Ultrafast Internal Dynamics of Flexible Hydrogen-Bonded Supramolecular Complexes

2011 ◽  
Vol 115 (7) ◽  
pp. 1210-1221 ◽  
Author(s):  
Martin Olschewski ◽  
Stephan Knop ◽  
Jaane Seehusen ◽  
Jörg Lindner ◽  
Peter Vöhringer
RSC Advances ◽  
2014 ◽  
Vol 4 (81) ◽  
pp. 42983-42990 ◽  
Author(s):  
Hengjun Chen ◽  
Min Li ◽  
Guiming Zheng ◽  
Yifang Wang ◽  
Yang Song ◽  
...  

Structures of three D–A supramolecular systems and their photoresponsive characteristics are investigated.


Author(s):  
Marina V. Fomina ◽  
Alexander S. Nikiforov ◽  
Vitaly G. Avakyan ◽  
Artem I. Vedernikov ◽  
Nikolai A. Kurchavov ◽  
...  

2015 ◽  
Vol 3 (44) ◽  
pp. 11735-11746 ◽  
Author(s):  
Ke-Qing Zhao ◽  
Xiao-Yan Bai ◽  
Bo Xiao ◽  
Yue Gao ◽  
Ping Hu ◽  
...  

The synthesis and self-assembly properties of four novel star-shaped oligomers containing triphenylene discotic mesogens are reported.


2015 ◽  
Vol 143 (10) ◽  
pp. 104309 ◽  
Author(s):  
Rebecca B. Mackenzie ◽  
Christopher T. Dewberry ◽  
Emma Coulston ◽  
George C. Cole ◽  
Anthony C. Legon ◽  
...  

2014 ◽  
Vol 926-930 ◽  
pp. 68-71
Author(s):  
Zhi Lian Liu ◽  
Xiao Hui Li ◽  
Zhen Ning Yu

A new series of supramolecular hydrogen-bonded liquid cryatals complexes were synthesized based on pyridine derivative and 4-n-alkoxybenzoic acids. The formation of hydrogen bonds was verified by infrared spectra. The thermal behavior of supramolecular liquid crystals was studied using differential scanning calorimeter (DSC). The liquid crystal texture was revealed with polarizing optical microscope (POM). It demonstrats that all supramolecular complexes have good liquid crystal properties.


Crystals ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 133 ◽  
Author(s):  
Hoda Ahmed ◽  
Mohamed Hagar ◽  
Omaima Alhaddad

Four new series of laterally methyl-substituted hydrogen-bonded supramolecular complexes were prepared. The prepared complexes were thermally investigated by differential scanning calorimetry (DSC) and phases identified by polarized light microscopy (PLM). Supramolecular hydrogen-bonded complexes formed from a 1:1 mixture of any two derivatives, bearing different alkoxy chains, of 4-alkoxyphenylazobenzoic acid and 4-(2-(pyridin-4-yl)diazenyl-(2-(or 3-)methylphenyl) 4-alkoxybenzoate. The investigated 1:1 mixture made by introducing a lateral methyl group by different spatial orientation angles into pyridine-based components. All new complexes were confirmed by Fourier-transform infrared spectroscopy (FTIR) and computational calculations used to study their stabilities. It is found that the prepared complexes are dimorphic, exhibiting smectic C and enhanced nematic phases. A comparison was made between the new series and previously investigated simpler complexes, revealed that the incorporation of the phenylazo group elongate the mesogenic part and hence broad nematic phases were obtained with high stability.


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