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. 2023 Oct 23;13(44):30978–30984. doi: 10.1039/d3ra05971e

Polymerization results of chiral phenylacetylenes (3R and 3S) with a Rh-based multicomponent catalyst system using initiator Aa.

Run Monomer [3]/([A]/3) Polymer
Sample code Yieldb (%) M n × 10−4c M w/Mnc
6 3R 25 A(poly-3R25)3 95 2.0 1.02
7 3S 25 A(poly-3S25)3 90 2.1 1.03
8 3R 500 A(poly-3R500)3 83 33.4 1.48
9 3S 500 A(poly-3S500)3 80 32.7 1.60
a

Reaction conditions: A (0.10 mmol), [Rh(nbd)Cl]2 (0.067 mmol), DPA (0.2 mmol), in THF (0.2 mL) at 0 °C for 10 min, then phenylacetylene (1) (0.85 mmol (runs 6 and 7), 17.0 mmol (runs 8 and 9)) and PPh3 (0.2 mmol) in THF (3.8 mL) at 30 °C for 1 h.

b

Methanol-insoluble part.

c

Determined by SEC using three columns (TSKgel G4000HXL + G3000HXL + G3000HXL) connected in series (runs 6 and 7) or one column (KF-805L) (runs 8 and 9) based on polystyrene standards (THF, 40 °C).