Editing Molecule:100651

{{Molecule
|abbrev=Eosin Y
|trivialname=Eosin
|cid=11048
|iupacName=disodium;2-[2,4,5,7-tetrakis(bromanyl)-3-oxidanidyl-6-oxidanylidene-xanthen-9-yl]benzoate
|molecularMass=691.67031
|molecularFormula=C<sub>20</sub>H<sub>6</sub>Br<sub>4</sub>Na<sub>2</sub>O<sub>5</sub>
|synonyms=Eosin$Eosin yellowish$Eosine Yellowish$Eosine$C.I. Acid Red 87$Eosine G$Eosin YS$Bromoeosine$Sodium eosine$Bromo acid
|cas=548-26-5
|hasVendors=true
|moleculeKey=SEACYXSIPDVVMV-UHFFFAOYSA-L
|molOrRxn=
  -INDIGO-11282310442D

  0  0  0  0  0  0  0  0  0  0  0 V3000
M  V30 BEGIN CTAB
M  V30 COUNTS 31 32 0 0 0
M  V30 BEGIN ATOM
M  V30 1 C 5.20985 -5.97507 0.0 0
M  V30 2 C 6.94015 -5.97459 0.0 0
M  V30 3 C 6.07664 -5.47497 0.0 0
M  V30 4 C 6.94015 -6.97553 0.0 0
M  V30 5 C 5.20985 -6.98002 0.0 0
M  V30 6 C 6.07882 -7.47503 0.0 0
M  V30 7 C 7.80465 -5.47621 0.0 0
M  V30 8 C 8.67183 -5.97655 0.0 0
M  V30 9 O 7.8108 -7.47787 0.0 0
M  V30 10 C 8.67403 -6.97246 0.0 0
M  V30 11 C 9.53088 -5.47878 0.0 0
M  V30 12 C 10.3948 -5.97469 0.0 0
M  V30 13 C 9.54141 -7.47035 0.0 0
M  V30 14 C 10.3992 -6.96559 0.0 0
M  V30 15 C 7.80482 -4.47621 0.0 0
M  V30 16 C 6.93825 -2.97855 0.0 0
M  V30 17 C 6.93799 -3.97619 0.0 0
M  V30 18 C 7.80475 -2.4775 0.0 0
M  V30 19 C 8.6748 -3.97316 0.0 0
M  V30 20 C 8.66833 -2.9731 0.0 0
M  V30 21 Br 11.2591 -5.47169 0.0 0
M  V30 22 O 11.2684 -7.46007 0.0 0
M  V30 23 Br 9.54681 -8.47034 0.0 0
M  V30 24 Br 6.08268 -8.47503 0.0 0
M  V30 25 O 4.34528 -7.48253 0.0 0 CHG=-1
M  V30 26 Br 4.3439 -5.47495 0.0 0
M  V30 27 C 9.5426 -4.47007 0.0 0
M  V30 28 O 9.5426 -3.47007 0.0 0 CHG=-1
M  V30 29 O 10.4586 -4.09507 0.0 0
M  V30 30 Na 10.375 -2.925 0.0 0 CHG=1
M  V30 31 Na 3.975 -8.2 0.0 0 CHG=1
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 2 8 7
M  V30 8 1 4 9
M  V30 9 1 7 2
M  V30 10 1 9 10
M  V30 11 1 10 8
M  V30 12 2 12 11
M  V30 13 2 10 13
M  V30 14 1 11 8
M  V30 15 1 13 14
M  V30 16 1 14 12
M  V30 17 1 7 15
M  V30 18 2 17 15
M  V30 19 2 18 16
M  V30 20 1 15 19
M  V30 21 1 16 17
M  V30 22 2 19 20
M  V30 23 1 20 18
M  V30 24 1 12 21
M  V30 25 2 14 22
M  V30 26 1 13 23
M  V30 27 1 6 24
M  V30 28 1 5 25
M  V30 29 1 1 26
M  V30 30 1 19 27
M  V30 31 1 27 28
M  V30 32 2 27 29
M  V30 END BOND
M  V30 END CTAB
M  END
|smiles=C(Br)1C([O-])=C(Br)C2OC3=C(Br)C(=O)C(Br)=CC3=C(C3C(C(=O)[O-])=CC=CC=3)C=2C=1.[Na+].[Na+]
|inchi=1S/C20H8Br4O5.2Na/c21-11-5-9-13(7-3-1-2-4-8(7)20(27)28)10-6-12(22)17(26)15(24)19(10)29-18(9)14(23)16(11)25;;/h1-6,25H,(H,27,28);;/q;2*+1/p-2
|inchikey=SEACYXSIPDVVMV-UHFFFAOYSA-L
|width=300px
|height=200px
|float=none
|logP=
|parent=
}}
Investigation type	Catalyst	Photosensitizer
Photocatalytic CO2 conversion experiments	inv0	Table 1 photocatalytic reduction of CO2 to CO
Cyclic Voltammetry experiments
Absorption Emission Spectroscopy experiments
Ultraviolett Visuell experiments
EC conversion of CO2 experiments
EC conversion of CO2 overview experiments
Host Guest interaction experiments