Photochemical reduction of carbon dioxide to formic acid

DOI needed

Date: 2023-02-17 Author: ChN This page is about a dataset that does not have a DOI or other persistent identifier. Please consider saving your dataset in a repository that provides a persistent identifier or add an identifier on this page.

Review

[Pro21]

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 A. Rosas-Hernández, H. Junge and M. Beller, ChemCatChem, 2015, 7, 3316. (complete)

46 J. Rohacova and O. Ishitani, Chem. Sci., 2016, 7, 6728. (complete)

48 S. K. Lee, M. Kondo, M. Okamura, T. Enomoto, G. Nakamura and S. Masaoka, J. Am. Chem. Soc., 2018, 140, 16899. (complete)

49 Y. Hameed, G. K. Rao, J. S. Ovens, B. Gabidullin and D. Richeson, ChemSusChem, 2019, 12, 3453. (complete)

51 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 H. Takeda, H. Koizumi, K. Okamoto and O. Ishitani, ChemComm, 2014, 50, 1491. (complete)

59 M. Stanbury, J.-D. Compain, M. Trejo, P. Smith, E. Gouré and S. Chardon-Noblat, Electrochim. Acta, 2017, 240, 288. (complete)

62 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 P. L. Cheung, C. W. Machan, A. Y. S. Malkhasian, J. Agarwal and C. P. Kubiak, Inorg. Chem., 2016, 55, 3192. (complete)

46 J. Rohacova and O. Ishitani, Chem. Sci., 2016, 7, 6728. (complete)

60 J.-X. Zhang, C.-Y. Hu, W. Wang, H. Wang and Z.-Y. Bian, Appl. Catal., A, 2016, 522, 145. (complete)

Table 4

63 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 T. Fogeron, P. Retailleau, L.-M. Chamoreau, Y. Li and M. Fontecave, Angew. Chem., Int. Ed., 2018, 57, 17033. (complete)

67 S. Sato and T. Morikawa, ChemPhotoChem, 2018, 2, 207. (complete)

69 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 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.