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Vapor-phase synthesis of low-valent metal-organic frameworks from metal carbonyl synthons
被引:4
|作者:
Andersen, Carl Emil
[1
]
McPherson, James Neill
[1
]
Gimenez-Marques, Monica
[2
]
Li, Jingguo
[3
]
Kubus, Mariusz
[1
]
Ito, Sho
[4
]
Goeb, Christian R. R.
[5
]
Ott, Sascha
[3
]
Larsen, Rene Wugt
[1
]
Espallargas, Guillermo Minguez
[2
]
Pedersen, Kasper S. S.
[1
]
机构:
[1] Tech Univ Denmark, Dept Chem, Kemitorvet 207, DK-2800 Lyngby, Denmark
[2] Univ Valencia, Inst Ciencia Mol ICMol, Paterna 46980, Valencia, Spain
[3] Uppsala Univ, Dept Chem, Angstrom Lab, S-75120 Uppsala, Sweden
[4] Rigaku Corp, 3-9-12 Matsubara Cho, Akishima, Tokyo 1968666, Japan
[5] Rigaku Europe SE, Hugenottenallee 167, D-63263 Neu Isenburg, Germany
关键词:
ELECTROCATALYTIC REDUCTION;
LAYER DEPOSITION;
THIN-FILMS;
CO2;
COMPLEXES;
D O I:
10.1039/d3tc02088f
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
Incorporating low-valent metals as nodes in metal-organic frameworks (MOFs) is orthogonal to the commonly accepted strategy to robust and porous structures. The electronic structures of low-valent metals are chemically unique and have driven the successes of organometallic chemistry. The translation of these properties into MOFs is largely impeded by the lack of generalizable synthetic approaches. Metal carbonyls are bona fide low-valent and volatile synthons, which, by partial chemical substitution may tether ditopic ligands into MOF architectures. We herein demonstrate the formation of CO2 adsorbing MOFs from the direct vapor-phase substitution of CO by ditopic 4,4 & PRIME;-bipyridine at Mo(0) and W(0) centers, which allows facile coating of low-valent MOFs onto substrates such as indium tin oxide. We envisage this strategy could be generalized to a multitude of mono- and polynuclear metal carbonyls, paralleling the diversity of conventional MOFs.
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页码:11460 / 11465
页数:6
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