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Presenter Information

Hannah Arthur, Hollins University

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Event Type

Research Presentation

Academic Department

Chemistry

Start Date

5-4-2021 12:00 AM

Description

Two analogs of the compound dppm (Ph2PCH2PPh2) were synthesized: dppmCN (Ph2PCH(CN)PPh2) and dppmMe (Ph2PCH(CH3)PPh2). These diphosphines were subsequently used to prepare complexes of the type Re2(O2CCH3)Cl4(dppmR)2 (R = CN, CH3). The dirhenium starting material for these reactions was Re2(O2CCH3)2Cl4(H2O)2, which was prepared from commercially available (n-Bu4N)2Re2Cl8. All compounds were characterized by infrared spectroscopy. The dirhenium compounds were further characterized by cyclic voltammetry. The ultimate goal of this project is to make species of the type Re2(O2CCH3)2Cl2(dppmR)2. If we successfully prepare the cis isomer of Re2(O2CCH3)2Cl2(dppmR)2, the absence of one of the two bridgehead hydrogens in each of two dppm ligands of cis-Re2(O2CCH3)2Cl2(dppm)2 may help us to understand the reason for the unusual chemical shift of one of the –CH2– hydrogens in the H-1 nuclear magnetic resonance spectrum of the dirhenium compound that contains dppm.

Comments

Under the direction of Dr. Dan Derringer.

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Apr 5th, 12:00 AM

Two diphosphines and the dirhenium compounds derived from them

Two analogs of the compound dppm (Ph2PCH2PPh2) were synthesized: dppmCN (Ph2PCH(CN)PPh2) and dppmMe (Ph2PCH(CH3)PPh2). These diphosphines were subsequently used to prepare complexes of the type Re2(O2CCH3)Cl4(dppmR)2 (R = CN, CH3). The dirhenium starting material for these reactions was Re2(O2CCH3)2Cl4(H2O)2, which was prepared from commercially available (n-Bu4N)2Re2Cl8. All compounds were characterized by infrared spectroscopy. The dirhenium compounds were further characterized by cyclic voltammetry. The ultimate goal of this project is to make species of the type Re2(O2CCH3)2Cl2(dppmR)2. If we successfully prepare the cis isomer of Re2(O2CCH3)2Cl2(dppmR)2, the absence of one of the two bridgehead hydrogens in each of two dppm ligands of cis-Re2(O2CCH3)2Cl2(dppm)2 may help us to understand the reason for the unusual chemical shift of one of the –CH2– hydrogens in the H-1 nuclear magnetic resonance spectrum of the dirhenium compound that contains dppm.