Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH: Difference between revisions

Revision as of 16:07, 13 February 2023

Investigations

Table 1 (Molecular process, Photocatalytic CO2 conversion experiments)

DOI	10.1016/j.electacta.2017.04.080
Authors	Matthew Stanbury, Jean-Daniel Compain, Monica Trejo, Parker Smith, Eric Gouré, Sylvie Chardon-Noblat,
Submitted	18.04.2017
Licenses	https://www.elsevier.com/tdm/userlicense/1.0/,
Subjects	Electrochemistry, General Chemical Engineering
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 [[Category:Photocatalytic CO2 conversion to HCOOH]]
 {{BaseTemplate}}
+<chemform smiles="C1C=CN2[Mn+]([Br-])(C#O)(C#O)(C#O)N3=CC=CC4C(=O)C(=O)C=1C=2C=43" inchi="1S/C12H6N2O2.3CHO.BrH.Mn/c15-11-7-3-1-5-13-9(7)10-8(12(11)16)4-2-6-14-10;3*1-2;;/h1-6H;3*1H;1H;/q;;;;;+1/p-1" inchikey="ZMUYZQUZOJZTSM-UHFFFAOYSA-M" height="200px" width="300px" float="none">
+  -INDIGO-02132316042D
+  0  0  0  0  0  0  0  0  0  0 V3000
+M  V30 BEGIN CTAB
+M  V30 COUNTS 24 27 0 0 0
+M  V30 BEGIN ATOM
+M  V30 1 C 6.40083 -3.01814 0.0 0
+M  V30 2 C 7.89956 -3.88287 0.0 0
+M  V30 3 C 7.40155 -3.01842 0.0 0
+M  V30 4 N 7.39909 -4.74971 0.0 0
+M  V30 5 C 5.89836 -3.88844 0.0 0
+M  V30 6 C 6.40341 -4.75162 0.0 0
+M  V30 7 C 7.90019 -2.15789 0.0 0
+M  V30 8 C 8.89805 -2.15853 0.0 0
+M  V30 9 C 8.90142 -3.88351 0.0 0
+M  V30 10 C 9.39546 -3.01753 0.0 0
+M  V30 11 C 10.3894 -3.01305 0.0 0
+M  V30 12 C 10.8927 -3.87395 0.0 0
+M  V30 13 N 9.40673 -4.74785 0.0 0
+M  V30 14 C 10.403 -4.73667 0.0 0
+M  V30 15 O 7.40019 -1.29186 0.0 0
+M  V30 16 O 9.39805 -1.2925 0.0 0
+M  V30 17 Mn 8.375 -5.525 0.0 0 CHG=1
+M  V30 18 C 7.50897 -6.025 0.0 0
+M  V30 19 C 9.24102 -6.025 0.0 0
+M  V30 20 C 8.375 -6.525 0.0 0
+M  V30 21 Br 8.375 -4.525 0.0 0 CHG=-1
+M  V30 22 O 6.64295 -6.525 0.0 0
+M  V30 23 O 8.375 -7.525 0.0 0
+M  V30 24 O 10.1071 -6.525 0.0 0
+M  V30 END ATOM
+M  V30 BEGIN BOND
+M  V30 1 2 3 1
+M  V30 2 2 4 2
+M  V30 3 1 1 5
+M  V30 4 1 2 3
+M  V30 5 2 5 6
+M  V30 6 1 6 4
+M  V30 7 1 8 7
+M  V30 8 1 2 9
+M  V30 9 1 7 3
+M  V30 10 2 9 10
+M  V30 11 1 10 8
+M  V30 12 2 12 11
+M  V30 13 1 9 13
+M  V30 14 1 11 10
+M  V30 15 2 13 14
+M  V30 16 1 14 12
+M  V30 17 2 7 15
+M  V30 18 2 8 16
+M  V30 19 10 4 17
+M  V30 20 10 13 17
+M  V30 21 10 17 18
+M  V30 22 10 17 19
