“…For example, the BrÀBr ionic-ionic contacts between the PBr 4 + and Br À ions in PBr 5 or between the PBr 4 + and Br 3 À ions in PBr 7 . [18] Note that this value is very close to the intermolecular contacts between dibromine molecules in solid Br 2 (3.30 ). [19] In…”
The double salts Rb(3)[Mo(6)Br(i) (7)Y(i)Br(a) (6)](Rb(3)[MoBr(6)])(3) (Y=Se, Te) result from the partial disproportionation of the Mo(6)Br(12) octahedral-cluster-based bromide, in the presence of corresponding chalcogenides and RbBr salt (crystal data: Rb(12)[MoBr(6)](3)[Mo(6)Br(i) (7)Te(i)Br(a) (6)] (1), Pm$\bar 3$m (No. 221), a=12.1558(2) A, Z=1, R(1)=0.028; wR(2)=0.050; Rb(12)[MoBr(6)](3)[Mo(6)Br(i) (7)Se(i)Br(a) (6)] (2), Pm$\bar 3$m, a=12.144(3) A, Z=1, R(1)=0.028; wR(2)=0.050). The structures of 1 and 2 are built up from [Mo(III)Br(6)](3-) complexes and [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) cluster units characterised by a random distribution of seven bromine and one chalcogen ligands on all the eight inner positions that face cap the Mo(6) clusters. Such a distribution implies a static orientational disorder of the [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) units around the origin of the unit cell. Close-packed anionic layers based on [Mo(III)Br(6)](3-) complexes and [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) cluster units are stacked in the sequence ABC. This arrangement leads to very short Br(a)--Br(a) intercluster unit distances of 3.252 A, much lower than the sum of the van der Waals radii (3.70 A). The trivalent oxidation state of molybdenum in the Mo complexes and 24 valence electrons per Mo(6) cluster have been confirmed by magnetic susceptibility measurements. Salts 1 and 2 constitute the first examples of structurally characterised bromides containing discrete [Mo(III)Br(6)](3-) complexes obtained by means of solid-state synthesis.
“…For example, the BrÀBr ionic-ionic contacts between the PBr 4 + and Br À ions in PBr 5 or between the PBr 4 + and Br 3 À ions in PBr 7 . [18] Note that this value is very close to the intermolecular contacts between dibromine molecules in solid Br 2 (3.30 ). [19] In…”
The double salts Rb(3)[Mo(6)Br(i) (7)Y(i)Br(a) (6)](Rb(3)[MoBr(6)])(3) (Y=Se, Te) result from the partial disproportionation of the Mo(6)Br(12) octahedral-cluster-based bromide, in the presence of corresponding chalcogenides and RbBr salt (crystal data: Rb(12)[MoBr(6)](3)[Mo(6)Br(i) (7)Te(i)Br(a) (6)] (1), Pm$\bar 3$m (No. 221), a=12.1558(2) A, Z=1, R(1)=0.028; wR(2)=0.050; Rb(12)[MoBr(6)](3)[Mo(6)Br(i) (7)Se(i)Br(a) (6)] (2), Pm$\bar 3$m, a=12.144(3) A, Z=1, R(1)=0.028; wR(2)=0.050). The structures of 1 and 2 are built up from [Mo(III)Br(6)](3-) complexes and [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) cluster units characterised by a random distribution of seven bromine and one chalcogen ligands on all the eight inner positions that face cap the Mo(6) clusters. Such a distribution implies a static orientational disorder of the [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) units around the origin of the unit cell. Close-packed anionic layers based on [Mo(III)Br(6)](3-) complexes and [Mo(6)Br(i) (7)Y(i)Br(a) (6)](3-) cluster units are stacked in the sequence ABC. This arrangement leads to very short Br(a)--Br(a) intercluster unit distances of 3.252 A, much lower than the sum of the van der Waals radii (3.70 A). The trivalent oxidation state of molybdenum in the Mo complexes and 24 valence electrons per Mo(6) cluster have been confirmed by magnetic susceptibility measurements. Salts 1 and 2 constitute the first examples of structurally characterised bromides containing discrete [Mo(III)Br(6)](3-) complexes obtained by means of solid-state synthesis.
“…Among these, the polybromide anions have shown the largest variety. Especially our knowledge about dianions was vastly expanded due to the structures of [ [3,4] or of polybromide networks [3, 5 -7] 3 ] − has been fully characterized, including the single-crystal structure of one of its salts [1,8,9]. Beyond this, no structural data of a higher polybromide monoanion was known prior to our reports in recent years.…”
[HMIM] [Br 9 ] ([HMIM] = 1-hexyl-3-methylimidazolium) has been investigated by Raman spectroscopy, single-crystal X-ray diffraction and NMR spectroscopy. Conductivity measurements show a high electrical conductivity like other polybromides.
“…Structural studies of the tribromide ion previously done have shown that Br~-in [(CH3)3NH÷]zBr-Br~ (Romers & Keulemans, 1958) is an essentially symmetrical ion with the two bond lengths almost equal while Br~-in PBr7 (Breneman & Willett, 1967) is extremely distorted from the symmetrical configuration with the two bond lengths differing by more than 0.5 •. Both of these Br~-ions are essentially linear.…”
The crystal structure of CsBr3 has been determined by X-ray diffraction techniques. The unit cell is orthorhombic with a=6.52, b=10.04 and c=9"54A. The space group is Pmnb. The tribromide ion is nearly linear, but unsymmetrical, with Br-Br distances of 2.440 and 2.698 A,. The Br7 ions in this compound, in PBr7, and in [(CH3)3NH+]2Br-Br7 form a system analogous to that of 17 in which the configuration of the trihalide ion depends on the cation present in the crystal. A qualitative discussion comparing the two systems is given.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.