Halide Photoredox Chemistry

被引:157
作者
Troian-Gautier, Ludovic [1 ]
Turlington, Michael D. [1 ]
Wehlin, Sara A. M. [1 ]
Maurer, Andrew B. [1 ]
Brady, Matthew D. [1 ]
Swords, Wesley B. [1 ]
Meyer, Gerald J. [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; CHARGE-TRANSFER COMPLEXES; LASER FLASH-PHOTOLYSIS; SENSITIZED SOLAR-CELLS; EXCITED RUTHENIUM(II) COMPLEXES; RU(II) POLYPYRIDINE COMPLEXES; RADIATION-CHEMICAL OXIDATION; TRANSITION-METAL-COMPLEXES; I-I BONDS; AQUEOUS-SOLUTION;
D O I
10.1021/acs.chemrev.8b00732
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Halide photoredox chemistry is of both practical and fundamental interest. Practical applications have largely focused on solar energy conversion with hydrogen gas, through I-IX splitting, and electrical power generation, in regenerative photoelectrochemical and photovoltaic cells. On a more fundamental level, halide photoredox chemistry provides a unique means to generate and characterize one electron transfer chemistry that is intimately coupled with X-X bond-breaking and -forming reactivity. This review aims to deliver a background on the solution chemistry of I, Br, and Cl that enables readers to understand and utilize the most recent advances in halide photoredox chemistry research. These include reactions initiated through outer-sphere, halide-to-metal, and metal-to-ligand charge-transfer excited states. Kosower's salt, 1-methylpyridinium iodide, provides an early outer-sphere charge-transfer excited state that reports on solvent polarity. A plethora of new inner-sphere complexes based on transition and main group metal halide complexes that show promise for HX splitting are described. Long-lived charge-transfer excited states that undergo redox reactions with one or more halogen species are detailed. The review concludes with some key goals for future research that promise to direct the field of halide photoredox chemistry to even greater heights.
引用
收藏
页码:4628 / 4683
页数:56
相关论文
共 518 条
[1]   Decreased Interfacial Charge Recombination Rate Constants with N3-Type Sensitizers [J].
Abrahamsson, Maria ;
Johansson, Patrik G. ;
Ardo, Shane ;
Kopecky, Andrew ;
Galoppini, Elena ;
Meyer, Gerald J. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (11) :1725-1728
[2]   Direct C-C Bond Formation from Alkanes Using Ni-Photoredox Catalysis [J].
Ackerman, Laura K. G. ;
Alvarado, Jesus I. Martinez ;
Doyle, Abigail G. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (43) :14059-14063
[3]   EVALUATION OF THE STABILITY CONSTANT OF CL-2(CENTER-DOT-) IN NEUTRAL AQUEOUS-SOLUTION [J].
ADAMS, DJ ;
BARLOW, S ;
BUXTON, GV ;
MALONE, TM ;
SALMON, GA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (18) :3303-3305
[4]   Cyclometalation Using d-Block Transition Metals: Fundamental Aspects and Recent Trends [J].
Albrecht, Martin .
CHEMICAL REVIEWS, 2010, 110 (02) :576-623
[5]   Kinetic study of the reactions of chlorine atoms and Cl2•- radical anions in aqueous solutions.: 1.: Reaction with benzene [J].
Alegre, ML ;
Geronés, M ;
Rosso, JA ;
Bertolotti, SG ;
Braun, AM ;
Mártire, DO ;
Gonzalez, MC .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (14) :3117-3125
[6]   Microbial Contribution to Global Iodine Cycling: Volatilization, Accumulation, Reduction, Oxidation, and Sorption of Iodine [J].
Amachi, Seigo .
MICROBES AND ENVIRONMENTS, 2008, 23 (04) :269-276
[7]   PULSE RADIOLYSIS STUDIES OF AQUEOUS SODIUM CHLORIDE SOLUTIONS [J].
ANBAR, M ;
THOMAS, JK .
JOURNAL OF PHYSICAL CHEMISTRY, 1964, 68 (12) :3829-&
[8]   CHEMICAL MODIFICATION OF A TITANIUM(IV) OXIDE ELECTRODE TO GIVE STABLE DYE SENSITIZATION WITHOUT A SUPERSENSITIZER [J].
ANDERSON, S ;
CONSTABLE, EC ;
DAREEDWARDS, MP ;
GOODENOUGH, JB ;
HAMNETT, A ;
SEDDON, KR ;
WRIGHT, RD .
NATURE, 1979, 280 (5723) :571-573
[9]   OPTICAL-SPECTRA OF DIBROMIDE AND DIIODIDE IONS IN MATRIX-ISOLATED M+BR-2-AND M+I-2-SPECIES [J].
ANDREWS, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (08) :2152-2156
[10]  
[Anonymous], ADV INORGANIC CHEM