TY - JOUR
T1 - Microsphere Assemblies via Phosphonate Monoester Coordination Chemistry
AU - Bladek, Kamila J.
AU - Reid, Margaret E.
AU - Nishihara, Hirotomo
AU - Akhtar, Farid
AU - Gelfand, Benjamin S.
AU - Shimizu, George K.H.
N1 - Funding Information:
We thank the Natural Sciences and Engineering Research Council (NSERC) of Canada for CGS-D Awards for K.J.B. and B.S.G. and the CREATE Carbon Capture Initiative. The authors thank Leonardo Pelcastre for help with nano-indentation measurements.
Publisher Copyright:
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/2/1
Y1 - 2018/2/1
N2 - By complexing a bent phosphonate monoester ligand with cobalt(II), coupled with in situ ester hydrolysis, coordination microspheres (CALS=CALgary Sphere) are formed whereas the use of the phosphonic acid directly resulted in a sheet-like structure. Manipulation of the synthetic conditions gave spheres with different sizes, mechanical stabilities, and porosities. Time-dependent studies determined that the sphere formation likely occurred through the formation of a Co2+ and ligand chain that propagates in three dimensions through different sets of interactions. The relative rates of these assembly processes versus annealing by ester hydrolysis and metal dehydration determine the growth of the microspheres. Hardness testing by nanoindentation is carried out on the spheres and sheets. Notably, no templates or capping agents are employed, the growth of the spheres is intrinsic to the ligand geometry and the coordination chemistry of cobalt(II) and the phosphonate monoester.
AB - By complexing a bent phosphonate monoester ligand with cobalt(II), coupled with in situ ester hydrolysis, coordination microspheres (CALS=CALgary Sphere) are formed whereas the use of the phosphonic acid directly resulted in a sheet-like structure. Manipulation of the synthetic conditions gave spheres with different sizes, mechanical stabilities, and porosities. Time-dependent studies determined that the sphere formation likely occurred through the formation of a Co2+ and ligand chain that propagates in three dimensions through different sets of interactions. The relative rates of these assembly processes versus annealing by ester hydrolysis and metal dehydration determine the growth of the microspheres. Hardness testing by nanoindentation is carried out on the spheres and sheets. Notably, no templates or capping agents are employed, the growth of the spheres is intrinsic to the ligand geometry and the coordination chemistry of cobalt(II) and the phosphonate monoester.
KW - cobalt
KW - metal–organic frameworks
KW - microstructure
KW - nanoindentation
KW - phosphonate monoester
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U2 - 10.1002/chem.201705985
DO - 10.1002/chem.201705985
M3 - Article
C2 - 29336090
AN - SCOPUS:85040689592
SN - 0947-6539
VL - 24
SP - 1533
EP - 1538
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 7
ER -