Home > Publications database > Group 13 Metal Carboxylates: Using Molecular Clusters As Hybrid Building Units in a MIL-53 Type Framework > print |
001 | 207237 | ||
005 | 20250730145731.0 | ||
024 | 7 | _ | |a 10.1021/cg501189n |2 doi |
024 | 7 | _ | |a 1528-7483 |2 ISSN |
024 | 7 | _ | |a 1528-7505 |2 ISSN |
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100 | 1 | _ | |a Wharmby, Michael |0 P:(DE-H253)PIP1016411 |b 0 |e Corresponding Author |
245 | _ | _ | |a Group 13 Metal Carboxylates: Using Molecular Clusters As Hybrid Building Units in a MIL-53 Type Framework |
260 | _ | _ | |a Washington, DC |c 2014 |b ACS Publ. |
336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
336 | 7 | _ | |a article |2 DRIVER |
336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1432201283_6327 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
500 | _ | _ | |a (c) American Chemical Society. Post referee full text in progress. Embargo for full text 1 year from August 20, 2014. |
520 | _ | _ | |a Systematic investigation of the reactions of the system AlCl3·6H2O/pyridine-2,4,6-tricarboxylic acid (H3PTC)/pyridine in water yielded two new compounds, both containing the dimeric {AlPTC(μ-OH)(H2O)}22– unit. With long reaction times, the framework compound [Al(μ-OH){AlPTC(μ-OH)(H2O)}2]·2H2O (CAU-16, compound 1) is obtained, the first example of a framework compound with a metal–organic cluster linker, and bearing the MIL-53 network. Although the compound does not breathe, as other MIL-53 compounds do, it has a maximum uptake of CO2 of 1.76(2) mmol g–1 at 196 K. With shorter reaction times, the molecular compound {Al(HPTC)(μ-OH)(H2O)}2 (2) was prepared, leading to the proposal of a crystallization scheme for the Al3+-pyridine-2,4,6,-tricarboxylic acid system. To determine whether further framework compounds bearing hybrid metal cluster linkers could be prepared, systematic high-throughput investigations of pyridine-2,4,6-tricarboxylic acid in water with Ga3+ and In3+ were undertaken. These yielded two chain-type compounds, GaPTC(H2O)2 (3) and InPTC(H2O)2 (4), with different coordination chemistries. Optimized syntheses for compounds 1, 2, and 4 are reported. |
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773 | _ | _ | |a 10.1021/cg501189n |g Vol. 14, no. 10, p. 5310 - 5317 |0 PERI:(DE-600)2048329-6 |n 10 |p 5310 - 5317 |t Crystal growth & design |v 14 |y 2014 |x 1528-7483 |
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