Molecule:100787: Difference between revisions

InChI	1S/3C10H8N2.2ClH.Ru/c31-3-7-11-9(5-1)10-6-2-4-8-12-10;;;/h31-8H;2*1H;/q;;;;;+2/p-2
InChI-Key	SJFYGUKHUNLZTK-UHFFFAOYSA-L
SMILES	N12[Ru](Cl)(Cl)3(N4C=CC=CC=4C4C=CC=CN=43)(N3C=CC=CC=3C=1C=CC=C2)1N2C=CC=CC=2C2C=CC=CN=21

Properties
CID	84353
CAS	14323-06-9
IUPAC-Name	2-pyridin-2-ylpyridine;ruthenium(2+);dichloride
Abbreviation	Ru(bpy)3Cl2
Trivialname	Tris(2,2'-bipyridine)ruthenium dichloride
Exact mass	640.048290
Molecular formula	C30H24Cl2N6Ru
LogP	n/a
Has vendors	true
Molecular role	n/a
Synonyms	Tris(2,2'-bipyridine)ruthenium dichloride, ALF8B3WYC2, Tris(2,2'-bipyridyl)ruthenium(II) Chloride, EINECS 238-266-7, NSC 71326, Ruthenium tris(2,2'-bipyridine)-, dichloride, Ruthenium(2+), tris(2,2'-bipyridine)-, dichloride, [[Synonym::Tris[2,2'-bipyridine]ruthenium dichloride]], Tris(2,2'-bipyridine)ruthenium(II) dichloride, Ruthenium(2+), tris(2,2'-bipyridine-.kappa.N1,.kappa.N1')-, dichloride, (OC-6-11)-

Revision as of 10:47, 12 December 2024

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Ru(bpy)3Cl2

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Molecule is used on following pages

topic

publication

Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
Efficient Visible-Light-Driven Carbon Dioxide Reduction using a Bioinspired Nickel Molecular Catalyst
Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH
Pyranopterin Related Dithiolene Molybdenum Complexes as Homogeneous Catalysts for CO2 Photoreduction

investigation

Molecule roles

Investigation type	Photosensitizer
Photocatalytic CO2 conversion experiments	Optimizations of conditions for Co(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2 Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2 Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2 and Ru(bpy)3Cl2 Table 01 Table 1 Table 1 Table 1
Cyclic Voltammetry experiments
Absorption Emission Spectroscopy experiments

