Interparticle Charge Transfer Mediated by π−π Stacking of Aromatic Moieties

2007 ◽  
Vol 129 (35) ◽  
pp. 10622-10623 ◽  
Author(s):  
Sulolit Pradhan ◽  
Debraj Ghosh ◽  
Li-Ping Xu ◽  
Shaowei Chen
Keyword(s):  
Author(s):  
Wenjuan Xu ◽  
Yupei Sun ◽  
Xiangru Meng ◽  
Wenjing Zhang ◽  
Hongwei Hou

Three π–π stacked CPs were designed and synthesized for application of photoelectric response. The effect of charge transfer on the photoelectric properties is explored by adjusting the composition and π-stacking fashion of the CPs.


2018 ◽  
Vol 42 (13) ◽  
pp. 10615-10622 ◽  
Author(s):  
Chideraa I. Nwachukwu ◽  
Zachary R. Kehoe ◽  
Nathan P. Bowling ◽  
Erin D. Speetzen ◽  
Eric Bosch

Matched electron rich halogen bond acceptors and donor have been synthesized and the halogen bonded charge transfer cocrystals characterized.


2014 ◽  
Vol 67 (6) ◽  
pp. 887 ◽  
Author(s):  
Ting-Hong Huang ◽  
Min-Hua Zhang

Based on the ligands N,N′-bis(pyridin-2-ylmethylene)benzene-1,4-diamine (pmb) and N,N′-bis(pyridin-2-ylmethylene)biphenyl-4,4′-diamine (pmbb), the three compounds [Cu2(pmb) (PPh3)2(Cl)2] (1), [Cu2(pmbb)(CH3CN)2(PPh3)2](BF4)2·2DMF (2), and [Ag2(pmbb)(PPh3)2] (ClO4)2 (3) have been synthesised and characterised. Structural analysis reveals that all of these complexes contain 1D supramolecular arrays, with different variations in π-stacking patterns and intermolecular C–H···π interactions. Crystal structures of 1 and 2 contain 1D tape-like arrays formed by C–H···π and π···π interactions, and an ordered-layer-lattice of DMF and BF4– in 2 is located between the one-dimensional array. For 3, π-stacking interactions lead to the construction of 1D supramolecular arrays and a 2D network. The results indicate that C–H···π and π···π interactions play an important role in the construction of the supramolecular structure. In addition, the absorption peaks of complexes 1 and 3 in the solid state at room temperature show intraligand charge transfer and metal-to-ligand charge transfer absorptions. The optical and fluorescent properties of 2 were also studied in acetonitrile solution at room temperature.


Author(s):  
ALI NAVID ◽  
EDUARD M. TYAPOCHKIN ◽  
CHARLES J. ARCHER ◽  
EVGUENII I. KOZLIAK

Intermediates of the cobalt tetrasulfophthalocyanine ( CoTSPc )-catalyzed thiol autoxidation were studied by UV-vis spectroscopy. All thiolates react with CoTSPc resulting in the formation of 1:1 complexes. Three major factors control both the stability and aggregation of the complexes: thiolate basicity, metal-to-ligand charge transfer (MLCT) and π stacking. Basic thiolates partially reduce C oII TSPc , whereas CoTSPc complexes with low-basicity aliphatic thiolates ( p K a < 4) do not exhibit Co (II) reduction, based on the absence of the characteristic Co (I) charge transfer band at 450 nm. CoTSPc complexes with aliphatic and bulky aromatic thiolates appear to be aggregated in aqueous solutions and are characterized by a broad band at 650 nm. Non-bulky aromatic thiolates of low basicity ( p K a < 6) form unique stable monomeric Co II TSPc complexes. This unique spectral feature can be attributed to π stacking between the phthalocyanine ring and thiolate. Comparison of binding constants shows that the partial reduction of Co (II) significantly contributes to the thiolate binding. A combination of aromatic π stacking and MLCT appears to be responsible for the observed 1000-fold stronger binding of non-basic aromatic thiolates as compared with aliphatic ligands of similar basicity. Kinetic studies confirm the importance of the thiolate binding type for catalysis.


1997 ◽  
Vol 52 (4) ◽  
pp. 485-489 ◽  
Author(s):  
Teodor Silviu Balaban ◽  
Nina G. Furmanova

Abstract The crystal structures of two isomeric phenyl-substituted pyrylium perchlorates, 2,6-di-methyl-4-phenylpyrylium (1) and 2,4-dim ethyl-6-phenylpyrylium (2), have been determined. Both cations are planar in the crystal so that the electron deficient pyrylium rings can interact strongly with the phenyl rings of adjacent molecules forming stacks along the shortest crystallographic axis. The phenyl rings may act as donors in a charge transfer interaction which is more pronounced in 1 than in 2. Charge transfer appears as a non-mandatory consequence of the π-π stacking. The structures demonstrate the electrostatic nature of these interactions conforming to the model of Hunter and Sanders [ 1 ].


Author(s):  
Nathan Yee ◽  
Afshin Dadvand ◽  
Ehsan Hamzehpoor ◽  
Hatem M. Titi ◽  
Dmitrii F. Perepichka

Langmuir ◽  
2010 ◽  
Vol 26 (9) ◽  
pp. 6630-6637 ◽  
Author(s):  
Antti Tolkki ◽  
Elina Vuorimaa ◽  
Vladimir Chukharev ◽  
Helge Lemmetyinen ◽  
Petri Ihalainen ◽  
...  

2020 ◽  
Vol 7 (6) ◽  
pp. 1451-1466 ◽  
Author(s):  
Wei Wu ◽  
Xiang-Ling Lin ◽  
Qian Liu ◽  
Yan He ◽  
You-Ren Huang ◽  
...  

Good electrical bistability performances in stilbazolium/iodocuprate hybrids stem from the better face-to-face π⋯π stacking interactions induced by the substituents with appropriate lengths and electronic natures.


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