Abstract
A series of metal−organic gels (MOGs) were formed in CH3OH−CHCl3 solution based on L1 and Pd(COD)(NO3)2 (L1 = 4,4′,4′′-(1,3,5-triazine-2,4,6-triyl)tris(N-(pyridin-3-ylmethyl)benzamide, COD = cycloocta-1,5-diene) at different ratios. FT-IR, NMR, and fluorescence spectroscopy show that hydrogen bonding, π−π interaction, and coordination bonding are involved in the gel formation. The morphologies of these metallogels are Pd/L1 ratio dependent ranging from spheres to fibers. The fibrous networked gel shows higher catalytic activity in Suzuki−Miyaura coupling reaction than the spherical gel, acting as recyclable Pd(II) catalyst supported by the air-stable networked gel/xerogel.
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