Rational Design of Porous Coordination Polymers Based on Bis(phosphine)MCl2 Complexes That Exhibit High-Temperature H2 Sorption and Chemical Reactivity

2013 ◽  
Vol 135 (43) ◽  
pp. 16038-16041 ◽  
Author(s):  
Alisha M. Bohnsack ◽  
Ilich A. Ibarra ◽  
Vladimir I. Bakhmutov ◽  
Vincent M. Lynch ◽  
Simon M. Humphrey
2010 ◽  
Vol 16 (34) ◽  
pp. 10348-10356 ◽  
Author(s):  
Danil N. Dybtsev ◽  
Maxim P. Yutkin ◽  
Denis G. Samsonenko ◽  
Vladimir P. Fedin ◽  
Alexey L. Nuzhdin ◽  
...  

2012 ◽  
Vol 85 (2) ◽  
pp. 405-416 ◽  
Author(s):  
Yue-Biao Zhang ◽  
Jie-Peng Zhang

While isotropic metal–carboxylate clusters as secondary building blocks have enabled the rational design of porous coordination polymers (PCPs) with predictable topologies, augmented metal–carboxylate–pyridyl clusters can be used as anisotropic secondary building blocks to facilitate the construction of higher-connectivity frameworks and control over structural directionality in self-assembly.


2013 ◽  
Vol 3 (2) ◽  
pp. 144-160 ◽  
Author(s):  
Sergey Kolotilov ◽  
Mikhail Kiskin ◽  
Igor Eremenko ◽  
Vladimir Novotortsev

2021 ◽  
Author(s):  
Meng-Hua Li ◽  
Ming-Hua You ◽  
Mei-Jin Lin

The incorporation of photochromic moieties into porous coordination polymers is of particular interest due to it can endow them various switchable functions in the electrical conductivity, luminescence, and magnetism. In...


2021 ◽  
Author(s):  
Yifan Gu ◽  
Jia‐Jia Zheng ◽  
Ken‐ichi Otake ◽  
Mohana Shivanna ◽  
Shigeyoshi Sakaki ◽  
...  

Author(s):  
Verónica G. Vegas ◽  
Ana Latorre ◽  
María Luisa Marcos ◽  
Carlos J. Gómez-García ◽  
Óscar Castillo ◽  
...  

2003 ◽  
Vol 787 ◽  
Author(s):  
John D. Bass ◽  
Sandra L. Anderson ◽  
Alexander Katz

AbstractThe effect of chemical environment surrounding a synthetic heterogeneous catalyst active site is investigated using the hydrophilic imprinting of silica. Two model reaction systems have been used for this study: (i) Knoevenagel condensation of 3-nitrobenzaldehyde and malononitrile and (ii) Suzuki coupling of bromobenzene and phenylboronic acid. Using a catalyst in which isolated imprinted amines are surrounded by an acidic silanol-rich environment led to rate accelerations of over 120-fold relative to catalysts in which the amines are surrounded by a hydrophobic environment consisting of trimethylsilyl functional groups for system (i). This result parallels our previous study on the effect of the outer sphere composition on rate acceleration of Knoevenagel reactions using isophthalaldehyde as the aldehyde reactant. We also extended our method for the hydrophilic imprinting of bulk silica to organometallic systems, by successfully synthesizing a tethered palladium complex within the imprinted pocket. This material was used as an active catalyst for (ii). Our results show that a hydrophobic framework environment results in higher initial turnover frequencies than an acidic silanol-rich framework for the Suzuki coupling reaction of bromobenzene and phenylboronic acid, albeit with a lower overall effect than observed in the Knoevenagel system (i). Altogether, these results demonstrate the control of chemical reactivity via the rational design of the outer sphere using an imprinting approach.


2010 ◽  
Vol 171 (1) ◽  
pp. 108-122 ◽  
Author(s):  
G. F. Kessinger ◽  
A. R. Jurgensen ◽  
D. M. Missimer ◽  
J. S. Morrell

EnergyChem ◽  
2021 ◽  
pp. 100067
Author(s):  
Nibedita Behera ◽  
Jingui Duan ◽  
Wanqin Jin ◽  
Susumu Kitagawa

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