Bromoantimonates are compounds containing anions composed of bromide (Br−) and antimony (Sb). They can be considered as double bromides, metallohalides or halometallates. They are in the category of halopnictates. Related compounds include the bromobismuthates, iodoantimonates, bromophosphates, and bromoarsenates.
Some examples of bromoantimonates
Bromoantimonates can have antimony in one of two oxidation states, either +3 or +5. These are designated by bromoantimonate(III) or bromoantimonate(V). Although antimony tribromide is known, SbBr5 on its own does not exist, despite the existence of SbRb−6.[1] Compounds containing both Sb(III) and Sb(V) are mixed valence compounds. The antimony can be linked into chains, (which are called one-dimensional as it is like a line), or in pairs as Sb2 or singly as Sb (which are called zero-dimensional, as the anions are just point-like).
Tetrabromoantimonate(III) (SbBr4−) has single antimony atoms in each anion.[2]
SbBr52− contains infinite chains of SbBr6 octahedra linked by corners.[3]
Hexabromoantimonate(III) SbBr63− also exists, forming zero-dimensional compounds.[4]
Nonabromodiantimonate(III) Sb2Br93− has a pair of octahedra of SbBr6 sharing a face. The angles formed by shared bromine at the antimony are reduced from the theoretical 90° to about 80°.[5]
Hexabromoantimonate(V) SbBr6− exists in equilibrium with SbBr4− and Br2 but real +5 oxidation state bromoantimonates exist even if SbBr5 is unstable and does not exist.[6][7] [8]
Intersecting classes are nonahalogenodiantimon(III)ates. Hexahaloantimonate(III) ions (SbX63−) can include chlorine or iodine as well as bromine.[9]
Related classes include halogeno-oxydiantimon(III)ates, and pentabromothio‐diantimonates.[10] Bromo-phenylantimonates(V) (C6H5SbBr5) have a phenyl group substituting for one bromine atom.[11] Chlorobromoantimonates(V) have some chlorine instead of bromine.[12]
The antimonide bromides are distinct as they do not have a bond between antimony and bromine. Tetrabromostibonium(V) contains cations (SbBr+4) rather than anions.[13]
Preparation
Bromoantimonates can be made using a water solution of antimony tribromide, hydrobromic acid, and an amine. Alternately antimony trioxide can be used. Variants can be made without using water, and heating the antimony tribromide with an amine hydrobromide.[14]
Some properties
Most of the bromoantimonate salts are yellow or orange.[15]
For SbBr−4 there are absorption bands at 224, 300, 245 and 216 nm. SbBr3−6 has absorption bands centred on 359, 311, and 266 nm.[16]
Many alkylammonium salts are known. These can have different solid phases at different temperatures, as the alkyl group varies in disorder. Those with longer alkyl chains have a greater number of solid state phases.[17]
Methyl ammonium compounds are ferroelectric.[17]
The infrared spectrum includes wavenumbers (ν/c) of 110 to 130 cm−1 for the bridging bromine in Sb2Br9 and 135 to 220 cm−1 for non-bridging bromine to antimony stretching.[18]
Bond lengths in SbBr6− are 2.65 and 2.56 Å. In SbBr63− the lengths are greater, from 2.787 to 2.713 Å.[19]
Use
Bromoantimonates are researched for use in photovoltaics,[20] X-ray detectors,[21] and LEDs.[22]
List
Name (full or part) | Formula | System | Space group | Unit cell (Å) | Volume | Density | Notes | Ref |
---|---|---|---|---|---|---|---|---|
ammonium | [H4N]2SbBr6 | tetragonal | I41/amd | a=10.66 c=21.52 | black; Sb(III) and Sb(V) | [7][23] | ||
ammonium | (NH4)3Sb2Br9 | inefficient photovoltaic; soluble in ethanol | [24] | |||||
ammonium | (NH4)7Sb3Br16 | [25] | ||||||
guanidinium | [C(NH2)3]SbBr6 | black; Sb(V) | [26] | |||||
guanidinium | [C(NH2)3]3Sb2Br9 | monoclinic | C2/c | a = 15.695 b = 9.039 c = 18.364 β = 96.94° Z=4 | @143K; phase transition 435/450 K | [27][28] | ||
Tris(N,N,N',N'-tetramethylguanidinium) nonabromodiantimonate(III) | [NH2C(N(CH3)2)2]3[Sb2Br9] | triclinic | P1 | a 10.9824 b 12.1782 c 15.0405 α 71.064° β 88.199° γ 85.024° | [29] | |||
methylammonium | (CH3NH3)3SbBr6 | monoclinic | P21/c | a=13.577 b=8.254 c=21.665 β=134.05° Z=4 | [30] | |||
methylammonium bromoantimonate(III) | (CH3NH3)3Sb2Br9 | P3m1 | a=8.188 c=9.927 Z=1 | 3.049 | yellow | [31][32] | ||
dimethyl ammonium | [(CH3)2NH2]3SbBr6 | [30] | ||||||
tris (dimethylammonium) nonabromodiantimonate(III) | [(CH3)2NH2]3Sb2Br9 | monoclinic | P21/a | a = 14.612 b = 9.228 c = 10.005 β = 94.91° Z = 2 | [33] | |||
[NH2(CH3)2]3Sb2Br9 | ||||||||
tris(Trimethylammonium) nonabromodiantimonate(III) | [(CH3)3NH]3Sb2Br9 | orthorhomic | a 11.40 b 10.31 c 12.91 | [34] | ||||
tetramethylammonium | [NMe4]3[Sb2Br9] | hexagonal | P63/mmc | a=9.499 c=22.225 Z=2 | crimson red | [35][36] | ||
