Editing Photochemical reduction of carbon dioxide to formic acid

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[[Category:Photocatalytic CO2 conversion to HCOOH]]
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|date=2023-02-17
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{{#doiinfobox: 10.1039/D0GC04040A }}

=== Review ===
{{#literature:|doi=10.1039/D0GC04040A}}

===== Table 1 =====
35 J. Hawecker, J.-M. Lehn and R. Ziessel, ChemComm, 1985, 56, DOI: 10.1039/C39850000056 .

36 J.-M. Lehn and R. Ziessel, J. Organomet. Chem., 1990, 382, 157.

42 [[Photochemical Reduction of Carbon Dioxide to Formic Acid using Ruthenium(II)-Based Catalysts and Visible Light|A. Rosas-Hernández, H. Junge and M. Beller, ChemCatChem, 2015, 7, 3316.]] (complete)

46 [[Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction|J. Rohacova and O. Ishitani, Chem. Sci., 2016, 7, 6728.]] (complete)

48 [[Function-Integrated Ru Catalyst for Photochemical CO2 Reduction|S. K. Lee, M. Kondo, M. Okamura, T. Enomoto, G. Nakamura and S. Masaoka, J. Am. Chem. Soc., 2018, 140, 16899.]] (complete)

49 [[Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands|Y. Hameed, G. K. Rao, J. S. Ovens, B. Gabidullin and D. Richeson, ChemSusChem, 2019, 12, 3453.]] (complete)

51 [[Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes|Y. Arikawa, I. Tabata, Y. Miura, H. Tajiri, Y. Seto, S. Horiuchi, E. Sakuda and K. Umakoshi, Chem. – Eur. J., 2020, 26, 5603.]] (complete) 

===== Table2 =====
52 D. Behar, T. Dhanasekaran, P. Neta, C. M. Hosten, D. Ejeh, P. Hambright and E. Fujita, J. Phys. Chem. A, 1998, 102, 2870.

55 Z. Guo, G. Chen, C. Cometto, B. Ma, H. Zhao, T. Groizard, L. Chen, H. Fan, W.-L. Man, S.-M. Yiu, K.-C. Lau, T.-C. Lau and M. Robert, Nat. Catal., 2019, 2, 801. (No access)

===== Table 3 =====
57 [[Photocatalytic CO2 reduction using a Mn complex as a catalyst|H. Takeda, H. Koizumi, K. Okamoto and O. Ishitani, ChemComm, 2014, 50, 1491.]] (complete)

59 [[Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH|M. Stanbury, J.-D. Compain, M. Trejo, P. Smith, E. Gouré and S. Chardon-Noblat, Electrochim. Acta, 2017, 240, 288.]] (complete)

62 [[Highly Efficient and Robust Photocatalytic Systems for CO2 Reduction Consisting of a Cu(I) Photosensitizer and Mn(I) Catalysts|H. Takeda, H. Kamiyama, K. Okamoto, M. Irimajiri, T. Mizutani, K. Koike, A. Sekine and O. Ishitani, J. Am. Chem. Soc., 2018, 140, 17241.]] (complete)

58 [[Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3|P. L. Cheung, C. W. Machan, A. Y. S. Malkhasian, J. Agarwal and C. P. Kubiak, Inorg. Chem., 2016, 55, 3192.]] (complete)

46 [[Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction|J. Rohacova and O. Ishitani, Chem. Sci., 2016, 7, 6728.]] (complete)

60 [[Visible light driven reduction of CO2 catalyzed by an abundant manganese catalyst with zinc porphyrin photosensitizer|J.-X. Zhang, C.-Y. Hu, W. Wang, H. Wang and Z.-Y. Bian, Appl. Catal., A, 2016, 522, 145.]] (complete)

===== Table 4 =====
63 [[Molecular Catalysis of the Electrochemical and Photochemical Reduction of CO2 with Earth-Abundant Metal Complexes. Selective Production of CO vs HCOOH by Switching of the Metal Center|L. Chen, Z. Guo, X.-G. Wei, C. Gallenkamp, J. Bonin, E. Anxolabéhère-Mallart, K.-C. Lau, T.-C. Lau and M. Robert, J. Am. Chem. Soc., 2015, 137, 10918.]] (complete)

65 [[Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction|T. Fogeron, P. Retailleau, L.-M. Chamoreau, Y. Li and M. Fontecave, Angew. Chem., Int. Ed., 2018, 57, 17033.]] (complete)

67 [[Ir(tpy)(bpy)Cl as a Photocatalyst for CO2 Reduction under Visible-Light Irradiation|S. Sato and T. Morikawa, ChemPhotoChem, 2018, 2, 207.]] (complete)

69 [[Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid|K. Kamada, J. Jung, T. Wakabayashi, K. Sekizawa, S. Sato, T. Morikawa, S. Fukuzumi and S. Saito, J. Am. Chem. Soc., 2020, 142, 10261.]] (complete)

71 [[An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2|Y. Hameed, P. Berro, B. Gabidullin and D. Richeson, ChemComm, 2019, 55, 11041.]] (complete)

===== Table 5 - metal-free PS with Co-, Mn-, Ru-catalysts =====
76 S. Matsuoka, K. Yamamoto, C. Pac and S. Yanagida, Chem. Lett., 1991, 20, 2099.

