Trinuclear Complexes and Coordination Polymers of Redox-Active Guanidino-Functionalized Aromatic (GFA) Compounds with a Triphenylene Core

2014 ◽  
Vol 53 (18) ◽  
pp. 9876-9896 ◽  
Author(s):  
Anna Lebkücher ◽  
Christoph Wagner ◽  
Olaf Hübner ◽  
Elisabeth Kaifer ◽  
Hans-Jörg Himmel
2021 ◽  
Author(s):  
Omar Salinas ◽  
Jiaze Xie ◽  
Robert Papoular ◽  
Noah Horwitz ◽  
Erik Elkaim ◽  
...  

One of the notable advantages of molecular materials is the ability to precisely tune structure, properties, and function via molecular substitutions. While many studies have demonstrated this principle with classic...


Author(s):  
Zhi-Qing Lin ◽  
Sai-Li Zheng ◽  
Jie-Ying Hu ◽  
Hua-Qun Zhou ◽  
Zihao Feng ◽  
...  

Cu(I)-based cyclic trinuclear complexes (CTCs) represent one of the most intensively investigated candidates in coinage metal-derived CTCs because of their rich photoluminescent properties. Beyond molecular level, coordination polymers built upon...


2020 ◽  
Vol 26 (49) ◽  
pp. 11063-11063
Author(s):  
Marcus W. Drover ◽  
Maeve C. Dufour ◽  
Lindsay A. Lesperance‐Nantau ◽  
Rayni P. Noriega ◽  
Kirill Levin ◽  
...  

2009 ◽  
Vol 62 (10) ◽  
pp. 1214 ◽  
Author(s):  
Sharizal Hasan ◽  
Nathan L. Kilah ◽  
Manuel Martinez ◽  
Paul V. Bernhardt

The new cyanido-bridged mixed valent FeII/CoIII macrocyclic complexes [L2CoIII(μ-NC)FeII(CN)5]– and trans-[L2CoIII(μ-NC)FeII(CN)4(μ-CN)CoIIIL2]2+ have been prepared and characterized spectroscopically. The trinuclear complex trans-[L2Co(μ-NC)Fe(CN)4(μ-CN)CoL2](ClO4)2·11H2O has been characterized crystallographically. The di- and trinuclear complexes exhibit metal-to-metal charge transfer transitions characteristic of Class II mixed valent chromophores and their redox and spectroscopic properties have been analyzed by Hush theory. The thiophene group attached to the macrocycle L2 in these complexes may serve as a precursor to conducting polythiophene-based hybrid materials incorporating redox active transition metal ions.


2021 ◽  
Author(s):  
Omar Salinas ◽  
Jiaze Xie ◽  
Robert J. Papoular ◽  
Noah E. Horwitz ◽  
Erik Elkaim ◽  
...  

<div>One of the notable advantages of molecular materials is the ability to precisely tune structure, properties, and function via molecular substitutions. While many studies have demonstrated this principle with classic carboxylate‐based coordination polymers, there are comparatively fewer examples where systematic changes to sulfur‐based coordination polymers have been investigated. Here we present such a study on 1D coordination chains of redox‐active</div><div>iron-sulfur clusters linked by methylated 1,4‐benzene‐dithiolates. A series of new iron-sulfur based coordination polymers were synthesized with either 2,5‐dimethyl‐1,4‐benzenedithiol (DMBDT) or 2,3,5,6‐tetramethyl‐1,4‐benzenedithiol. The structures of these compounds have been characterized based on synchrotron Xray</div><div>powder diffraction while their chemical and physical properties have been characterized by techniques including X‐ray photoelectron spectroscopy, cyclic voltammetry and UV–visible spectroscopy. Methylation results in the general trend of increasing electron‐richness in the series, but the tetramethyl version exhibits unexpected properties arising from steric constraints. All these results highlight how substitutions on organic linkers can modulate electronic factors to fine‐tune the electronic structures of metal‐organic materials.</div>


2021 ◽  
Vol 1231 ◽  
pp. 129948
Author(s):  
Wen-Jing Xu ◽  
Kun-Peng Chen ◽  
Yue Zhang ◽  
Yue Ma ◽  
Quan-Wen Li ◽  
...  

2021 ◽  
Author(s):  
Yong Yan ◽  
Stefan Henfling ◽  
Ning ning Zhang ◽  
Harald Krautscheid

Two semiconductive coordination polymers based on a chelating redox-active ligand were synthesized and structurally characterized. Strong and continuous intermolecular π-π interactions are likely the reason for moderate electrical conductivity of...


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