tetramethylammonium | [NMe4]3[Sb2Br9]•Br2 | hexagonal | P63/mmc | a=9.585 c=22.667 Z=2 | [37] | |||
tetramethylammonium | [(CH3)4N]3Sb3Br9•Br2 | hexagonal | P63/mmc | a=9.5850 c=22.667 Z=2 | 2.48 | red; yellow-orange when cold | [38] | |
tetramethylammonium | [(CH3)4N]3Sb2Br9•I2 | triclinic | P1 | a=9.4869 b=9.5409 c=22.4906 α=92.058° β=90.933° γ=118.386° Z=2 | 1788.5 | dark | [39] | |
ethylammonium | (C2H5NH3)2[SbBr5] | orthorhombic | Cmca | a= 7.815 b=22.301 c=18.100 Z=8 | 3154.5 | 2.584 | at 298K; yellow; phase transition at 158.5K; decompose >450K | [15][30] |
ethylammonium | (C2H5NH3)2[SbBr5] | orthorhombic | Pbca | a=7.684 b=22.413 c=17.780 Z=8 | 3062.1 | 2.661 | at 90K; yellow | [15] |
ethylammonium | (C2H5NH3)2[SbBr7] | [40] | ||||||
diethylammonium | ([C2H5]2NH2)3SbBr6 | hexagonal | R3c | a=15.155 c=20.085 Z=6 | dissolves in acetone | [41][34] | ||
tetraethylammonium | [(C2H5)4N]2SbBr6 | very dark reddish brown | [7] | |||||
tetraethylammonium | [(C2H5)4N]3Sb2Br9 | hexagonal | P6322 | a=10.3 c=24.4 Z=2 | 2242 | 2.02 | yellow | [42][43] |
tetraethylammonium hexabromoantimonate(V) | [(C2H5)4N]SbBr6 | tetragonal | I41md | a=8.7008 c=24.797 Z=4 | 1877.3 | 2.59 | dark red-brown | [44][45] |
n-propylammonium | (n-C3H7NH3)2SbBr5 | orthorhombic | ? | a =7.884 b=14.516 c=15.913 Z=4 | 1821.1 | 2.33 | 4 phase transitions: 189K, 165/163, 137/154 | [46][30][47] |
di-n-propylammonium | [(n-C3H7)2NH2]3SbBr6 | hexagonal | R3c | a=13.649 c=31.548 Z=6 | dissolves in acetone | [41] | ||
tris(Tri-n-propylammonium) nonabromodiantimonate(III) | [(n-C3H7)3NH]3Sb2Br9 | orthorhombic | ? | a 12.91 b 14.51 c 20.0 | [34] | |||
bis(Isopropylammonium) pentabromoantimonate(III) | [(i-C3H7)2NH2]2SbBr5 | orthorhombic | a 14.99 b 16.687 c 21.72 | [34] | ||||
tetrapropylammonium | [(C3H7)4N][SbBr4] | orthorhombic | Pbca | a=15.566 b=13.822 c=19.574 Z=8 | 4211.5 | yellow | [48] | |
isopropylammonium | [(CH3)2CHNH3]2SbBr5 | orthorhombic | a=12.013 b =12.134 c=12.525 | phase transition at 171K, 180 K | [49] | |||
isopropylammonium | [(CH3)2CHNH3]2SbBr5 | monoclinic | [50] | |||||
tris(N-ethyl-N,N-dipropylpropan-1-aminium) tetrakis(μ-bromo)-octabromo-tri-antimony | (Et(n-Pr)3N)3[Sb3Br12] | triclinic | P1 | a 10.6469 b 14.8847 c 18.3714 α 86.082° β 85.502° γ 84.116° | [51] | |||
isobutyl | (i-C4H9NH3)2SbBr5 | [52] | ||||||
ethanediammonium | [NH3(CH2)2NH3]5(Sb2Br11)2·4H2O | monoclinic | P21/a | a = 14.346 b = 13.206 c = 17.027 β = 113.05° Z = 2 | 2.941 | [53] | ||
N,N,N',N'-tetramethylethylendiammonium [tetrabromidoantimonate(III)-μ-bromido] hemihydrate | (C6H18N2)2[Sb2Br10]·H2O | orthorhombic | Pbca | a = 18.0860 b = 19.1755 c = 19.4619 Z=8 | 6749.5 | 2.553 | yellow | [54] |
anilinium | (C6H5NH3)2SbBr5 | orthorhombic | Pbca | a = 19.704 b = 7.914 c = 25.556, Z = 8 | 3985 | 2.365 | yellow green; insoluble water | [3] |
dihydrazinium pentabromoantimonite | (N2H5)2SbBr5 | yellow | [25] | |||||
Trihydrazinium nonabromodiantimonite | (N2H5)3Sb2Br9 | yellow | [25] | |||||
Undecahydrazinium heptadecabromodiantimonite | (N2H5)11Sb2Br17 | yellow; melt 165° | [25] | |||||
Decahydrazinium nonadecabromotriantimonite | (N2H5)10Sb3Br19 | yellow | [25] | |||||
triazolinium | (C2H4N3)2[SbBr5]·(C2H4N3)Br | orthorhombic | P212121 | a=8.6087 b=11.7985 c=20.5457 | [55] | |||
1,2,4-triazolium | (C2N3H4)3[SbBr6] | tetragonal | P42/m | a=11.149 c=8.318 Z=2 | 1033.9 | 2.606 | @320K | [56] |
1,2,4-triazolium | (C2N3H4)3[SbBr6] | monoclinic | a=15.699 b=16.294 c=15.018 β = 90.41 Z=8 | 4097 | 2.631 | @293K | ||
allylammonium | (C3H5NH3)3SbBr6 | monoclinic | C2/m | 4 phases | [57] | |||
butylammonium | [n-C4H9NH3]2•[SbBr5] | orthorhombic | Pnma | a=16.845 b=54.899 c=15.697 | 340K deep yellow; 3 phases | [58] | ||
butylammonium | [n-C4H9NH3]2•[SbBr5] | monoclinic | P2/m | a=15.597, b=62.854, c=16.771 β=92.05° | 300K | [58] | ||
tris(n-Butylammonium) hexabromo-antimony(III) | [n-C4H9NH3]3•[SbBr6] | a 11.47 b 15.07 c 18.57 | [34] | |||||
di-n-butylammonium | [(n-C4H9)2NH2]3•[SbBr6] | monoclinic | P21/c | a 13.03 b 13.51 c 18.94 β 94.0° | [30][34] | |||
tetra-n-butylammonium hexa-bromoantimonate(V) | [(n-C4H9)4N]•[SbBr6] | [44] | ||||||
pentylammonium | [n-C5H11NH3]2•[SbBr5] | orthorhombic | Pna21 | a=17.0105 b=32.875 c=7.8882 | 298K; 3 phases transitions at 388K 224K | [17] | ||
pentylammonium | [n-C5H11NH3]2•[SbBr5] | orthorhombic | P212121 | a=16.9234 b=32.3689 c=7.7418 | 86K | [17] | ||
2,2-difluoroethylammonium | [C2H6F2N]3SbBr6 | monoclinic | P121/n1 | a=8.0145 b=12.1192 c=21.2967 β=91.686 Z=4 | 2067.6 | 2.722 | yellow | [59] |
N-ethyl-1,3-propanediammonium | [C5N2H16]2SbBr5 | monoclinic | P21/c | a=21.426 b=7.889 c=19.96 β=116.79° Z=8 | 3012 | [60] | ||
N-ethyl-1,3-propanediammonium | [C5N2H16]2SbBr5 | orthorhombic | Pnma | a=19.23 b=7.894 c=10.118 Z=4 | 1536 | yellow | [60] | |
