crystal structure, thermal analysis and ir spectroscopic investigation of bis (n-methyl anilinium) sulfate晶体结构、热分析和红外光谱对bis(n-methyl anilinium)硫酸.pdfVIP

crystal structure, thermal analysis and ir spectroscopic investigation of bis (n-methyl anilinium) sulfate晶体结构、热分析和红外光谱对bis(n-methyl anilinium)硫酸.pdf

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crystal structure, thermal analysis and ir spectroscopic investigation of bis (n-methyl anilinium) sulfate晶体结构、热分析和红外光谱对bis(n-methyl anilinium)硫酸

Open Journal of Inorganic Chemistry, 2011, 1, 47-53 OJIC doi:10.4236/ojic.2011.13007 Published Online October 2011 (http://www.SciRP.org/journal/ojic/). Crystal structure, thermal analysis and IR spectroscopic investigation of bis (N-methyl anilinium) sulfate * Taha Guerfel , Amor Jouini Laboratoire de Chimie du Solide, Faculté des Sciences de Monastir, Monastir, Tunisie. Email: taha_guerfel@yahoo.fr Received 10 August 2011; revised 20 September 2011; accepted 10 October 2011. ABSTRACT influencing the dimensions of sulfate anion–organic ca- tion interaction. We report here the chemical preparation, Chemical preparation, X-ray single crystal, thermal crystallographic features, thermal behavior, and IR ana- analysis and IR spectroscopic investigation of (C7H10 lysis of a new organic sulfate, (C H N) ·SO . 7 10 2 4 N)2·SO4 denoted NMAS are described. The NMAS 2. EXPERIMENT crystallizes in the triclinic system with P-1 space group. Its unit cell dimensions are a = 9.6150(5) Å, b 2.1. Chemical Preparation = 9.9744(3) Å, c = 10.2767(6) Å,  = 68.069(3),  = 62.929(2),  = 67.285(3) with V = 785.72(7) Å3 and Z = Crystals of NMAS were prepared by slow evaporation at 2. The structure has been solved using direct me- room temperature of 400 mL of an aqueous solution of thod and refined to a reliability R factor of 3.62%. H2SO4 (10–1 M), neutralized by 0.0

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