Molecule:100662: Difference between revisions

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molecule
auto-generated
auto-generated
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{{Molecule
{{Molecule
|abbrev=[NBu4]2[MoO(qpdt)2]
|abbrev=[NBu4]2[MoO(qpdt)2]
|molecularFormula=C<sub>58</sub>H<sub>96</sub>MoN<sub>6</sub>O<sub>3</sub>S<sub>4</sub>
|molecularFormula=C<sub>60</sub>H<sub>104</sub>MoN<sub>6</sub>O<sub>3</sub>S<sub>4</sub>
|moleculeKey=SZEIOHNZAHLTPQ-UHFFFAOYSA-J
|moleculeKey=SZEIOHNZAHLTPQ-UHFFFAOYSA-J
|molOrRxn=
|molOrRxn=
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M  V30 END CTAB
M  V30 END CTAB
M  END
M  END
|smiles=[Mo-2](=O)1(~SC2C3=NC4C=CC=CC=4N(C)C3OC(C)(C)C=2S~1)1~SC2C(C)(C)OC3N(C)C4C=CC=CC=4N=C3C=2S~1.[N+](CCCC)(CCCC)(CCCC)CCCC.[N+](CCCC)(CCCC)(CCCC)CCCC
|smiles=[Mo-2](=O)1(~SC2C3=NC4C=CC=CC=4N(C)C3OC(C)(C)C=2S~1)1~SC2C(C)(C)OC3N(C)C4C=CC=CC=4N=C3C=2S~1.[N+](CCCC)(CCCC)(CCCC)CCCC.[N+](CCCC)(CCCC)(CCCC)CCCC
|inchi=1S/2C16H36N.2C14H16N2OS2.Mo.O/c2*1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;2*1-14(2)12(19)11(18)10-13(17-14)16(3)9-7-5-4-6-8(9)15-10;;/h2*5-16H2,1-4H3;2*4-7,13,18-19H,1-3H3;;/q2*+1;;;+2;/p-4
|inchi=1S/2C16H36N.2C14H16N2OS2.Mo.O/c2*1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;2*1-14(2)12(19)11(18)10-13(17-14)16(3)9-7-5-4-6-8(9)15-10;;/h2*5-16H2,1-4H3;2*4-7,13,18-19H,1-3H3;;/q2*+1;;;+2;/p-4
|inchikey=SZEIOHNZAHLTPQ-UHFFFAOYSA-J
|inchikey=SZEIOHNZAHLTPQ-UHFFFAOYSA-J
|width=300px
|width=200
|height=200px
|height=200
|float=none
|float=none
|molecularMass=1150.548083132
|molecularMass=1182.610683388
|trivialname=
|trivialname=
|synonyms=
|synonyms=

Revision as of 15:28, 10 January 2024

Properties
CID n/a
CAS n/a
IUPAC-Name n/a
Abbreviation [NBu4]2[MoO(qpdt)2]
Trivialname n/a
Exact mass 1182.610683388
Molecular formula C60H104MoN6O3S4
LogP n/a
Has vendors n/a
Molecular role n/a
Synonyms n/a

[MoO(qpdt)2][NBu4]2


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Molecule is used on following pages

topic
publication
investigation

Molecule roles

Investigation type Catalyst
Photocatalytic CO2 conversion experiments
Cyclic Voltammetry experiments
Absorption Emission Spectroscopy experiments
Ultraviolett Visuell experiments