bis(N,N-diethylethylendiammonium) decabromodiantimoinate(III) | [C6H18N2]2Sb2Br10 | monoclinic | P21/c | a = 10.7309 b = 10.5842 c = 14.5551 β = 96.962° Z = 4. | yellow | [61] | ||
1,5-pentanediammonium pentabromoantimonate (III) | [NH3(CH2)5NH3]SbBr5 | orthorhombic | P212121 | a 7.964 b 13.9424 c 14.065 | @293K | [62] | ||
1,5-pentanediammonium pentabromoantimonate (III) | [NH3(CH2)5NH3]SbBr5 | orthorhombic | Pnma | a 14.04 b 8.04 c 13.97 | @393K | [62] | ||
Ethyldimethylphenylammonium | [EtMe2PhN]3[Sb2Br9] | orthorhombic | Pnma | a = 35.620 b = 9.954 c = 12.761 Z = 4 | [63] | |||
Tris(N,N-dimethylanilinium) tri--bromido-bis[tribromidoantimonate(III)] | (C8H12N)3[Sb2Br9] | triclinic | P1 | a 9.7857(b 13.7658(c 17.0297(α 66.581( β 78.689( γ 72.601( Z=2 | [64] | |||
[CH3SC(NH2)2]2SbBr5 | 11.4258 b=8.9079 c=17.3627 β=92.225 Z=4 | 1765.8 | 2.647 | [65] | ||||
cyclopropylammonium | [C3H8N]2SbBr5 | monoclinic | P21/c | a=11.8937 b=19.0986 c=7.8047 β = 108.908° | 1168.0 | 2.525 | 270K | [66] |
cyclopropylammonium | [C3H8N]2SbBr5 | orthorhombic | Pnca | a=22.5314 b=18.9885 c=7.8845 Z=8 | 2336.0 | 2.511 | 300K | [66] |
cyclopropylammonium | [C3H8N]2SbBr5 | orthorhombic | Bbcm | a=22.4485 b=18.9653 c=7.9488 Z=8 | 2256 | 2.503 | 325K; band gap 2.41 eV; phase changes at 290 K and = 315 K | [66] |
Benzeneethanammonium | (C8NH12)2SbBr5 | yellow | [67] | |||||
phenylmethylammonium | (C6H5CH2NH3)3SbBr6 | monoclinic | P21/c | a 15.2246 b 8.0632 c 24.3042 β 100.005° Z=4 | 2938.2 | 2.093 | yellow | [68] |
(R)-(−)-1-cyclohexylethylammonium | (R-CHEAH)Sb3Br10 | monoclinic | P21 | a=12.76938 b=30.1777 c=13.2336 β=90.818 | [69] | |||
Pyrrolidinium | [C4H9N]2SbBr8 | monoclinic | a=31.4 b=9.71 c=15.0 β=99.0° Z=8 | 4517 | 2.50 | black | [70] | |
2-Pyrolidonium | [C4H6ONH]2SbBr8 | black; orange red when cold | [70] | |||||
N-methylpyrrolidinium | [C4H9NCH3]3Sb2Br9 | trigonal | R3c | a=15.6943 c=15.6943 Z=6 | 5018.8 | 2.424 | yellow @293K | [71] |
N-methylpyrrolidinium | [C4H9NCH3]3Sb2Br9 | trigonal | R3c | a=15.9951 c=23.1124 Z=5 | 5120.9 | 2.376 | @335K | [71] |
Piperidinium | [C5H11N]2SbBr8 | monoclinic | a=28.8 b=19.8 c=18.7 β=116.28 Z=16 | 9561 | 2.58 | black | [70] | |
Piperazine-1,4-diium | (C4H12N2)[SbBr5]·H2O | monoclinic | P21/n | a=9.9162 b=14.4090 c=10.3898 β=99.432 Z=4 | 1464.45 | 2.846 | [72] | |
Morpholinium | [NH2(C2H4)2O]SbBr4 | orthorhombic | Pbca | a=12.273 b=8.397 c=23.276 Z=8 | 2399 | 2.933 | yellow | [73] |
Morpholinium | [NH2(C2H4)2O]2[SbBr5] | orthorhombic | P212121 | a 9.274 b 10.325 c 18.472 Z=4 | 1768.8 | 2.620 | yellow; piezoelectric | [74] |
Morpholinium | [C4H9ONH]2SbBr8 | orthorhombic | Pna21 | a=28.01 b=8.31 c=10.02 Z=4 | 2332 | 2.64 | black; red when cold | [70] |
Pyridinium | (C5H5NH)SbBr4 | triclinic | P1 | @116K | [75] | |||
Pyridinium | (C5H5NH)SbBr4 | monoclinic | C2/c | a=11.825 b=13.048 c=7.798 β=93.87° Z=4 | 2.922 | @297K | [57][75] | |
Pyridinium | (C5H5NH)6SbIIISbV3Br24 | orthorhombic | CmC21 | a=17.51 b=23.77 c=16.46 Z=4 | 6851 | 2.80 | black | [70] |
benzylammonium | (C6H5CH2NH3)2SbBr5 | monoclinic | P21/a | a=8.0254 b=19.5087 c=14.5079 β=107.451 Z=4 | 2166.89 | 2.261 | yellow | [76] |
1-methylpyridinium | (1−CH3C5H4NH)SbBr4 | monoclinic | P21/c | a=12.73 b=13.54 c=7.59 β=107.3 Z=4 | 1250 | 2.85 | pale yellow | [77] |
bis(1-methylpyridin-1-ium) hexabromo-antimony tribromide | (1−CH3C5H4NH)2SbBr6•Br3 | triclinic | P1 | a 7.4567 b 9.4488 c 9.6777 α 68.629° β 89.848° γ 73.002° | 1029.2 | [78] (1) | ||
2-methylpyridinium | (2−CH3C5H4NH)SbBr4 | monoclinic | P21/c | a=12.84 b=13.31 c=7.65 β=106.6 Z=4 | 1252 | 2.84 | pale yellow | [77] |
3-methylpyridinium | (3−CH3C5H4NH)SbBr4 | monoclinic | P21/c | a=12.51 b=13.64 c=7.72 β=106.9 Z=4 | 1260 | 2.76 | pale yellow | [77] |
bis(2-bromo-5-methylpyridinium) hexabromoantimonate tribromide | (2-Br-5-MePy)2[SbBr6](Br3) | monoclinic | Im | a 8.4041 b 13.341 c 12.237 β 95.731° | [79] | |||
3-carboxylpyridinium | (3−COOHC5H4NH)2SbBr5 | monoclinic | C2/c | a=14.10 b=19.43 c=8.01 β=98.6° Z=4 | 2169 | 2.36 | lemon yellow | [77] |
4-methylpyridinium | (4−CH3C5H4NH)SbBr4 | monoclinic | P21/c | a 12.011 b 13.581 c 7.7637 β 90.341° | [80] | |||
4-methylpyridinium | (4−CH3C5H4NH)2SbBr5 | triclinic | P1 | a=10.66 b=10.86 c=9.30 α=108.8° β=97.7° γ=99.2° Z=2 | 985 | 2.39 | yellow needles | [57][77][81] |
4-methylpyridinium | (4−CH3C5H4NH)3Sb2Br9•I2 | monoclinic | P21 | a=8.3290 b=23.5510 c=9.4722 β=104.388 Z=2 | 1799.7 | [39] | ||
4-methylpyridinium | (4−CH3C5H4NH)2SbBr5•I2 | monoclinic | P21/n | a=7.5955 b=14.6757 c=9.5902 β=91.607 Z=2 | 2182.85 | [39] | ||
4-methylpyridinium | (4-C6H7NH)2SbVBr9 | monoclinic | C2/m | a=18.39 b=7.440 c=9.84 β=113.14° | 2.760 | red | [82] | |
