Editing Molecule:100680

{{Molecule
|abbrev=Ru(bpy)3
|trivialname=Tris(2,2'-bipyridyl)ruthenium(II)
|molecular_role=photosensitizer
|cid=65240
|iupacName=2-pyridin-2-ylpyridine;ruthenium(2+)
|molecularMass=570.110585
|molecularFormula=C<sub>30</sub>H<sub>24</sub>N<sub>6</sub>Ru+<sub>2</sub>
|synonyms=Tris(2,2'-bipyridyl)ruthenium(II)$Tris(bipyridine)ruthenium(II)$2-pyridin-2-ylpyridine;ruthenium(2+)$Tris(2,2'-bipyridine)ruthenium II$tris(2,2'-bipyridine)ruthenium(II)$Ru(II)-Tris(bipyridyl)$Ruthenium II tris(2,2'-bipyridine)$tris(2,2/'-bipyridine)ruthenium II$Q27123697$Ruthenium(2+), tris(2,2'-bipyridine-N,N')-, (OC-6-11)-
|cas=15158-62-0
|hasVendors=true
|moleculeKey=HNVRWFFXWFXICS-UHFFFAOYSA-N
|molOrRxn=
  -INDIGO-02142311402D

  0  0  0  0  0  0  0  0  0  0  0 V3000
M  V30 BEGIN CTAB
M  V30 COUNTS 37 45 0 0 0
M  V30 BEGIN ATOM
M  V30 1 N 10.4686 -4.89367 0.0 0
M  V30 2 C 9.86013 -3.35178 0.0 0
M  V30 3 C 9.7559 -4.32845 0.0 0
M  V30 4 C 10.5812 -2.93696 0.0 0
M  V30 5 C 11.2912 -4.28715 0.0 0
M  V30 6 C 11.2672 -3.32813 0.0 0
M  V30 7 C 11.926 -4.59035 0.0 0
M  V30 8 C 13.407 -4.41796 0.0 0
M  V30 9 C 12.6927 -4.07702 0.0 0
M  V30 10 C 13.4744 -5.24515 0.0 0
M  V30 11 N 11.9424 -5.66607 0.0 0
M  V30 12 C 12.7601 -5.88523 0.0 0
M  V30 13 N 12.1907 -7.31984 0.0 0
M  V30 14 C 13.8922 -7.57782 0.0 0
M  V30 15 C 13.0884 -6.97298 0.0 0
M  V30 16 C 13.8688 -8.43063 0.0 0
M  V30 17 C 12.3039 -8.35398 0.0 0
M  V30 18 C 13.1498 -8.81725 0.0 0
M  V30 19 C 11.6693 -8.71536 0.0 0
M  V30 20 C 11.0428 -10.0631 0.0 0
M  V30 21 C 11.7283 -9.63489 0.0 0
M  V30 22 C 10.2824 -9.6709 0.0 0
M  V30 23 N 10.7291 -8.179 0.0 0
M  V30 24 C 10.1211 -8.72059 0.0 0
M  V30 25 C 7.40786 -6.05302 0.0 0
M  V30 26 C 7.41674 -5.26498 0.0 0
M  V30 27 C 8.98334 -5.17125 0.0 0
M  V30 28 C 8.22399 -6.45531 0.0 0
M  V30 29 N 9.14653 -5.94372 0.0 0
M  V30 30 C 8.17252 -7.17954 0.0 0
M  V30 31 C 8.93917 -8.5102 0.0 0
M  V30 32 N 9.12933 -7.59242 0.0 0
M  V30 33 C 8.01894 -8.86654 0.0 0
M  V30 34 C 7.37472 -7.63591 0.0 0
M  V30 35 C 7.32652 -8.42014 0.0 0
M  V30 36 C 8.11795 -4.83872 0.0 0
M  V30 37 Ru 10.613 -6.61608 0.0 0 CHG=2
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 5 7
M  V30 8 2 9 7
M  V30 9 2 10 8
M  V30 10 1 7 11
M  V30 11 1 8 9
M  V30 12 2 11 12
M  V30 13 1 12 10
M  V30 14 2 15 13
M  V30 15 2 16 14
M  V30 16 1 13 17
M  V30 17 1 14 15
M  V30 18 2 17 18
M  V30 19 1 18 16
M  V30 20 1 17 19
M  V30 21 2 21 19
M  V30 22 2 22 20
M  V30 23 1 19 23
M  V30 24 1 20 21
M  V30 25 2 23 24
M  V30 26 1 24 22
M  V30 27 2 26 25
M  V30 28 1 25 28
M  V30 29 2 28 29
M  V30 30 1 29 27
M  V30 31 1 28 30
M  V30 32 2 32 30
M  V30 33 2 33 31
M  V30 34 1 30 34
M  V30 35 1 31 32
M  V30 36 2 34 35
M  V30 37 1 35 33
M  V30 38 2 27 36
M  V30 39 1 36 26
M  V30 40 10 29 37
M  V30 41 10 32 37
M  V30 42 10 23 37
M  V30 43 10 13 37
M  V30 44 10 11 37
M  V30 45 10 1 37
M  V30 END BOND
M  V30 END CTAB
M  END
|smiles=N12[Ru+2](N3=CC=CC=C3C1=CC=CC=2)1(N2C(C3N1=CC=CC=3)=CC=CC=2)1N2C=CC=CC=2C2=N1C=CC=C2
|inchi=1S/3C10H8N2.Ru/c3*1-3-7-11-9(5-1)10-6-2-4-8-12-10;/h3*1-8H;/q;;;+2
|inchikey=HNVRWFFXWFXICS-UHFFFAOYSA-N
|width=300px
|height=200px
|float=none
|logP=
|parent=
}}
Investigation type	Analyte	Photosensitizer
Photocatalytic CO2 conversion experiments		CO2 Reduction under diverse conditions with diverse sensitizers Photocatalytic CO2 reduction: conditions optimization Results Co2+ experiments taken from SI photocatalytic CO2 conversion photocatalytic reduction of CO2 to CO
Cyclic Voltammetry experiments	Dftgsergsfdg
Absorption Emission Spectroscopy experiments
Ultraviolett Visuell experiments
EC conversion of CO2 experiments
EC conversion of CO2 overview experiments