1H-Nicotinamidium 3,5-dinitrosalicylate

Abstract

Key indicatorsSingle-crystal X-ray study T = 293 K Mean '(C±C) = 0.003 A Ê Disorder in main residue R factor = 0.040 wR factor = 0.110 Data-to-parameter ratio = 9.6For details of how these key indicators were automatically derived from the article, see

Crystal Structures of two Imidazole Derivatives

“…Figures 2 and 3 show the ZORTEP plot of the molecules of BCIC and BCCI with thermal ellipsoids at 30% probability level. The bond lengths and bond angles of the imidazole moiety in BCIC and BCCI are comparable with the standard values [12,13]. The C-C1 distances (C4-C112¼) 1.712(2) Å and 1.723(4) Å are within the range of values reported in the literature [14].…”

Complexation of 5-fluorosalicylic acid with copper(II): A pH-potentiometric, UV–vis spectroscopic, and electron spin resonance study by the two-dimensional simulation of spectra

“…It has been suggested that the active form of ASPIRIN is, in fact, a copper complex formed in vivo [11]. A substantial effort has been devoted to the synthesis and study of solid copper(II)-salicylato complexes in our laboratories as well [12][13][14][15][16][17][18][19], bearing in mind, however, that both the copper(II) ions and the active organic molecules act in the cell, i.e. in 0162-0134/$ -see front matter Ó 2007 Elsevier Inc. All solution.…”

Effect of fluorine position on the coordinating ability of fluorosalicylic acids — An experimental study complemented with computations

“…Moreover, there are inactive ligands that are activated by copper(II) [8]. Synthesis and characterization of solid copper(II)-salicylato complexes have been carried out in our laboratories as well [9][10][11][12][13][14][15][16].…”