TY - JOUR
T1 - Melt-Quenched Glasses of Metal–Organic Frameworks
AU - Bennett, Thomas D.
AU - Yue, Yuanzheng
AU - Li, Peng
AU - Qiao, Ang
AU - Tao, Haizheng
AU - Greaves, Neville G.
AU - Richards, Tom
AU - Lampronti, Giulio I.
AU - Redfern, Simon A. T.
AU - Blanc, Frédéric
AU - Farha, Omar K.
AU - Hupp, Joseph T.
AU - Cheetham, Anthony K.
AU - Keen, David A.
N1 - Funding Information:
T.D.B. would like to thank Trinity Hall (University of Cambridge) for funding. We thank Diamond Light Source for access to beamline B18 (SP14249-1) that contributed to the results presented here. We thank Dr. Giannantonio Cibin and Dr. Stephen Parry for their assistance with the EXAFS measurements. F.B. thanks EPSRC (grant EP/M00869X/1) and the University of Liverpool for funding. O.K.F. gratefully acknowledges funding from the Army Research Office (project number W911NF-13-1-0229). S.A.T.R. is grateful for funding from the Natural Environment Research Council.
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/3/16
Y1 - 2016/3/16
N2 - Crystalline solids dominate the field of metal–organic frameworks (MOFs), with access to the liquid and glass states of matter usually prohibited by relatively low temperatures of thermal decomposition. In this work, we give due consideration to framework chemistry and topology to expand the phenomenon of the melting of 3D MOFs, linking crystal chemistry to framework melting temperature and kinetic fragility of the glass-forming liquids. Here we show that melting temperatures can be lowered by altering the chemistry of the crystalline MOF state, which provides a route to facilitate the melting of other MOFs. The glasses formed upon vitrification are chemically and structurally distinct from the three other existing categories of melt-quenched glasses (inorganic nonmetallic, organic, and metallic), and retain the basic metal–ligand connectivity of crystalline MOFs, which connects their mechanical properties to their starting chemical composition. The transfer of functionality from crystal to glass points toward new routes to tunable, functional hybrid glasses.
AB - Crystalline solids dominate the field of metal–organic frameworks (MOFs), with access to the liquid and glass states of matter usually prohibited by relatively low temperatures of thermal decomposition. In this work, we give due consideration to framework chemistry and topology to expand the phenomenon of the melting of 3D MOFs, linking crystal chemistry to framework melting temperature and kinetic fragility of the glass-forming liquids. Here we show that melting temperatures can be lowered by altering the chemistry of the crystalline MOF state, which provides a route to facilitate the melting of other MOFs. The glasses formed upon vitrification are chemically and structurally distinct from the three other existing categories of melt-quenched glasses (inorganic nonmetallic, organic, and metallic), and retain the basic metal–ligand connectivity of crystalline MOFs, which connects their mechanical properties to their starting chemical composition. The transfer of functionality from crystal to glass points toward new routes to tunable, functional hybrid glasses.
UR - http://www.scopus.com/inward/record.url?scp=84961242640&partnerID=8YFLogxK
U2 - 10.1021/jacs.5b13220
DO - 10.1021/jacs.5b13220
M3 - Article
C2 - 26885940
SN - 0002-7863
VL - 138
SP - 3484
EP - 3492
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 10
ER -