α-picolinium | (2−CH3C5H4NH)2SbBr9 | triclinic | P1 | a 9.249 b 9.750 c 7.645 α 90.07° β 107.46° γ 70.52° Z=2 | 2.77 | black; orange at −174° | [70][83] | |
β-picolinium | (3−CH3C5H4NH)2SbBr9 | monoclinic | Z=2 | 2.74 | black; orange at −174° | [70] | ||
γ-picolinium | (4−CH3C5H4NH)2SbBr9 | monoclinic | Z=2 | 2.77 | black; red at −174° | [70] | ||
1-fluoropyridinium | (1-FPy)3[Sb2Br9] | monoclinic | C2/c | a=21.85 b=21.15 c=13.85 β=104.6° Z=8 | 6179 | 2.70 | deep yellow | [77] |
1-bromopyridinium | ? | monoclinic | C2/c | a=11.83 b=13.03 c=7.70 β=93.9° | 1183 | 2.4 | light orange | [77] |
2-chloropyridinium | (2-ClPyH)2SbBr5 | monoclinic | P21/a | a=10.64 b=15.87 c=5.88 β=105.3° Z=2 | 957 | 2.60 | orange | [77] |
2-chloropyridinium | (2-ClPyH)SbBr6 | monoclinic | P21/c | a=13.0770 b=7.3498 c=16.5301 β=112.117° | Sb(V) | [84] | ||
2-bromopyridinium | (2-BrPyH)2SbBr5 | monoclinic | P21/a | a=10.53 b=16.17 c=5.89 β=104.8° Z=2 | 989 | 2.82 | red | [77] |
2-bromopyridinium | (2-BrPyH)SbBr6 | monoclinic | P21/c | a=13.111 b=7.3787 c=16.555 β=111.179° | Sb(V) | [84] | ||
bis(2-iodopyridinium) hexabromoantimonate tribromide | (2-IPyH)2[SbBr6](Br3) | monoclinic | P21/n | a 8.1800 b 12.9394 c 12.5865 β 105.412° | [79] | |||
3-chloropyridinium | (3-ClPyH)SbBr6 | orthorhombic | Pca21 | a=16.6414 b=7.3471 c=24.2543 Z=8 | 2965.5 | cherry-red | [85] | |
3-bromopyridinium | (3-BrPyH)2SbBr5 | monoclinic | P21/c | a=18.37 b=11.98 c=9.35 β=102.5° Z=4 | 2009 | 2.77 | pale yellow | [77] |
3-bromopyridinium | (3-BrPyH)SbBr6 | orthorhombic | Pca21 | cherry-red | [85] | |||
3-iodopyridinium | (3-IPyH)2SbBr5 | monoclinic | P21/c | a=17.99 b=12.31 c=9.35 β=91.5° Z=4 | 2070 | 2.99 | pale yellow | [77] |
4-bromopyridinium pentabromoantimonate(III) | (4-BrC5H4NH)2SbBr5 | triclinic | P1 | a = 9.186 b = 10.622 c = 10.703 α = 99.665° β = 97.393° γ = 108.539° Z = 2 | [86] | |||
bis(4-bromopyridinium) hexabromoantimonate tribromide | (4-BrPyH)2[SbBr6](Br3) | monoclinic | P21/c | a 7.3255 b 20.667 c 16.5665 β 95.627° | [79] | |||
2,6-dichloropyridinium | (2,6-ClPyH)[SbBr4] | monoclinic | P2/m | a=10.45 b=10.76 c=13.45 β=110.2 Z=4 | 1491 | 2.76 | pale yellow | [77] |
2,6-dibromopyridinium | (2,6-BrPyH)3[SbBr6](Br3) · 2H2O | monoclinic | C2/c | a=32.8242 b=9.6155 c=14.7877 β=101.732° | [87] | |||
3,5-dichloropyridinium | (3,5-ClPyH)2[SbBr5] | orthorhombic | Pbca | a=21,77 b=8.14 c=24.38 Z=8 | 4320 | 2.52 | deep yellow | [77] |
N-ethylpyridinium | EtPySbBr6 | [88] | ||||||
N-propylpyridinium | 1-n-PrPySbBr6 | monoclinic | P21/n | a=7.3687 b=16.4706 c=13.8620 β=97.054 Z=4 | 1669.65 | [79] (1) | ||
N-butylpyridinium | 1-n=BuPySbBr6 | orthorhombic | P212121 | a=7.4277 b=14.1293 c=16.7699 Z=4 | 1760.0 | [79] (2) | ||
2-aminopyridinium | [2-NH2C5H4NH][SbBr4] | monoclinic | P21/c | a 12.484 b 13.106 c 7.492 β 105.84° Z=4 | 1179.1 | 3.022 | @100K phase transition at 396/412K | [89] |
4-aminopyridinium | (4-NH2C5H4NH)SbBr4 | monoclinic | P21/c | a 11.548 b 14.029 c 7.432 β 93.19° | @220K | [90] | ||
tetrakis(2,2'-bipyridin-1-ium) tetrakis(μ-bromo)-hexadecabromo-tetra-antimony | (2,2′-bipyH)4[Sb4Br20] | monoclinic | P21/c | a 14.5026 b 14.6945 c 16.5497 β 109.991° | [51] | |||
bis(pyridinium)ethane | (PyC2){[SbBr6](Br3)} | triclinic | P1 | a=7.3269 b=9.1941 c=9.7994 α=64.474 β=80.207 γ=86.244 Z=1 | 586.99 | cherry-red | [91] | |
1,1′-(1,2-ethanediyl)bis(pyridine) | PyC22+SbBr5 | triclinic | P1 | a 10.1060 b 10.2956 c 11.1394 α 105.030° β 101.709° γ 117.233° | [92] | |||
1,1′-(1,2-ethanediyl)bis(3,5-dimethylpyridine) | 3,5-MePyC22+SbBr5 | monoclinic | P2/n | a 6.2898 b 8.7454 c 20.408 β 90.438° | [92] | |||
1,1′-(1,2-ethanediyl)bis(pyridine) | (C2Py)2[Sb2Br10] | triclinic | P1 | a 6.1343 b 9.2857 c 17.2041 α 90.331° β 100.259° γ 99.912° | [92] | |||
1,1′-(1,2-ethanediyl)bis(pyridine) | (C2Py)2[Sb2Br10] | monoclinic | C2/c | a 19.6880 b 10.0152 c 20.8410 β 111.104° | [92] | |||
1,1′-(1,2-ethanediyl)bis(3,5-dimethylpyridine) | (3,5-MePy){[SbBr4]} | monoclinic | P21/n | a 20.5536 b 7.2974 c 21.2510 β 117.694° | [92] | |||
bis(pyridinium)propane | (PyC3)2[Sb2Br9][SbBr6] | orthorhombic | Pmmm | a=20.3785 b=15.5018 c=7.4618 Z=2 | 2357.2 | mixed III V valence | [91] | |
bis(pyridinium)butane | (PyC4){[SbBr6](Br3)} | triclinic | P1 | a=7.8627 b=9.1285 c=10.1514 α=68.392° β=89.669° γ=72.048° Z=1 | 639.63 | [91] | ||
4-ethylpyridinium | (4−CH3CH2C5H4NH)3Sb2Br14 | orthorhombic | Pna21 | Z=4 | 2.55 | black; orange-red at −174° | [70] | |
1,1′-(propane-1,3-diyl)bis(4-methylpyridin)-1-ium | (4-MePyC3)2[SbBr6]2[Br5]2 | monoclinic | P21/n | a=7.7157 b=16.1786 c=24.292 β=96.972° | Sb(V) | [93] | ||
propanediyl-bis(3-methylpyridinium) | (3-MePyC3)3[Sb4Br16] | monoclinic | P21/n | a 11.6777 b 42.282 c 16.5504 β 95.618° | [94] | |||
