Soluble imidazolium-functionalized coordination cages for efficient homogeneous catalysis of CO2 cycloaddition reactions

2021 ◽  
Author(s):  
Hui-Ying Tong ◽  
Jun Liang ◽  
Qiu-Jin Wu ◽  
Yu-Huang Zou ◽  
Yuan-Biao Huang ◽  
...  

The soluble metal–organic cage ImBDC-Co can be employed as a homogeneous catalyst for the CO2 cycloaddition reaction, and shows higher catalytic activity than its heterogeneous counterparts. Moreover, the soluble cage can realize recovery and reuse without activity loss.

2017 ◽  
Vol 5 (30) ◽  
pp. 15961-15969 ◽  
Author(s):  
Robin Babu ◽  
Roshith Roshan ◽  
Yeongrok Gim ◽  
Yun Hee Jang ◽  
Jintu Francis Kurisingal ◽  
...  

The correlation between dimensionality and active sites on deciding the catalytic performance of an MOF catalyst in CO2–epoxide cycloaddition reactions has been studied.


RSC Advances ◽  
2015 ◽  
Vol 5 (84) ◽  
pp. 69006-69009 ◽  
Author(s):  
Zhiyuan Huo ◽  
Jipeng Guo ◽  
Jingkun Lu ◽  
Qiaofei Xu ◽  
Pengtao Ma ◽  
...  

A nona-vacant Keggin-type tricarbonyl rhenium derivative {[PMo3O16][Re(CO)3]4}5− was synthesized and its frontier orbitals were computed. Interestingly, it showed good catalytic activity for the CO2 cycloaddition reaction.


2017 ◽  
Vol 41 (16) ◽  
pp. 8166-8177 ◽  
Author(s):  
Poonam Rani ◽  
Rajendra Srivastava

Optimum acidity and basicity of amine functionalized metal organic frameworks are important for condensation and cycloaddition reactions.


Author(s):  
Rong Cao ◽  
Fa-Xue Ma ◽  
Fu-Qi Mi ◽  
Meng-Jiao Sun ◽  
Tao Huang ◽  
...  

A three-dimensional (3D) metal-organic framework constructed from unprecedented Zn9O2(OH)2(pyz)12 (pyz = pyrazolate) clusters and Ni(salen)-derived linkers was reported. The MOF exhibits high catalytic activity for CO2 cycloaddition reactions with excellent...


2021 ◽  
Author(s):  
Aishanee Sur ◽  
Nicholas Jernigan ◽  
David Powers

The development of homogeneous catalysis is enabled by the availability of a rich toolkit of kinetics experiments, such as the Hg-drop test, that differentiate catalytic activity at ligand-supported metal complexes from potential heterogeneous catalysts derived from decomposition of molecular species. Metal-organic frameworks (MOFs) have garnered significant attention as platforms for catalysis at site-isolated, interstitial catalyst sights. Unlike homogeneous catalysis, relatively few strategies have been advanced to evaluate the origin of catalytic activity in MOF-promoted reactions. Many of the MOFs that have been examined as potential catalysts are comprised of molecular constituents that represent viable catalysts in the absence of the extended MOF lattice, and thus interfacial sites and leached homogeneous species represent potential sources of catalyst activity. Here, we demonstrate that analysis of deuterium kinetic isotope effects (KIEs) and olefin epoxidation diastereoselectivity provides direct probes of the origin of catalytic activity in MOF-promoted oxidation reactions. These analyses support direct involvement of lattice-based Fe sites in the turnover-limiting step of C–H activation with Fe-MOF-74-based materials (i.e., the MOF functions as a bona fide catalyst) and evidence that Cu2-based MOF MIL-125-Cu2O2 functions as a solid-state initiator for solution-phase oxidation chemistry and is not involved in the turnover limiting step (i.e., the MOF does not function as a catalyst). We anticipate that the simple experiments described here will provide a valuable tool for clarifying the role of MOFs in C–H oxidation reactions.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mohammad Hossein Abdollahi-Basir ◽  
Boshra Mirhosseini-Eshkevari ◽  
Farzad Zamani ◽  
Mohammad Ali Ghasemzadeh

AbstractA one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterized by XRD, FE-SEM, EDX, FT-IR, TGA, BET, and TEM exhibited outstanding catalytic activity for the preparation of a range of pharmaceutically important tetrazolo[1,5-a]pyrimidine-6-carbonitriles with good to excellent yields in short reaction time.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3525
Author(s):  
Leslie Trigoura ◽  
Yalan Xing ◽  
Bhanu P. S. Chauhan

In this review, we present an assessment of recent advances in alkyne functionalization reactions, classified according to different classes of recyclable catalysts. In this work, we have incorporated and reviewed the activity and selectivity of recyclable catalytic systems such as polysiloxane-encapsulated novel metal nanoparticle-based catalysts, silica–copper-supported nanocatalysts, graphitic carbon-supported nanocatalysts, metal organic framework (MOF) catalysts, porous organic framework (POP) catalysts, bio-material-supported catalysts, and metal/solvent free recyclable catalysts. In addition, several alkyne functionalization reactions have been elucidated to demonstrate the success and efficiency of recyclable catalysts. In addition, this review also provides the fundamental knowledge required for utilization of green catalysts, which can combine the advantageous features of both homogeneous (catalyst modulation) and heterogeneous (catalyst recycling) catalysis.


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