+M  V30 23 10 17 20
+M  V30 24 10 17 21
+M  V30 25 3 18 22
+M  V30 26 3 20 23
+M  V30 27 3 19 24
+M  V30 END BOND
+M  V30 END CTAB
+M  END
+</chemform><chemform smiles="C12N3[Mn+](C#O)(C#O)(C#O)(N#CC)N4=CC=CC(C(=O)C(=O)C=1C=CC=3)=C24" inchi="1S/C12H6N2O2.C2H3N.3CHO.Mn/c15-11-7-3-1-5-13-9(7)10-8(12(11)16)4-2-6-14-10;1-2-3;3*1-2;/h1-6H;1H3;3*1H;/q;;;;;+1" inchikey="YEWOWPOKKZXMQA-UHFFFAOYSA-N" height="200px" width="300px" float="none">
+  -INDIGO-02132316072D
+  0  0  0  0  0  0  0  0  0  0 V3000
+M  V30 BEGIN CTAB
+M  V30 COUNTS 26 29 0 0 0
+M  V30 BEGIN ATOM
+M  V30 1 C 8.22511 -3.34193 0.0 0
+M  V30 2 C 8.22463 -1.61163 0.0 0
+M  V30 3 C 7.72501 -2.47514 0.0 0
+M  V30 4 C 9.22557 -1.61163 0.0 0
+M  V30 5 C 9.23006 -3.34193 0.0 0
+M  V30 6 C 9.72507 -2.47296 0.0 0
+M  V30 7 N 7.72549 -4.20544 0.0 0
+M  V30 8 C 6.72455 -4.20544 0.0 0
+M  V30 9 C 6.72006 -2.47514 0.0 0
+M  V30 10 C 6.22505 -3.34411 0.0 0
+M  V30 11 C 10.7221 -2.46783 0.0 0
+M  V30 12 C 11.2275 -3.33106 0.0 0
+M  V30 13 N 9.73749 -4.20861 0.0 0
+M  V30 14 C 10.7369 -4.19675 0.0 0
+M  V30 15 O 7.72503 -0.74537 0.0 0
+M  V30 16 O 9.72474 -0.745122 0.0 0
+M  V30 17 Mn 8.75 -4.975 0.0 0 CHG=1
+M  V30 18 N 10.8 -4.975 0.0 0
+M  V30 19 C 7.76789 -5.55711 0.0 0
+M  V30 20 C 9.78211 -5.53211 0.0 0
+M  V30 21 C 8.75 -5.975 0.0 0
+M  V30 22 O 6.90187 -6.05711 0.0 0
+M  V30 23 O 8.75 -6.975 0.0 0
+M  V30 24 O 10.6481 -6.03211 0.0 0
+M  V30 25 C 11.5909 -4.96618 0.0 0
+M  V30 26 C 12.3319 -4.95736 0.0 0
+M  V30 END ATOM
+M  V30 BEGIN BOND
+M  V30 1 2 3 1
+M  V30 2 1 4 2
+M  V30 3 1 1 5
+M  V30 4 1 2 3
+M  V30 5 2 5 6
+M  V30 6 1 6 4
+M  V30 7 2 8 7
+M  V30 8 1 3 9
+M  V30 9 1 7 1
+M  V30 10 2 9 10
+M  V30 11 1 10 8
+M  V30 12 2 12 11
+M  V30 13 1 5 13
+M  V30 14 1 11 6
+M  V30 15 2 13 14
+M  V30 16 1 14 12
+M  V30 17 2 2 15
+M  V30 18 2 4 16
+M  V30 19 10 7 17
+M  V30 20 10 17 13
+M  V30 21 10 17 18
+M  V30 22 10 17 19
+M  V30 23 10 17 20
+M  V30 24 10 17 21
+M  V30 25 3 19 22
+M  V30 26 3 21 23
+M  V30 27 3 20 24
+M  V30 28 3 18 25
+M  V30 29 1 25 26
+M  V30 END BOND
+M  V30 END CTAB
+M  END
+</chemform>

Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH: Difference between revisions

Revision as of 16:07, 13 February 2023

Investigations

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