Hydrothermal synthesis of Group 13 metal trifluoride complexes with neutral N-donor ligands
The reactions of the hydrated Group 13 fluorides, MF3·3H2O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline under hydrothermal conditions (180 °C/15 h) produced high yields of the complexes [MF3(terpy)]·3H2O, [MF3(bipy)(OH2)]·2H2O and [MF...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 44; no. 20; pp. 9569 - 9580 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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England
28.05.2015
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Abstract | The reactions of the hydrated Group 13 fluorides, MF3·3H2O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline under hydrothermal conditions (180 °C/15 h) produced high yields of the complexes [MF3(terpy)]·3H2O, [MF3(bipy)(OH2)]·2H2O and [MF3(phen)(OH2)]. X-Ray crystal structures of [M'F3(terpy)]·3H2O (M' = Al or Ga), [M'F3(bipy)(OH2)]·2H2O and [GaF3(phen)(OH2)] show that all of them contain distorted octahedral geometries at the metal with mer-trifluoride coordination. Extensive H-bonding (FH-OH) links the molecules. The complexes have been further characterised by microanalysis, IR, (1)H, (19)F{(1)H} and (27)Al NMR spectroscopy. In contrast, reactions of the trifluorides with the acyclic triamine, N,N,N',N',N''-pentamethyldiethylenetriamine, under similar hydrothermal conditions results in cleavage of the triamine and ring-closure to form the 1,1,4-trimethylpiperazinium cation, [⊂Me2N(CH2)2NMe(CH2)2](+), with fluorometallate anions, and confirmed by X-ray analysis of [⊂Me2N(CH2)2NMe(CH2)2]2[Al2F8(OH2)2]·2H2O. The strongly H-bonded [GaF3(terpy)]·3H2O was also obtained by Cl/F exchange from [GaCl3(terpy)] and [NBu4]F or [K(2,2,2-crypt)]F. Crystallisation of a mixture of [NH4][PF6] and [GaF3(terpy)]·3H2O from aqueous solution produced the edge-bridged cationic complex, [{Ga(terpy)F}2(μ-F)2][PF6]2. The synthesis of the more sterically bulky [GaCl3((t)Bu3-terpy)] ((t)Bu3-terpy = 4,4'4''-tris-(t)Bu-2,2':6',2''-terpyridyl) and the crystal structure of [GaCl2((t)Bu3-terpy)][GaCl4], which contains a trigonal bipyramidal cation, are also reported. |
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AbstractList | The reactions of the hydrated Group 13 fluorides, MF3·3H2O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline under hydrothermal conditions (180 °C/15 h) produced high yields of the complexes [MF3(terpy)]·3H2O, [MF3(bipy)(OH2)]·2H2O and [MF3(phen)(OH2)]. X-Ray crystal structures of [M'F3(terpy)]·3H2O (M' = Al or Ga), [M'F3(bipy)(OH2)]·2H2O and [GaF3(phen)(OH2)] show that all of them contain distorted octahedral geometries at the metal with mer-trifluoride coordination. Extensive H-bonding (FH-OH) links the molecules. The complexes have been further characterised by microanalysis, IR, (1)H, (19)F{(1)H} and (27)Al NMR spectroscopy. In contrast, reactions of the trifluorides with the acyclic triamine, N,N,N',N',N''-pentamethyldiethylenetriamine, under similar hydrothermal conditions results in cleavage of the triamine and ring-closure to form the 1,1,4-trimethylpiperazinium cation, [⊂Me2N(CH2)2NMe(CH2)2](+), with fluorometallate anions, and confirmed by X-ray analysis of [⊂Me2N(CH2)2NMe(CH2)2]2[Al2F8(OH2)2]·2H2O. The strongly H-bonded [GaF3(terpy)]·3H2O was also obtained by Cl/F exchange from [GaCl3(terpy)] and [NBu4]F or [K(2,2,2-crypt)]F. Crystallisation of a mixture of [NH4][PF6] and [GaF3(terpy)]·3H2O from aqueous solution produced the edge-bridged cationic complex, [{Ga(terpy)F}2(μ-F)2][PF6]2. The synthesis of the more sterically bulky [GaCl3((t)Bu3-terpy)] ((t)Bu3-terpy = 4,4'4''-tris-(t)Bu-2,2':6',2''-terpyridyl) and the crystal structure of [GaCl2((t)Bu3-terpy)][GaCl4], which contains a trigonal bipyramidal cation, are also reported. The reactions of the hydrated Group 13 fluorides, MF 3 ·3H 2 O (M = Al, Ga or In) with 2,2′:6′,2′′-terpyridyl, 2,2′-bipyridyl or 1,10-phenanthroline under hydrothermal conditions (180 °C/15 h) produced high yields of the complexes [MF 3 (terpy)]·3H 2 O, [MF 3 (bipy)(OH 2 )]·2H 2 O and [MF 3 (phen)(OH 2 )]. X-Ray crystal structures of [M′F 3 (terpy)]·3H 2 O (M′ = Al or Ga), [M′F 3 (bipy)(OH 2 )]·2H 2 O and [GaF 3 (phen)(OH 2 )] show that all of them contain distorted octahedral geometries at the metal with mer -trifluoride coordination. Extensive H-bonding (F⋯H–OH) links the molecules. The complexes have been further characterised by microanalysis, IR, 1 H, 19 F{ 1 H} and 27 Al NMR spectroscopy. In contrast, reactions of the trifluorides