Electric Literature of C5H10Br2. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: 1,5-Dibromopentane, is researched, Molecular C5H10Br2, CAS is 111-24-0, about Hybrid bromobismuthates: Synthesis, thermal stability and crystal structure of multicharged 3-ammoniopyridinium derivatives. Author is Kotov, Vitalii Yu.; Buikin, Petr A.; Simonenko, Nikolay P.; Ilyukhin, Andrey B..
Five new derivatives of 3-ammoniopyridine, namely, 1,1′-(1,4-phenylenebis(methylene))bis (3-ammoniopyridinium) bromobismuthate-bromide [(3-NH3Py)2XK][BiBr6]Br·H2O (1), 3-amino-1-(3-(3-ammoniopyridin-1-ium-1-yl)propyl)pyridin-1-ium bromobismuthate [(3-NH2Py)(3-NH3Py)C3][BiBr6]·1.5H2O (2), 1,1′-(butane-1,1′-diyl)bis(3-ammoniopyridinium) bromobismuthate [(3-NH3Py)2C4][Bi2Br10] (3) and bromide [(3-NH3Py)2C4]Br4·2H2O (4), and 3-amino-1-(5-(3-ammoniopyridin-1-ium-1-yl)pentyl)pyridin-1-ium bromobismuthate [(3-NH2Py)(3-NH3Py)C5][BiBr6]·H2O (5), were successfully obtained from concentrated HBr solutions and characterized by single crystal X-Ray diffraction, XRD, DRS, and TG/DTA methods. All compounds are unstable and decompose slowly in humid air. According to DFT calculations the protonation of the amino group results in the increase of the electron affinity of the organic cation and leads to changes in the structure of the aminopyridine fragment of the cation. The C-NHn bond length values in 3-aminopyridinium (<1.40 Å) and in 3-ammoniopyridinium (≥1.44 Å) derivatives allows to uniquely determine the protonation degree of the N atom. From this literature《Hybrid bromobismuthates: Synthesis, thermal stability and crystal structure of multicharged 3-ammoniopyridinium derivatives》,we know some information about this compound(111-24-0)Electric Literature of C5H10Br2, but this is not all information, there are many literatures related to this compound(111-24-0).
Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis