TCNQ Dianion-Based Coordination Polymer Whose Open Framework Shows Charge-Transfer Type Guest Inclusion

2006 ◽  
Vol 128 (51) ◽  
pp. 16416-16417 ◽  
Author(s):  
Satoru Shimomura ◽  
Ryotaro Matsuda ◽  
Takashi Tsujino ◽  
Takashi Kawamura ◽  
Susumu Kitagawa

CrystEngComm ◽  
2020 ◽  
Vol 22 (40) ◽  
pp. 6612-6619
Author(s):  
Junling Chen ◽  
Bo Li ◽  
Zhenzhen Shi ◽  
Cheng He ◽  
Chunying Duan ◽  
...  

This work revealed that the synergy of microporous channels and convergent arrangements of halogen bonding and charge-transfer interaction sites within coordination polymers facilitated the iodine adsorption process.



2015 ◽  
Vol 17 (8) ◽  
pp. 4228-4233 ◽  
Author(s):  
Akira Takahashi ◽  
Nobutsugu Minami ◽  
Hisashi Tanaka ◽  
Kiwamu Sue ◽  
Kimitaka Minami ◽  
...  

An efficient preparation of size-controlled nanoparticles of an open framework coordination polymer.



2014 ◽  
Vol 53 (28) ◽  
pp. 7188-7191 ◽  
Author(s):  
Li Wei ◽  
Qi Wei ◽  
Zhi‐En Lin ◽  
Qin Meng ◽  
Huan He ◽  
...  


2011 ◽  
Vol 40 (11) ◽  
pp. 2422 ◽  
Author(s):  
Jérôme Lhoste ◽  
Natacha Henry ◽  
Pascal Roussel ◽  
Thierry Loiseau ◽  
Francis Abraham


2016 ◽  
Vol 128 (20) ◽  
pp. 6151-6154 ◽  
Author(s):  
Kuirun Zhang ◽  
Soonchul Kang ◽  
Zi-shuo Yao ◽  
Kazusa Nakamura ◽  
Takashi Yamamoto ◽  
...  


2020 ◽  
Vol 76 (5) ◽  
pp. 375-380
Author(s):  
Wen-Tong Chen

A novel manganese(III)–porphyrin complex, namely, catena-poly[[chloridomanganese(III)]-μ2-5,10,15,20-tetrakis(pyridin-3-yl)-21H,23H-porphinato(2−)-κ5 N 21,N 22,N 23,N 24:N 5], [MnCl(C40H24N8)] n , 1, was prepared by the hydrothermal reaction of manganese chloride with 5,10,15,20-tetrakis(pyridin-3-yl)-21H,23H-porphine. The crystal structure was determined by single-crystal X-ray diffraction. The porphyrin macrocycle exhibits a saddle-like distortion geometry. The MnIII atom has a six-coordination geometry. Each porphyrin unit links to two neighbouring units to yield a one-dimensional coordination polymer. These chains are further interlinked by hydrogen bonds to form a two-dimensional network. The complex shows red photoluminescence emission bands in ethanol solution, which can be attributed to ligand-to-ligand charge transfer (LLCT) accompanied by partial metal-to-ligand charge transfer (MLCT), as revealed by TDDFT calculations.



2014 ◽  
Vol 126 (28) ◽  
pp. 7316-7319 ◽  
Author(s):  
Li Wei ◽  
Qi Wei ◽  
Zhi‐En Lin ◽  
Qin Meng ◽  
Huan He ◽  
...  


2020 ◽  
Author(s):  
Parul Verma ◽  
Pallavi Sarkar ◽  
Ashish Singh ◽  
Swapan Pati ◽  
Tapas Maji

Abstract The much-needed renewable alternatives to fossil fuel can be achieved efficiently and sustainably by converting solar energy to solar fuels via hydrogen generation from water or CO2 reduction. In this regard, a soft processable metal-organic hybrid semiconducting material has been developed and studied for photocatalytic activity towards H2 production and CO2 reduction to CO and CH4 under visible light and direct sunlight irradiation. A tetrapodal low molecular weight gelator is synthesized by integrating tetrathiafulvalene and terpyridine through amide linkage (TPY-TTF). The TPY-TTF acts as a linker and by self-assembly with ZnII results in a charge-transfer (CT) coordination polymer gel (CPG); Zn-TPY-TTF. The Zn-TPY-TTF shows impressive photocatalytic activity towards H2 production (rate = 530 μmol g-1h-1) and CO2 reduction to CO (rate = 438 μmol g-1h-1, selectivity >99%) regulated by charge-transfer interaction. Furthermore, in-situ stabilization of Pt nanoparticles to CPG (Pt@Zn-TPY-TTF) exhibits remarkably enhanced H2 evolution (rate =14727 μmol g-1h-1). Importantly, Pt@Zn-TPY-TTF modulate the CO2 reduction from CO to CH4 (rate = 292 μmol g-1h-1, selectivity >97%). Real-time CO2 reduction reaction is monitored by in-situ DRIFT study and subsequent plausible mechanism is derived computationally. The photocatalytic activity of Zn-TPY-TTF and Pt@Zn-TPY-TTF composite was also examined under sunlight that display excellent H2 evolution and CO2 reduction.



2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Parul Verma ◽  
Ashish Singh ◽  
Faruk Ahamed Rahimi ◽  
Pallavi Sarkar ◽  
Sukhendu Nath ◽  
...  

AbstractThe much-needed renewable alternatives to fossil fuel can be achieved efficiently and sustainably by converting solar energy to fuels via hydrogen generation from water or CO2 reduction. Herein, a soft processable metal-organic hybrid material is developed and studied for photocatalytic activity towards H2 production and CO2 reduction to CO and CH4 under visible light as well as direct sunlight irradiation. A tetrapodal low molecular weight gelator (LMWG) is synthesized by integrating tetrathiafulvalene (TTF) and terpyridine (TPY) derivatives through amide linkages and results in TPY-TTF LMWG. The TPY-TTF LMWG acts as a linker, and self-assembly of this gelator molecules with ZnII ions results in a coordination polymer gel (CPG); Zn-TPY-TTF. The Zn-TPY-TTF CPG shows high photocatalytic activity towards H2 production (530 μmol g−1h−1) and CO2 reduction to CO (438 μmol g−1h−1, selectivity > 99%) regulated by charge-transfer interactions. Furthermore, in situ stabilization of Pt nanoparticles on CPG (Pt@Zn-TPY-TTF) enhances H2 evolution (14727 μmol g−1h−1). Importantly, Pt@Zn-TPY-TTF CPG produces CH4 (292 μmol g−1h−1, selectivity > 97%) as CO2 reduction product instead of CO. The real-time CO2 reduction reaction is monitored by in situ DRIFT study, and the plausible mechanism is derived computationally.



2007 ◽  
Vol 63 (a1) ◽  
pp. s150-s150
Author(s):  
N. Rahahlia ◽  
K. Aliouane ◽  
A. Guehria-Laidoudi ◽  
S. Dahaoui ◽  
C. Lecomte


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