PHOTOCATALYTIC REDUCTION OF PHENACYL HALIDES BY 9,10-DIHYDRO-10-METHYLACRIDINE - CONTROL BETWEEN THE REDUCTIVE AND OXIDATIVE QUENCHING PATHWAYS OF TRIS(BIPYRIDINE)RUTHENIUM COMPLEX UTILIZING AN ACID CATALYSIS
PHOTOCATALYTIC REDUCTION OF PHENACYL HALIDES BY 9,10-DIHYDRO-10-METHYLACRIDINE - CONTROL BETWEEN THE REDUCTIVE AND OXIDATIVE QUENCHING PATHWAYS OF TRIS(BIPYRIDINE)RUTHENIUM COMPLEX UTILIZING AN ACID CATALYSIS
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DOI:
10.1021/j100365a039
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发表时间:
1990-01-25
影响因子:
--
通讯作者:
TANAKA, T
中科院分区:
文献类型:
--
作者:
FUKUZUMI, S;MOCHIZUKI, S;TANAKA, T
As quenching via electron transfer has becomewell established, it has been frequently found that the same excited-state substrate can be quenched by electron donors and acceptors. 2, 3 A number of works discussed here involve reactions initiated by excitation of poly (pyridyl) ruthenium (II) complexes, typically,[Ru (bpy) 3] 2+(bpy= 2, 2'-bipyridine). 1 2 34568 The excited state,[Ru (bpy) 3] 2+*, can be efficiently quenched by electron donors such as amines and aromatic ethers5, 6 or electron acceptors such as bipyridyl dications (eg, methylviologen) 7 and a series of nitro aromatics. 8* While these processes can occur very efficiently, they are generally followed by energy-wasting back-electron-transfer reactions that also usually occur more efficiently such that the frequent result is no net chemical reactions. 2, 3 Net chemical reactions can be achieved when the reductive quenching of [Ru (bpy) 3] 2+* by electron donors Dred (eq 1) is followed by the irreversible reduction