1,1'-(ethane-1,2-diyl)bis(3-methylpyridin-1-ium) | (3-MePyC2)3[Sb2Br9]2 | triclinic | P1 | a 10.6368 b 10.8059 c 15.4810 α 76.034° β 81.735° γ 83.387° | [94] | |||
bis(1,1'-(butane-1,4-diyl)bis(3-methylpyridin-1-ium)) hexakis(μ-bromo)-decabromo-tetra-antimony(iii) | (3-MePyC4)3[Sb4Br16] | monoclinic | P21/n | a 14.2410 b 11.2731 c 19.0662 β 110.674° | [94] | |||
4,4'-dimethyl-1,1'-butanediylbis(pyridinium) | (4-MePyC4)[Sb2Br8] | monoclinic | P 2/c | a 26.313 b 6.4010 c 17.9886 β 109.026° | [95] | |||
4,4'-dimethyl-1,1'-butanediylbis(pyridinium) | (4-MePyC4)2[Sb4Br16] | monoclinic | P21/n | a 11.4661 b 19.7236 c 12.5217 β 92.726° | [95] | |||
1,3,4-trimethylpyridin-1-ium | 1,3,4-MePy[SbBr6] | triclinic | P1 | a 8.3195 b 8.9921 c 12.3360 α 86.146° β 76.520° γ 71.872° | Sb(V) | [96] | ||
1,4-dimethylpyridin-1-ium | 1,4-MePy[SbBr6] | triclinic | P1 | a 7.6803 b 8.5900 c 12.6261 α 75.226° β 88.079° γ 79.872° | Sb(V) | [96] | ||
1,2-dimethylpyridinium | (1,2-MePy)2[SbBr6](Br3) | monoclinic | P21/n | a=7.3284 b=10.5875 c=16.7538 β=96.005° | Sb(V) | [96] | ||
1,3-dimethylpyridinium | (1,3-MePy)2[SbBr6](Br3) | triclinic | P1 | a 7.2611 b 9.086 c 11.1895 α 67.617° β 87.457° γ 72.16° | [79] (5) | |||
2,4-dimethylpyridinium | ? | orthorhombic | Pmmn | a=12.06 b=12.97 c=11.49 | 1797 | 2.2 | yellow | [77] |
2,6-dimethylpyridinium | (2,6-MePy)3[Sb2Br9] | monoclinic | P21/c | a=12.10 b=15.56 c=21.27 β=115.7 Z=4° | 3629 | 2.36 | pale yellow | [77] |
1-ethyl-3-methylpyridinium | (1-Et-3-MePy)2[SbBr6](Br3) | triclinic | P1 | a 7.2472 b 9.4088 c 11.5541 α 69.263° β 81.162° γ 71.303° | [79] | |||
4-ethyl-1-methylpyridinium | (4-Et-1-MePy)2[SbBr6](Br3) | monoclinic | P21/n | a 8.4645 b 13.0802 c 13.1574 β 105.702° | [79] | |||
bis(2,6-dimethylpyridin-1-ium) hexabromo-antimony pentabromide | (2,6-MePy)2[SbBr6](Br5) | monoclinic | P21/c | a 7.4584 b 18.0860 c 21.626 β 93.607° Z=4 | 2911.4 | [78] (3) | ||
bis(1,3,5-trimethylpyridin-1-ium) hexabromo-antimony tribromide | (1,3,5-MePy)2[SbBr6](Br3) | triclinic | P1 | a 8.1964 b 8.2015 c 12.5202 α 92.883° β 103.923° γ 115.467° Z=4 | 1085.3 | 100K | [78] (4) | |
2,4,6-trimethylpyridinium | (2,4,6-MePy)3[Sb2Br9] | monoclinic | P21/n | a=10.36 b=42.36 c=9.09 β=100.2° Z=4 | 3926 | 2.25 | yellow-tan | [77] |
2,4,6-trimethylpyridinium | (2,4,6-MePy)[SbBr]•0.5Br2 | monoclinic | P21/n | a 10.4938 b 13.6198 c 12.8807 β 90.339° Z=4 | 1840.9 | 100k | [78] (5) | |
bis(3,5-dimethylpyridin-1-ium) hexabromo-antimony tribromide | (3,5--MePy)2[SbBr6](Br3) | orthorhombic | Pnnm | a 17.1097 b 10.4401 c 7.3438 Z=2 | 1311.8 | [78] (2) | ||
bis(1-ethyl-3-methylpyridinium) hexabromoantimonate tribromide | (1-Et-3-MePy)2[SbBr6](Br3) | triclinic | P1 | a 7.2472 b 9.4088 c 11.5541 α 69.263° β 81.162° γ 71.303° | [79] | |||
1-ethyl-4-methylpyridin-1-ium | (1-Et-4-MePy)2[SbBr6](Br3) | monoclinic | P21/n | a=11.4927 b=7.3613 c=16.9266 β=100.782° | Sb(V) | [96] | ||
1-ethyl-2-methylpyridin-1-ium | (1-Et-2-MePy)2[SbBr6](Br3) | monoclinic | P21/n | a=8.3421 b=13.196 c=13.183 β=105.40° | Sb(V) | [96] | ||
1-ethyl-2,6-dimethylpyridin-1-ium hexabromoantimonate | (1-Et-2,6-MePy)[SbBr6] | monoclinic | P21/c | a 9.9470 b 11.5017 c 16.4632 β 107.201° | [79] | |||
(PyC3)3[Sb2Br9]2 | [97] | |||||||
(PyC4)[Sb2Br8] | [97] | |||||||
(PyC5)2[α-Sb4Br16] | [97] | |||||||
(PyC6)2[Sb2Br10] | [97] | |||||||
(4-MePyC2)2[Sb2Br10] | [97] | |||||||
(4‑MePyC3)2[α-Sb4Br16] | [97] | |||||||
(4-MePyC5)2[α-Sb4Br16] | [97] | |||||||
1-benzylpyridin-1-ium hexabromoantimonate | C6H5CH2PySbBr6 | orthorhombic | Pnma | a=12.6594 b=17.3414 c=8.6389 Z=4 | 1896.5 | [78] (6) | ||
bis(1-benzyl-2-methylpyridinium) hexabromoantimonate tribromide | (CH3-C6H5CH2Py)2SbBr6(Br3) | triclinic | P1 | a 8.9834 b 10.2599 c 10.3601 α 94.223° β 102.737° γ 111.846° | [79] (7) | |||
bis(1-(4-bromobenzyl)pyridinium) hexabromoantimonate tribromide | (BrC6H4CH2Py)2SbBr6(Br3) | monoclinic | P21/c | a 8.6483 b 15.1885 c 13.3520 β 98.887° | [79] | |||
2,2'-bipyridinium pentabromoantimonate (III) | (2,2'-C10H8N2H2)SbBr5 | monoclinic | P21/c | a = 14.575 b = 14.726 c = 16.775 β = 110.34° Z = 8 | [98] | |||
4,4'-bipyridinium pentabromoantimonate (III) | (4,4'-C10H8N2H2)SbBr5 | triclinic | P1 | a = 11.28.7 b = 10.121 c = 8.548 α = 98.94° β = 101.06° γ = 113.57° Z = 2 | [98] | |||
imidazolium | (C3N2H5)3SbBr6.H2O | monoclinic | P21/c | a=8.9137 b=19.2032 c=12.7984 β=90.650° | [99] | |||
imidazolium | (C3N2H5)5Sb2Br11 | monoclinic | P21/n | a 9.1399 b 15.150 c 13.969 β 96.19° | ferroelectric Curie Point 145K; 4 phases | [99][100] | ||
thiazolium | (C3H4NS)6Sb4Br18·2H2O | triclinic | P1 | a 11.060 b 11.465 c 12.957 α 116.21° β 100.71° γ 98.87° | [101] | |||
