变异构体。从头算计算表明,质子和电子沿链的移动紧密耦合。速率控制的S₁态势垒源于ππ与里德堡型πσ态的交叉。