Fig. 2
Characterization of MPC-1 preparations and assessment of catalytic activity. a 1H NMR of MPC-1–2 with peak labels corresponding to proton locations. b Tabulated gel permeation chromatography (GPC) results; PDI = polydispersity index. c GPC chromatograms. d Mark–Houwink plots of MPC-1 preparations. e Scanning electron microscopy (SEM) image of a sheet of MPC-1–2. f High-resolution transmission electron microscopy (HRTEM) images of MPC-1–1 and MPC-1–2. g MPC-1 activity studies: isolated yields of model substrates with MPC-1–1 and MPC-1–2, comparison of MPC-1–2 fractionations in chloroform, and comparison with benchmarking catalysts; PTH = 10-phenylphenothiazine; PDI = N,N-bis(2,6-diisopropylphenyl)perylene-3,4,9,10-bis(dicarboximide). h MPC-1–2 efficacy with hydrodehalogenation of a less reactive substrate and deprotection of a brominated ene-aldehyde. Source data are provided as a Source Data file