quinolinium | monoclinic | Cc | a=15.28 b=14.04 c=7.44 β =118.3 Z=4 | 1405 | 2.70 | light yellow | [77] | |
quinolinium | (C9H7NH)2SbBr9 | monoclinic | P21/n | as=7.518 b=11.316 c=16.351 β =97.41 Z=2 | Sb(V) | [102] | ||
3-Bromoquinolinium | (3-BrQuinH)4[Sb2Br10] | monoclinic | C2/c | a 15.3947 b 13.7967 c 22.8880 β 92.039° | [103]2 | |||
5-Bromoquinolinium | (5-BrQuinH)2[SbBr5] | monoclinic | C2/c | a 23.8681 b 12.2567 c 8.6474 β 106.128° | [103]3 | |||
3-Bromo-1-methylquinolinium | (1-Me-3-BrQuin)3[Sb3Br12] | triclinic | P1 | a 9.8582 b 11.7183 c 21.6576, α 98.981° β 96.402° γ 92.371° | [103]5 | |||
isoquinolinium | isoquinHSbBr4 | monoclinic | P21/a | a=13.11 b=14.14 c=7.57 β=91.4 Z=4 | 1403 | 2.71 | light tan | [77] |
N-methyl quinolinium | (N-MeQuin)2{[SbBr6](Br3)} | triclinic | P1 | a=8.0902 b=8.5656 c=11.6475 𝛼 = 68.901° β = 79.204° 𝛾 = 77.120° Z=1 | 728.98 | [104] | ||
N-methyl isoquinolinium | (N-MeIsoquin)2{[SbBr6](Br3)} | monoclinic | P21/c | a=12.9656 b=9.3423 c=12.5920 β = 107.233° Z=2 | 1456.8 | [104] | ||
N-ethyl quinolinium | (N-EtQuin)[SbBr6] | orthorhombic | Pnma | a=14.5122 b=11.4005 c=11.2135° Z=4 | 1855.2 | [104] | ||
tris(6-methylquinolinium) hexabromoantimonate(III) | (6-MeQuin)3[SbBr6] | [105] | ||||||
2-methyl-1,3-benzoxazole | SbBr5(boxH)2 | triclinic | P1 | a=8.560 b=11.008 c=12.751 α=102.836° β=106.173° γ=93.398° | [106] | |||
quinuclidinium | (C9H7NH)2SbVBr9 | monoclinic | P21/n | a=7.518 b=11.316 c=16.351 β=97.41° Z=2 | 2.67 | red | [107] | |
quinuclidinium | (C7H13NH)4SbIIISbVBr12.2Br2 | cubic | Fm3m | a=13.873 | 2670 | 2.45 | black | [108] |
3-ammoniumpropyl imidazolium pentabromoantimonate (III) | [C6H13N3]2+[SbBr5]2− | orthorhombic | P212121 | 8.7120 b = 12.6608 c = 14.3498 Z = 4 | [109] | |||
trihydroxonium enneabromidodiantimonate(III) | (H3O)3Sb2Br9 | monoclinic | P21/n | a = 13.4679 b = 7.6319 c = 19.1397 β = 90.240° Z=4 | 1967.3 | 3.443 | yellow | [110] |
hexabromoantimonic(V) acid trihydrate | HSbBr6 · 3H2O | monoclinic | P21/c | a = 7.110 b = 13.532 c = 12.846 β = 94.87 Z=4 | melt 330K | [111] | ||
tetramethylphosphonium | [(CH3)4P]3[Sb2Br9] | hexagonal | P31/c | a 9.7931 c 22.697 | deep yellow | [112] | ||
trimethylphosphonium | [(CH3)3PH][SbBr4] | monoclinic | P21/c | a=10.9103 b=19.8342 c=11.3617 β=100.744 Z=4 | 2415.54 | 2.851 | colourless | [113] |
Methyltriphenylphosphonium | (MTP)6SbBr6Sb2Br9⋅H2O | trigonal | R3 | a=19.7793 c=27.2770 Z=3 | 9241 | 1.749 | [114] | |
Methyltriphenylphosphonium | (MTP)2SbBr5 | monoclinic | P21/c | a=12.7399 b=12.3833 c=26.0206 β=96.373 Z=4 | 4079.7 | 1.752 | [114] | |
tetraphenylphosphonium | P(C6H5)4SbBr6 | monoclinic | C2/c | a = 16.887 b = 7.357 c = 23.367 β = 93.98° Z=4 | 2896.1 | yellow | [115] | |
triphenyl(9-phenyl-9H-carbazol-3-yl) phosphonium antimony bromide | TPPcarzSbBr4 | triclinic | P1 | a=9.77183 b=11.42472 16.15939 α=88.2199° β=80.7810° γ=71.8474°, Z = 2 | 1691.77 | 1.857 | red LED | [22] |
Tetraphenylphosphonium Ikosioctabromooctaantimonate(III) | (PPh4)4Sb8Br28 | triclinic | P1 | a=12.491 b=13.078 c=21.523 α=102.93° β=100.83° γ= 100.42°, Z = 2 | 3273 | 2.318 | [116] | |
Tris-Chlorobromophosphazeno-carbenium | [C(NP(Br0,78Cl0,22)3)3]SbBr6 | orthorhombic | Pbca | a = 27.92 b = 11.23 c = 17.54 Z = 8 | [117] | |||
Rb3Sb2Br9 | monoclinic | P21/n | [118][119] | |||||
Rb4Sb2Br12 | tetragonal | I41/amd | a = 10.70 and c = 21.69 Z=8 | 4.17 | black | [26][120][19] | ||
Rb7Sb3Br16 | orthorhombic | Cmcm | a = 23.4716 b = 13.57.89 c = 35.3947 | yellow | [119][121] | |||
[RuNOPy4Br]4[Sb2Br8][Sb3Br12]2 | monoclinic | P21/c | a=12.021 b=22.454 c=26.372 β=92.506° Z=8 | 7112 | 2.634 | light orange | [122] | |
1,4-bis(ammoniomethyl)cyclohexane | (C8H20N2)2AgMBr8 | triclinic | P1 | a 8.0820 b 8.161 c 11.814 α 90.185° β 95.390° γ 90.121° | band gap 2.600 eV | [123] | ||
histammonium | (HIS)2AgSbBr8 | monoclinic | C2/c | a=11.5632 b=12.2529 c=18.694 β=94.264 Z=4 | 2641.3 | 2.754 | semiconductor; pale yellow | [21] |
Cs3Sb2Br9 | a=7.9165 c=9.7139 | yellow; orange at 300°C; perovskite | [124] | |||||
Cs4Sb2Br12 | tetragonal | I41/amd | a=10.842 c=21.913 Z=2 | 2576 | black @300K | [26][125] | ||
Cs2AgSbBr6 | cubic | Fm3m | a = 11.1583 Z=4 | 1389.2 | 4.661 | black; bandgap 1.64 eV | [117] | |
Benzeneethanammonium | (C8NH12)4Bi0.57Sb0.43Br7⋅H2O | triclinic | P1 | a=13.0207 b=13.1304 c=13.3192 α=93.818° β=102.408° γ=108.610° Z=2 | 2085.1 | 1.971 | light green | [67] |
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- ↑ Hubbard, Camden Richards (1971-09-01). "Crystal structure determinations of rubidium hexabromoantimonate (III, V) and tetramethylammonium nonabromodiantimonate (III) dibromine and a highly efficient white radiation neutron diffraction technique": IS–T–-476, 4709000. doi:10.2172/4709000.
