2-Aminopyridinium maleate: A structural study
β Scribed by R. Chitra; Pascal Roussel; Fredric Capet; Chitra Murli; R.R. Choudhury
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 550 KB
- Volume
- 891
- Category
- Article
- ISSN
- 0022-2860
No coin nor oath required. For personal study only.
β¦ Synopsis
A new complex of 2-aminopyridine and maleate in 1:1 stoichiometric ratio was obtained. The complex crystallizes in non-centrosymmetric space group Pc. This complex is held by network of hydrogen bonding between the protonated 2-aminopyridinium cation and maleate anion and also by pi-pi stacking. There is no phase transition observed in this complex, which has been verified using DSC and single crystal X-ray measurement studies. A comparison between 2-aminopyridinium maleate and bis(2-aminopyridinium) maleate structure shows that the positive charge resides on the ring nitrogen in the present complex unlike the case in bis(2-aminopyridinium) maleate where the charge is on the amino nitrogen. This complex has higher meting point compared to that of bis(2-aminopyridinium) maleate which is due to the difference in hydrogen bonding pattern between the two complexes.
π SIMILAR VOLUMES
A novel organic nonlinear optical material bis(2-aminopyridinium) maleate (B2AM) was synthesized and crystals were grown from aqueous solution. The solubility and metastable zone width were determined. Single crystal X-ray diffraction and Fourier transform infrared spectral analysis were carried out
ESR study of 1% Cu \*+ doped m zmc maleate tetrahydrate smgle crystal gives rise to g1 = 2 374, g2 = 2 257 and i, = 2 643 These ialues are quite different from the g values for the pure copper comnound Conner maleate tetrahvdrate. w (111 = 2 172 and gI = 2 095, mdlcatmg that m Cu'+/ZnMTH, Cu" occup&