with the acyclic triamine, N , N , N ′, N ′, N ′′-pentamethyldiethylenetriamine, under similar hydrothermal conditions results in cleavage of the triamine and ring-closure to form the 1,1,4-trimethylpiperazinium cation, [⊂Me 2 N(CH 2 ) 2 NMe(CH 2 ) 2 ] + , with fluorometallate anions, and confirmed by X-ray analysis of [⊂Me 2 N(CH 2 ) 2 NMe(CH 2 ) 2 ] 2 [Al 2 F 8 (OH 2 ) 2 ]·2H 2 O. The strongly H-bonded [GaF 3 (terpy)]·3H 2 O was also obtained by Cl/F exchange from [GaCl 3 (terpy)] and [NBu 4 ]F or [K(2,2,2-crypt)]F. Crystallisation of a mixture of [NH 4 ][PF 6 ] and [GaF 3 (terpy)]·3H 2 O from aqueous solution produced the edge-bridged cationic complex, [{Ga(terpy)F} 2 (μ-F) 2 ][PF 6 ] 2 . The synthesis of the more sterically bulky [GaCl 3 ( t Bu 3 -terpy)] ( t Bu 3 -terpy = 4,4′4′′-tris- t Bu-2,2′:6′,2′′-terpyridyl) and the crystal structure of [GaCl 2 ( t Bu 3 -terpy)][GaCl 4 ], which contains a trigonal bipyramidal cation, are also reported. The reactions of the hydrated Group 13 fluorides, MF sub(3).3H sub(2)O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline under hydrothermal conditions (180 degree C/15 h) produced high yields of the complexes [MF sub(3)(terpy)].3H sub(2)O, [MF sub(3)(bipy)(OH sub(2))].2H sub(2)O and [MF sub(3)(phen)(OH sub(2))]. X-Ray crystal structures of [M'F sub(3)(terpy)].3H sub(2)O (M' = Al or Ga), [M'F sub(3)(bipy)(OH sub(2))].2H sub(2)O and [GaF sub(3)(phen)(OH sub(2))] show that all of them contain distorted octahedral geometries at the metal with mer-trifluoride coordination. Extensive H-bonding (F...H-OH) links the molecules. The complexes have been further characterised by microanalysis, IR, super(1)H, super(19)F{ super(1)H} and super(27)Al NMR spectroscopy. In contrast, reactions of the trifluorides with the acyclic triamine, N,N,N',N',N''-pentamet hyldiethylenetriamine, under similar hydrothermal conditions results in cleavage of the triamine and ring-closure to form the 1,1,4-trimethylpiperazinium cation, [ sub(Me) sub(2)N(CH sub(2)) sub(2)NMe(CH sub(2)) sub(2)] super(+), with fluorometallate anions, and confirmed by X-ray analysis of [ sub(Me) sub(2)N(CH sub(2)) sub(2)NMe(CH sub(2)) sub(2)] sub(2)[Al sub(2)F sub(8)(OH sub(2) sub(2)].2H sub(2)O. The strongly H-bonded [GaF sub(3)(terpy)].3H sub(2)O was also obtained by Cl/F exchange from [GaCl sub(3)(terpy)] and [NBu sub(4)]F or [K(2,2,2-crypt)]F. Crystallisation of a mixture of [NH sub(4)][PF sub(6)] and [GaF sub(3)(terpy)].3H sub(2)O from aqueous solution produced the edge-bridged cationic complex, [{Ga(terpy)F} sub(2)( mu -F) sub(2)][PF sub(6)] sub(2). The synthesis of the more sterically bulky [GaCl sub(3)( super(t)Bu sub(3)-terpy)] ( super(t)Bu sub(3)-terpy = 4,4'4''-tris- super(t) Bu-2,2':6',2''-terpyridyl) and the crystal structure of [GaCl sub(2)( super(t)Bu sub(3)-terpy)][GaCl sub(4)], which contains a trigonal bipyramidal cation, are also reported. |
Author | Monzittu, Francesco M McRobbie, Graeme Reid, Gillian Sanderson, George Luthra, Sajinder K Zhang, Wenjian Palmer, Jazmyn Bhalla, Rajiv Levason, William |
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CitedBy_id | crossref_primary_10_1039_D3QI01245J crossref_primary_10_1021_acs_organomet_8b00265 crossref_primary_10_1007_s11172_015_1188_8 crossref_primary_10_1016_j_ccr_2019_04_005 crossref_primary_10_1515_revic_2017_0010 crossref_primary_10_1039_C8DT00480C crossref_primary_10_1039_C7DT03709K crossref_primary_10_3390_inorganics10080107 crossref_primary_10_1016_j_poly_2015_12_032 crossref_primary_10_3390_cryst13060885 crossref_primary_10_1016_j_poly_2021_115367 crossref_primary_10_1021_acs_inorgchem_9b02592 crossref_primary_10_1515_revic_2015_0019 crossref_primary_10_1039_C8DT03696A |
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Snippet | The reactions of the hydrated Group 13 fluorides, MF3·3H2O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline under... The reactions of the hydrated Group 13 fluorides, MF 3 ·3H 2 O (M = Al, Ga or In) with 2,2′:6′,2′′-terpyridyl, 2,2′-bipyridyl or 1,10-phenanthroline under... The reactions of the hydrated Group 13 fluorides, MF sub(3).3H sub(2)O (M = Al, Ga or In) with 2,2':6',2''-terpyridyl, 2,2'-bipyridyl or 1,10-phenanthroline... |
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SubjectTerms | Aluminum Cations Coordination compounds Crystal structure Crystallization Gallium Synthesis (chemistry) X-rays |
Title | Hydrothermal synthesis of Group 13 metal trifluoride complexes with neutral N-donor ligands |
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