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(help) - 1 2 3 Adonin, Sergey A.; Udalova, Liubov I.; Abramov, Pavel A.; Novikov, Alexander S.; Yushina, Irina V.; Korolkov, Ilya V.; Semitut, Evgeniy Y.; Derzhavskaya, Tatiyana A.; Stevenson, Keith J.; Troshin, Pavel A.; Sokolov, Maxim N.; Fedin, Vladimir P. (2018-10-01). "A Novel Family of Polyiodo-Bromoantimonate(III) Complexes: Cation-Driven Self-Assembly of Photoconductive Metal-Polyhalide Frameworks". Chemistry - A European Journal. 24 (55): 14707–14711. doi:10.1002/chem.201802100. PMID 30020549. S2CID 51676863.
- ↑ Rosenheim, Arthur; Stellmann, Wilhelm (October 1901). "Ueber die Pentahalogenide des Antimons und ihre Doppelverbindungen" (PDF). Berichte der Deutschen Chemischen Gesellschaft. 34 (3): 3377–3384. doi:10.1002/cber.19010340322. ISSN 0365-9496.
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- ↑ Miniewicz, A.; Jakubas, R.; Zaleski, J. (June 1991). "Measurements of pyroelectric properties in [(C 2 H 5 ) 4 N] 3 Sb 2 Br 9". Ferroelectrics. 118 (1): 23–28. Bibcode:1991Fer...118...23M. doi:10.1080/00150199108014740. ISSN 0015-0193.
- ↑ Zaleski, J.; Jakubas, R.; Galewski, Z.; Sobczyk, L. (1989-11-01). "Structural Phase Transitions in [(C 2 H 5 ) 4 N] 3 Sb 2 Br 9 and [(C 2 H 5 ) 4 N] 3 Bi 2 Br 9". Zeitschrift für Naturforschung A. 44 (11): 1102–1106. Bibcode:1989ZNatA..44.1102Z. doi:10.1515/zna-1989-1110. ISSN 1865-7109. S2CID 101200132.
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- ↑ Jacobson, Robert A.; Hackert, Marvin L.; Keiderling, Timothy A. (May 1971). "Crystal structure of tetraethylammonium hexabromoantimonate(V), (C2H5)4NSbBr6". Inorganic Chemistry. 10 (5): 1075–1078. doi:10.1021/ic50099a044. ISSN 0020-1669.
- ↑ N., Pislewski; J., Tritt-Goc; R., Jakubas. "Study on phase transitions and dynamics of n-propyl amine groups in (n-C3H7NH3)2SbBr5" (in Polish).
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(help) - ↑ Jakubas, R.; Bator, G.; Foulon, M.; Lefebvre, J.; Matuszewski, J. (1993-03-01). "Structural Phase Transitions in (n-C 3 H 7 NH 3 ) 2 SbBr 5". Zeitschrift für Naturforschung A. 48 (3): 529–534. Bibcode:1993ZNatA..48..529J. doi:10.1515/zna-1993-0314. ISSN 1865-7109. S2CID 102140570.
- ↑ Weslati, Najoua; Elgahami, Hanen; Hamdi, Mohamed; Oueslati, Abderrazek; Naïli, Houcine (June 2022). "Crystal structure, phase transition and electrical conductivity studies of [(C3H7)4N][SbBr4] compound". Journal of the Iranian Chemical Society. 19 (6): 2481–2493. doi:10.1007/s13738-021-02472-w. ISSN 1735-207X. S2CID 246235582.
- ↑ Tritt-Goc, By J.; Pislewski, N.; Goc, R.; Jakubas, H. PISLEWSKA and R. (November 1997). "Molecular motion in solid \[(CH3)2 CHNH3]2 BiBr5 and \[(CH3)2 CHNH3]2SbBr5 as studied by proton nuclear magnetic resonance". Molecular Physics. 92 (4): 687–692. Bibcode:1997MolPh..92..687T. doi:10.1080/002689797169961. ISSN 0026-8976.
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- ↑ Jakubas, R.; Jóźków, J.; Bator, G.; Zaleski, J.; Baran, J.; François, P. (December 1997). "Phase transitions in i-butylammonium halogenoantimonate(III) and bismuthate(III) crystals". Journal of Molecular Structure. 436–437: 315–325. Bibcode:1997JMoSt.436..315J. doi:10.1016/S0022-2860(97)00213-5.
- ↑ Chaabouni, S.; Kamoun, S.; Jaud, J. (March 1998). "Calorimetric Studies and Crystal Structure of [C2H10N2]5(Sb2Br11)2·4H2O". Materials Research Bulletin. 33 (3): 377–388. doi:10.1016/S0025-5408(97)00251-1.
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- ↑ Piecha, A.; Pietraszko, A.; Bator, G.; Jakubas, R. (May 2008). "Structural characterization and ferroelectric ordering in (C3N2H5)5Sb2Br11". Journal of Solid State Chemistry. 181 (5): 1155–1166. Bibcode:2008JSSCh.181.1155P. doi:10.1016/j.jssc.2008.02.029.
- ↑ Piecha, A.; Jakubas, R.; Kinzhybalo, V.; Medycki, W. (April 2012). "Crystal structure, dielectric properties and molecular motions of molecules in thiazolium halometalates(III): (C3H4NS)6M4Br18·2H2O (M=Sb, Bi)". Journal of Molecular Structure. 1013: 55–60. Bibcode:2012JMoSt1013...55P. doi:10.1016/j.molstruc.2012.01.014.
- ↑ McAfee, Elwin Ray (1970-11-01). "The crystal structure of quinolinium nonabromoantimonate (V), (C9H7NH)2SbVBr9 and the refinement of the molecular structure of beta-picoline-n-oxide fumaric acid adduct". doi:10.2172/4036792. OSTI 4036792.
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(help) - 1 2 3 Shentseva, Irina A.; Korobeynikov, Nikita A.; Usoltsev, Andrey N.; Gorokh, Igor D.; Novikov, Alexander S.; Korolkov, Ilya V.; Sokolov, Maxim N.; Adonin, Sergey A. (June 2023). "Haloantimonate(III) complexes with halogen-substituted quinolinium cations: structural features of non-covalent interactions in solid state". Polyhedron. 242: 116505. doi:10.1016/j.poly.2023.116505. S2CID 259796849.