@@ Line 11: / Line 11: @@
 |moleculeKey=SJFYGUKHUNLZTK-UHFFFAOYSA-L
 |molOrRxn=
-|smiles=
+  -INDIGO-12122410462D
-|inchi=
+  0  0  0  0  0  0  0  0  0  0 V3000
+M  V30 BEGIN CTAB
+M  V30 COUNTS 39 47 0 0 0
+M  V30 BEGIN ATOM
+M  V30 1 N 1.30208 0.731914 0.0 0
+M  V30 2 C 2.02503 0.334465 0.0 0
+M  V30 3 C 2.73071 0.761834 0.0 0
+M  V30 4 C 2.71343 1.58665 0.0 0
+M  V30 5 C 1.99048 1.9841 0.0 0
+M  V30 6 C 1.28481 1.55673 0.0 0
+M  V30 7 C 2.04231 -0.490355 0.0 0
+M  V30 8 N 1.33663 -0.917725 0.0 0
+M  V30 9 C 1.3539 -1.74254 0.0 0
+M  V30 10 C 2.07685 -2.13999 0.0 0
+M  V30 11 C 2.78253 -1.71262 0.0 0
+M  V30 12 C 2.76526 -0.887804 0.0 0
+M  V30 13 N 0.125472 -1.63593 0.0 0
+M  V30 14 C -0.558829 -2.09676 0.0 0
+M  V30 15 C -0.501895 -2.91979 0.0 0
+M  V30 16 C 0.23934 -3.282 0.0 0
+M  V30 17 C 0.92364 -2.82118 0.0 0
+M  V30 18 C 0.866706 -1.99814 0.0 0
+M  V30 19 C -1.30006 -1.73454 0.0 0
+M  V30 20 N -1.357 -0.911512 0.0 0
+M  V30 21 C -2.09823 -0.549301 0.0 0
+M  V30 22 C -2.78253 -1.01012 0.0 0
+M  V30 23 C -2.7256 -1.83316 0.0 0
+M  V30 24 C -1.98436 -2.19537 0.0 0
+M  V30 25 N -1.22265 0.708208 0.0 0
+M  V30 26 C -1.28359 1.53095 0.0 0
+M  V30 27 C -2.02658 1.88955 0.0 0
+M  V30 28 C -2.70863 1.4254 0.0 0
+M  V30 29 C -2.64769 0.602657 0.0 0
+M  V30 30 C -1.9047 0.24406 0.0 0
+M  V30 31 C -0.601539 1.9951 0.0 0
+M  V30 32 N 0.14145 1.63651 0.0 0
+M  V30 33 C 0.8235 2.10066 0.0 0
+M  V30 34 C 0.762559 2.9234 0.0 0
+M  V30 35 C 0.01957 3.282 0.0 0
+M  V30 36 C -0.662479 2.81785 0.0 0
+M  V30 37 Ru 0.028919 -0.177739 0.0 0
+M  V30 38 Cl 1.08492 -0.111739 0.0 0
+M  V30 39 Cl -0.961081 -0.210738 0.0 0
+M  V30 END ATOM
+M  V30 BEGIN BOND
+M  V30 1 2 1 2
+M  V30 2 1 2 3
+M  V30 3 2 3 4
+M  V30 4 1 4 5
+M  V30 5 2 5 6
+M  V30 6 1 6 1
+M  V30 7 1 2 7
+M  V30 8 2 7 8
+M  V30 9 1 8 9
+M  V30 10 2 9 10
+M  V30 11 1 10 11
+M  V30 12 2 11 12
+M  V30 13 1 12 7
+M  V30 14 2 13 14
+M  V30 15 1 14 15
+M  V30 16 2 15 16
+M  V30 17 1 16 17
+M  V30 18 2 17 18
+M  V30 19 1 18 13
+M  V30 20 1 14 19
+M  V30 21 2 19 20
+M  V30 22 1 20 21
+M  V30 23 2 21 22
+M  V30 24 1 22 23
+M  V30 25 2 23 24
+M  V30 26 1 24 19
+M  V30 27 2 25 26
+M  V30 28 1 26 27
+M  V30 29 2 27 28
+M  V30 30 1 28 29
+M  V30 31 2 29 30
+M  V30 32 1 30 25
+M  V30 33 1 26 31
+M  V30 34 2 31 32
+M  V30 35 1 32 33
+M  V30 36 2 33 34
+M  V30 37 1 34 35
+M  V30 38 2 35 36
+M  V30 39 1 36 31
+M  V30 40 1 37 25 CFG=3
+M  V30 41 1 32 37
+M  V30 42 1 37 20 CFG=1
+M  V30 43 1 37 8 CFG=1
+M  V30 44 1 37 13
+M  V30 45 1 37 1 CFG=3
+M  V30 46 1 39 37
+M  V30 47 1 37 38
+M  V30 END BOND
+M  V30 END CTAB
+M  END
+|smiles=N12[Ru](Cl)(Cl)3(N4C=CC=CC=4C4C=CC=CN=43)(N3C=CC=CC=3C=1C=CC=C2)1N2C=CC=CC=2C2C=CC=CN=21
+|inchi=1S/3C10H8N2.2ClH.Ru/c3*1-3-7-11-9(5-1)10-6-2-4-8-12-10;;;/h3*1-8H;2*1H;/q;;;;;+2/p-2
 |inchikey=SJFYGUKHUNLZTK-UHFFFAOYSA-L
 |width=300px

Molecule:100787: Difference between revisions

Revision as of 10:47, 12 December 2024

Molecule is used on following pages

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Molecule:100787: Difference between revisions

Revision as of 10:47, 12 December 2024

Molecule is used on following pages

Molecule roles

Records for role ""

Current site

Topics