[Synthesis and structure characterization of bis (4-butoxycarbonylaminocyclohexyl) methane].

Bis(4-butoxycarbonylaminocyclohexyl) methane (H12 MDU) was prepared using dicyclohexylmethane-4,4'-diisocyanate and 1-butanol as raw materials and two solid products A and B were obtained. The structures of the two solid products were characterized separately by melting point measurement, infrared spectroscopy, elemental analysis, NMR spectrum analysis and mass spectrum analysis. The results show that both A and B are the target products H12 MDU. The solid A is trans-trans-H12 MDU while the solid B is a mixture including trans-trans-Hiz MDU and at least one of cis-trans-H12MDU and cis-cis-H12 MDU.

[Application of IR spectrum to the research on mechanism of synthesis of 2,4-toluene dicarbamate catalyzed by zinc acetate].

The methoxycarbonylation mechanism of synthesizing 2,4-toluene dicarbamate from 2,4-toluene diamine and dimethyl carbonate catalyzed by anhydrous zinc acetate was investigated by Fourier transform infrared spectroscopy. The result shows that the new coordination complex was formed by oxygen atom of dimethyl carbonate's carbonyl group attaching to zinc atom of anhydrous zinc acetate to form the Zn-O coordination bond, and the anhydrous zinc acetate changed from a bidentate ligand to a unidentate ligand. Simultaneously, dimethyl carbonate's carbonyl group was activated. 2,4-toluene diamine was a nucleophilic reagent, and it's amidos attacked the activated carbon of dimethyl carbonate's carbonyl group in the new coordination complex to produce the methoxycarbonylation compound 2,4-toluene dicarbamate, then the Zn-O coordination bond in the new coordination complex was broken. At the same time, the anhydrous zinc acetate returned to a bidentate ligand.

[Synthesis and crystal structure of a porous coordination polymer [Nd2 (C6H8O4)3 (H2O)2]n x n (4,4'-bpy)].

A novel porous coordination polymer [Nd2 (C6H8O4)3 (H2O)2]n x n (4,4'-bpy) was synthesized by hydrothermal synthesis reaction of hexyl acid, 4,4'-bpy with NdCl3 x XH2O. The structure was characterized by elemental analysis, thermal gravimetric analysis, IR spectroscopy, and X-ray single crystal analysis. The crystal data are of an orthorhombic crystal system, Pbcn space group. Crystallographic data are: a = 2.201 2 nm(6), b = 0.777 8 nm(2), c = 1.972 4 nm(5), alpha = beta = gamma = 90 degrees, V = 337.70 nm(15)3, Z = 4, D(c) = 1.796 g x cm(-3), mu = 3.108 mm(-1), F(000) = 1 800, R = 0.043 0 and wR2 = 0.056 0. X-ray analysis reveals that three-dimensional porous nets were formed between Nd3+ and Nd3+ by carboxyl of hexyl acid.