- 1 2 3 Adonin, Sergey A.; Bondarenko, Mikhail A.; Novikov, Alexander S.; Abramov, Pavel A.; Plyusnin, Pavel E.; Sokolov, Maxim N.; Fedin, Vladimir P. (2019-10-14). "Antimony(V) Bromide and Polybromide Complexes with N-alkylated Quinolinium or Isoquinolinium Cations: Substituent-dependent Assembly of Polymeric Frameworks: Antimony(V) Bromide and Polybromide Complexes with N-alkylated Quinolinium or Isoquinolinium Cations: Substituent-dependent Assembly of Polymeric Fram". Zeitschrift für anorganische und allgemeine Chemie. 645 (18–19): 1141–1145. doi:10.1002/zaac.201900165. S2CID 204138784.
- ↑ Bukvetskiǐ B.V., Storozhuk T.V., Mirochnik A.G., Petrochenkova N.V., Karasev V.E. (2004). "CИНТЕЗ, КРИСТАЛЛИЧЕСКАЯ СТРУКТУРА И СПЕКТРАЛЬНОЛЮМИНЕСЦЕНТНЫЕ СВОЙСТВА КОМПЛЕКСНЫХ СОЕДИНЕНИЙ ГАЛОГЕНИДОВ СУРЬМЫ(III) С 6-МЕТИЛХИНОЛИНОМ" [SYNTHESIS, CRYSTAL STRUCTURE, AND LUMINESCENT PROPERTIES OF ANTIMONY(III) HALIDE COMPLEXES WITH 6-METHYLQUINOLINE]. Russian Journal of Inorganic Chemistry. 49 (1): 43–50.
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: CS1 maint: multiple names: authors list (link) - ↑ Ly, Kathy; May, Kathleen L.; Lough, Alan J.; Zhu, Jianfeng; Quail, J. Wilson; Gossage, Robert A. (February 2023). "Synthesis and structural characterisation of trivalent halidoantimonates and bismuthates of 2-methyl-2-benzoxazole (box): Reactivity and solid-state structural diversity within the [MX(6 – n)] [boxH](3 – n) series (M = Sb or Bi; X = Cl, Br, I; n = 0 or 1)". Journal of Solid State Chemistry. 318: 123653. Bibcode:2023JSSCh.31823653L. doi:10.1016/j.jssc.2022.123653.
- ↑ Lawton, Stephen L.; McAfee, Elwin Ray; Benson, James E.; Jacobson, Robert A. (December 1973). "Crystal structure of quinolinium hexabromoantimonate(V) tribromide, (C9H7NH)2SbVBr9". Inorganic Chemistry. 12 (12): 2939–2944. doi:10.1021/ic50130a040. ISSN 0020-1669.
- ↑ Lawton, Stephen L.; Jacobson, Robert A. (April 1971). "Crystal structure of quinuclidinium dodecarbromoantimon(III)antimonate(V)-2-dibromine, (C7H13NH)4Sb(III)Sb(V)Br12.2Br2". Inorganic Chemistry. 10 (4): 709–712. doi:10.1021/ic50098a010. ISSN 0020-1669.
- ↑ Taher, Marwa Ben; Chaari, Najla; Bechir, Mohamed Ben; Chaabouni, Slaheddine (April 2017). "X-ray diffraction, vibrational properties, and dielectric studies of 3-ammoniumpropyl imidazolium pentabromoantimonate (III)". Applied Physics A. 123 (4): 285. Bibcode:2017ApPhA.123..285T. doi:10.1007/s00339-017-0895-4. ISSN 0947-8396. S2CID 253852282.
- ↑ Chang, Jen-Hui; Doert, Thomas; Ruck, Michael (2016-12-01). "(H 3 O) 3 Sb 2 Br 9 : the first member of the M 3 E 2 X 9 structure family with oxonium cations". Acta Crystallographica Section C Structural Chemistry. 72 (12): 966–970. doi:10.1107/S2053229616017198. ISSN 2053-2296. PMID 27918298.
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- ↑ Czado, Wolfgang; Müller, Ulrich (December 2002). "Crystal structure of tetraphenylphosphonium hexabromoantimonate(V), P(C6H5)4SbBr6". Zeitschrift für Kristallographie - New Crystal Structures. 217 (JG): 337–338. doi:10.1524/ncrs.2002.217.jg.337. ISSN 2197-4578. S2CID 98343578.
- ↑ Fachbereich Biologie-Chemie, Universität Gh, D- Kassel, Wolfgang; Fachbereich Biologie-Chemie, Universität Gh, D- Kassel, Ulrich (1996-09-01). "Tetraphenylphosphonium-ikosioctabromooctaantimonat(III), (PPh 4 ) 4 Sb 8 Br 28 / Tetraphenylphosphonium Ikosioctabromooctaantimonate(III), (PPh 4 ) 4 Sb 8 Br 28". Zeitschrift für Naturforschung B. 51 (9): 1245–1247. doi:10.1515/znb-1996-0906. ISSN 1865-7117. S2CID 201092106.
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- ↑ Ephraim, Fritz; Weinberg, S. (November 1909). "Doppelhalogenide des drei-, vier- und fünfwertigen Antimons". Berichte der Deutschen Chemischen Gesellschaft. 42 (4): 4447–4456. doi:10.1002/cber.19090420441. ISSN 0365-9496.
- ↑ Chang, Jen-Hui; Doert, Thomas; Ruck, Michael (2020-09-25). "The crystal structures of α -Rb 7 Sb 3 Br 16 , α - and β -Tl 7 Bi 3 Br 16 and their relationship to close packings of spheres". Zeitschrift für Kristallographie - Crystalline Materials. 235 (8–9): 255–261. doi:10.1515/zkri-2020-0013. ISSN 2196-7105. S2CID 222005314.
- ↑ Mikhailov, Artem; Korobeynikov, Nikita; Usoltsev, Andrey; Adonin, Sergey A.; Kostin, Gennadiy A.; Schaniel, Dominik (2023). "Bismuth and antimony halometalates containing photoswitchable ruthenium nitrosyl complexes". Dalton Transactions. 52 (4): 919–927. doi:10.1039/D2DT03497B. ISSN 1477-9226. PMID 36594625. S2CID 254902411.
- ↑ Ruan, Hang; Guo, Zhongnan; Lin, Jiawei; Liu, Kunjie; Guo, Lingling; Chen, Xin; Zhao, Jing; Liu, Quanlin; Yuan, Wenxia (2021-10-04). "Structure and Optical Properties of Hybrid-Layered-Double Perovskites (C 8 H 20 N 2 ) 2 AgMBr 8 (M = In, Sb, and Bi)". Inorganic Chemistry. 60 (19): 14629–14635. doi:10.1021/acs.inorgchem.1c01669. ISSN 0020-1669. PMID 34523334. S2CID 237514261.
- ↑ Zhang, Jian; Yang, Ying; Deng, Hui; Farooq, Umar; Yang, Xiaokun; Khan, Jahangeer; Tang, Jiang; Song, Haisheng (2017-09-26). "High Quantum Yield Blue Emission from Lead-Free Inorganic Antimony Halide Perovskite Colloidal Quantum Dots". ACS Nano. 11 (9): 9294–9302. doi:10.1021/acsnano.7b04683. ISSN 1936-0851. PMID 28880532.
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