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Substrate-Selective Catalysis and CCC-Pincer Ligands Anthony R. Chianese, Department of Chemistry, Colgate University Sendritic, bowl-shaped N-heterocyclic carbene ligands G0-G2 were synthesized to demonstrate substrate specificity based on size and shape in iridium-catalyzed ketone hydrosilylation: Ligand 0 0.5 1 1.5 2 2.5 3 3.5 4 11a vs.11b 11a vs.11c 11a vs.11d R elative InitialR ates G0 G1 G2 Substrate Specificity G2 G1 G0 Aryl-substituted CCC-pincer ligands were synthesized, and metalation to iridium gives solvated hydridochloride complexes that may be useful for homogeneous catalysis, including C-H functionalization and hydroamination X-ray structure: Ar = mesityl

Substrate-Selective Catalysis and CCC-Pincer Ligands

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Substrate-Selective Catalysis and CCC-Pincer LigandsAnthony R. Chianese, Department of Chemistry, Colgate University

Sendritic, bowl-shaped N-heterocyclic carbene ligands G0-G2 were synthesized to demonstrate substrate specificity based on size and shape in

iridium-catalyzed ketone hydrosilylation:

Ligand

0

0.5

1

1.5

2

2.5

3

3.5

4

11a vs. 11b 11a vs. 11c 11a vs. 11d

Rel

ativ

e In

itia

l Rat

es

G0

G1

G2

Substrate Specificity

G2

G1

G0

Aryl-substituted CCC-pincer ligands were synthesized, and metalation to iridium gives solvated

hydridochloride complexes that may be useful for homogeneous catalysis, including C-H functionalization and hydroamination

X-ray structure: Ar = mesityl