22 S. Matsuoka, K. Yamamoto, T. Ogata, M. Kusaba, N. Nakashima, E. Fujita and S. Yanagida, J. Am. Chem. Soc., 1993, 115, 601.

80 T. Ogata, Y. Yamamoto, Y. Wada, K. Murakoshi, M. Kusaba, N. Nakashima, A. Ishida, S. Takamuku and S. Yanagida, J. Phys. Chem., 1995, 99, 11916.

81 D. J. Boston, C. Xu, D. W. Armstrong and F. M. MacDonnell, J. Am. Chem. Soc., 2013, 135, 16252.

85 S. E. Lee, A. Nasirian, Y. E. Kim, P. T. Fard, Y. Kim, B. Jeong, S.-J. Kim, J.-O. Baeg and J. Kim, J. Am. Chem. Soc., 2020, 142, 19142.

===== Table 6 - Supramolecular catalysts and PS =====
90 Y. Tamaki, T. Morimoto, K. Koike and O. Ishitani, Proc. Natl. Acad. Sci. U. S. A., 2012, 109, 15673.

91 Y. Tamaki, K. Koike and O. Ishitani, Chem. Sci., 2015, 6, 7213.

92 Y. Tamaki and O. Ishitani, Faraday Discuss., 2017, 198, 319.

93 D. C. Fabry, H. Koizumi, D. Ghosh, Y. Yamazaki, H. Takeda, Y. Tamaki and O. Ishitani, Organometallics, 2020, 39, 1511.

===== Table 7 - catalysts linked to metal-based semiconductors =====
94 S. Sato, T. Morikawa, S. Saeki, T. Kajino and T. Motohiro, Angew. Chem., Int. Ed., 2010, 49, 5101.

95 T. M. Suzuki, H. Tanaka, T. Morikawa, M. Iwaki, S. Sato, S. Saeki, M. Inoue, T. Kajino and T. Motohiro, ChemComm, 2011, 47, 8673.

20 S. Sato, T. Arai, T. Morikawa, K. Uemura, T. M. Suzuki, H. Tanaka and T. Kajino, J. Am. Chem. Soc., 2011, 133, 15240.

97 T. Arai, S. Sato, T. Kajino and T. Morikawa, Energy Environ. Sci., 2013, 6, 1274.

21 K. Sekizawa, K. Maeda, K. Domen, K. Koike and O. Ishitani, J. Am. Chem. Soc., 2013, 135, 4596.

98 F. Yoshitomi, K. Sekizawa, K. Maeda and O. Ishitani, ACS Appl. Mater. Interfaces, 2015, 7, 13092.

102 R. Kuriki, T. Ichibha, K. Hongo, D. Lu, R. Maezono, H. Kageyama, O. Ishitani, K. Oka and K. Maeda, J. Am. Chem. Soc., 2018, 140, 6648.

101 A. Nakada, R. Kuriki, K. Sekizawa, S. Nishioka, J. J. M. Vequizo, T. Uchiyama, N. Kawakami, D. Lu, A. Yamakata, Y. Uchimoto, O. Ishitani and K. Maeda, ACS Catal., 2018, 8, 9744.

103 T. Oshima, T. Ichibha, K. S. Qin, K. Muraoka, J. J. M. Vequizo, K. Hibino, R. Kuriki, S. Yamashita, K. Hongo, T. Uchiyama, K. Fujii, D. Lu, R. Maezono, A. Yamakata, H. Kato, K. Kimoto, M. Yashima, Y. Uchimoto, M. Kakihana, O. Ishitani, H. Kageyama and K. Maeda, Angew. Chem., Int. Ed., 2018, 57, 8154.

100 K. Muraoka, H. Kumagai, M. Eguchi, O. Ishitani and K. Maeda, ChemComm, 2016, 52, 7886.

107 K. Muraoka, T. Uchiyama, D. Lu, Y. Uchimoto, O. Ishitani and K. Maeda, Bull. Chem. Soc. Jpn., 2019, 92, 124.

106 K. Muraoka, M. Eguchi, O. Ishitani, F. Cheviré and K. Maeda, J. Energy Chem., 2021, 55, 176.

===== Table 8 - catalysts linked to metal-free semiconductors =====
109 K. Maeda, K. Sekizawa and O. Ishitani, ChemComm, 2013, 49, 10127.

111 R. Kuriki, K. Sekizawa, O. Ishitani and K. Maeda, Angew. Chem., Int. Ed., 2015, 54, 2406.

112 R. Kuriki, H. Matsunaga, T. Nakashima, K. Wada, A. Yamakata, O. Ishitani and K. Maeda, J. Am. Chem. Soc., 2016, 138, 5159.

113 R. Kuriki, M. Yamamoto, K. Higuchi, Y. Yamamoto, M. Akatsuka, D. Lu, S. Yagi, T. Yoshida, O. Ishitani and K. Maeda, Angew. Chem., Int. Ed., 2017, 56, 4867.

116 K. Maeda, D. An, R. Kuriki, D. Lu and O. Ishitani, Beilstein J. Org. Chem., 2018, 14, 1806.[[Category:Review]]
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