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Tris[5-fluoro-2-(2-pyridinyl-kN)phenyl-kC]iridium(III), 95%

Catalog Number
ACM370878696
Product Name
Tris[5-fluoro-2-(2-pyridinyl-kN)phenyl-kC]iridium(III), 95%
CAS
370878-69-6
  • Product Overview
  • Usage
Synonyms
Ir(p-F-ppy)3;370878-69-6;AK00767414;
IUPAC Name
2-(4-fluorobenzene-6-id-1-yl)pyridine;iridium(3+);
Molecular Weight
708.764g/mol
Molecular Formula
C33H21F3IrN3;
Canonical SMILES
C1=CC=NC(=C1)C2=CC=C(C=[C-]2)F.C1=CC=NC(=C1)C2=CC=C(C=[C-]2)F.C1=CC=NC(=C1)C2=CC=C(C=[C-]2)F.[Ir+3];
InChI
InChI=1S/3C11H7FN.Ir/c3*12-10-6-4-9(5-7-10)11-3-1-2-8-13-11;/h3*1-4,6-8H;/q3*-1;+3;
InChI Key
ZEBLNIAOTYJLBU-UHFFFAOYSA-N;
Complexity
972
Covalently-Bonded Unit Count
4
Exact Mass
709.132g/mol
H-Bond Acceptor
9
Heavy Atom Count
40
Monoisotopic Mass
709.132g/mol
Topological Polar Surface Area
38.7A^2
Application
Tris[5-fluoro-2-(2-pyridinyl-kN)phenyl-kC]iridium(III), 95%, serves as a versatile photocatalyst designed to drive a variety of chemical transformations under visible light. Its applications include facilitating the decarboxylative arylation of α-amino acids, enabling the enantioselective coupling of (N-arylamino)methanes with (Nmethanesulfonyl)-aldimines in the presence of a P-Spiro chiral (arylamino)phosphonium catalyst, and promoting [2+2] styrene cycloadditions. Furthermore, this compound efficiently catalyzes the azoylation of trimethoxybenzene via C-H functionalization, showcasing its broad utility in complex organic syntheses.
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