Selective photocatalytic reduction of CO2 to CO mediated by a [FeFe]-hydrogenase model with a 1,2-phenylene S-to-S bridge

Halmann, 1978, Nature, 275, 115, 10.1038/275115a0 Inoue, 1979, Nature, 277, 637, 10.1038/277637a0 Bonin, 2017, Coord. Chem. Rev., 334, 184, 10.1016/j.ccr.2016.09.005 Takeda, 2017, ACS Catal., 7, 70, 10.1021/acscatal.6b02181 Elgrishi, 2017, Chem. Soc. Rev., 46, 761, 10.1039/C5CS00391A Dalle, 2019, Chem. Rev., 119, 2752, 10.1021/acs.chemrev.8b00392 Takeda, 2014, Chem. Commun., 50, 1491, 10.1039/C3CC48122K Torralba-Peñalver, 2015, ACS Catal., 5, 6138, 10.1021/acscatal.5b01546 Cheung, 2016, Inorg. Chem., 55, 3192, 10.1021/acs.inorgchem.6b00379 Zhang, 2016, Appl. Catal. A, 522, 145, 10.1016/j.apcata.2016.04.035 Bonin, 2014, ChemCatChem, 6, 3200, 10.1002/cctc.201402515 Takeda, 2016, J. Am. Chem. Soc., 138, 4354, 10.1021/jacs.6b01970 Alsabeh, 2016, Catal. Sci. Technol., 6, 3623, 10.1039/C5CY01129A Rosas-Hernández, 2016, Chem. Commun., 52, 8393, 10.1039/C6CC01671E Rao, 2017, ChemSusChem, 10, 4447, 10.1002/cssc.201701467 Rao, 2017, Nature, 548, 74, 10.1038/nature23016 Bonin, 2014, J. Am. Chem. Soc., 136, 16768, 10.1021/ja510290t Rosas-Hernández, 2017, Green Chem., 19, 2356, 10.1039/C6GC03527B Rao, 2017, Chem. Commun., 53, 2830, 10.1039/C6CC09967J Guo, 2016, J. Am. Chem. Soc., 138, 9413, 10.1021/jacs.6b06002 Grodkowski, 2000, J. Phys. Chem. A, 104, 11332, 10.1021/jp002709y Chen, 2015, J. Am. Chem. Soc., 137, 10918, 10.1021/jacs.5b06535 Grodkowski, 2002, J. Phys. Chem. A, 106, 4772, 10.1021/jp013668o Chan, 2015, Chem. Commun., 51, 7799, 10.1039/C5CC00566C Zhang, 2015, J. Phys. Chem. C, 119, 4645, 10.1021/jp5127738 Yang, 2016, Chem. Sci., 7, 3123, 10.1039/C5SC04458H Wang, 2016, Catal. Sci. Technol., 6, 7408, 10.1039/C6CY01265E Liu, 2018, Chem. Commun., 54, 11308, 10.1039/C8CC04892D Zhu, 2018, Dalton Trans., 47, 13142, 10.1039/C8DT02148A Leung, 2019, Nat. Catal., 2, 354, 10.1038/s41929-019-0254-2 Ouyang, 2017, Inorg. Chem., 56, 7307, 10.1021/acs.inorgchem.7b00566 Ouyang, 2017, Angew. Chem. Int. Ed., 56, 738, 10.1002/anie.201610607 Ouyang, 2018, Angew. Chem. Int. Ed., 57, 16480, 10.1002/anie.201811010 Thoi, 2013, J. Am. Chem. Soc., 135, 14413, 10.1021/ja4074003 Shirley, 2019, J. Am. Chem. Soc., 141, 6617, 10.1021/jacs.9b00937 Hong, 2017, J. Am. Chem. Soc., 139, 6538, 10.1021/jacs.7b01956 Kuehnel, 2017, J. Am. Chem. Soc., 139, 7217, 10.1021/jacs.7b00369 Neri, 2016, Chem. Commun., 52, 14200, 10.1039/C6CC08590C Guo, 2017, ChemSusChem, 10, 4009, 10.1002/cssc.201701354 Hong, 2019, J. Am. Chem. Soc., 141, 20309, 10.1021/jacs.9b10597 Steinlechner, 2019, ACS Catal., 9, 2091, 10.1021/acscatal.8b03548 Jeoung, 2007, Science, 318, 1461, 10.1126/science.1148481 Bruckmeier, 2012, Dalton Trans., 41, 5026, 10.1039/c2dt30273j Reithmeier, 2014, Dalton Trans., 43, 13259, 10.1039/C4DT01717J Mochizuki, 1996, Inorg. Chem., 35, 5132, 10.1021/ic960208e Cheng, 2018, ACS Catal., 9, 768, 10.1021/acscatal.8b03921 Cabeza, 1998, Organometallics, 17, 1471, 10.1021/om970922j Gloaguen, 2001, J. Am. Chem. Soc., 123, 12518, 10.1021/ja016071v Juris, 1981, Helv. Chim. Acta, 64, 2175, 10.1002/hlca.19810640723 Prier, 2013, Chem. Rev., 113, 5322, 10.1021/cr300503r Tamaki, 2013, J. Catal., 304, 22, 10.1016/j.jcat.2013.04.002 Hasegawa, 2006, Tetrahedron, 62, 6581, 10.1016/j.tet.2006.03.061 Felton, 2007, J. Am. Chem. Soc., 129, 12521, 10.1021/ja073886g Wright, 2012, Dalton Trans., 41, 73, 10.1039/C1DT11428J Ngo, 2017, J. Am. Chem. Soc., 139, 2604, 10.1021/jacs.6b08776 Haviv, 2018, J. Am. Chem. Soc., 140, 12451, 10.1021/jacs.8b05658 Liu, 2013, Chem. Commun., 49, 4743, 10.1039/c3cc39008j Probst, 2010, Inorg. Chem., 49, 6453, 10.1021/ic100036v