A series of structurally well-defined dinickel carboxylate complexes based on the (BiIBTP)-Bi-R derivatives [(BMITP)-B-R = bis(benzotriazole iminophenolate), where R = 3C for the propylbridged backbone and 5C for the 2,2-dimethy1-1,3-propyl-bridged backbone] were synthesized and developed for copolymerization of CO2, and epoxides. The one-pot reactions of nickel perchlorate with the (R)BilBTP-H-2 proligands and an appropriate amount of carboxylic acid derivatives (CF3COOH or 4-X-C6H4CO2H; X = H, CF3, OMe) upon the addition of triethylamine in refluxing methanol (MeOH) afforded dinuclear nickel dicarboxylate complexes, which could be formulated as either [((BiIBTP)-Bi-R)Ni-2(O2CCF3)(2)] (1 and 2) or [((R)BilBTP)Ni-2(O2CC6H4-4-X)2] (3-7). The dinickel monobenzoate complexes [((R)BilBTP)Ni-2(O2CPh)(ClO4)(H2O)] [R = 3C (8) and 5C (9)] were prepared by using a similar synthetic route in tetrahydrofuran under reflux with a ligand precursor to metal salt to benzoic acid ratio of 1:2:1 in the presence of NEt3. Recrystallization of neutral nickel perchlorate complex 8 in a saturated MeOH or ethanol (EtOH) solution gave ionic and alcohol-solvated monobenzoate bimetallic analogues,[((3C)BilBTP)Ni-2(O2CPh)(S)(2)]ClO4, where S = MeOH (10) and EtOH (11). Single-crystal X-ray crystallography of dinickel analogues 1-11 indicates that the BiLBTP scaffold performs as a N,O,N,N,O,N-hexadentate ligand to chelate two Ni atoms, and the ancillary carboxylate group adopts a bridging bidentate bonding mode. Catalysis for copolymerization of carbon dioxide (CO2) with cyclohexene oxide (CHO) by complexes 1-9 was systematically investigated, and the influence of carboxylate ligands on the catalytic behavior was also studied. Trifluoroacetate-ligated dinickel complex 1 efficiently catalyzed CO2, and CHO with a high turnover frequency (>430 h(-1)) in a controlled fashion, generating perfectly. alternating poly(cyclohexenecarbonate) with large molecular weight (M-n\ > 50000 g/mol). In addition to CO2/CHO copolymerization, bimetallic complex 1 was found to effectively copolymerize CO, with 4-vinyl-1,2-cyclohexene oxide (VCHO) or cyclopentene oxide, producing the high carbonate contents of poly(VCHC-co-VCHO)s and highly alternating poly(cyclopentene carbonate)s, respectively. This study also enabled us to compare the catalytic efficiency of using cyclic epoxides with different ring strains or functional groups as comonomers by the dinickel catalyst 1.