Mercury supramolecular architectures constructed from flexible unsymmetrical bis(pyridyl) ligands: Structural motif mediated by mercury-halide clusters, ligand conformations and non-covalent interactions

Polyhedron ◽  
2016 ◽  
Vol 117 ◽  
pp. 338-351 ◽  
Author(s):  
Zheng-Yang Ye ◽  
Zhu-Yan Zhang ◽  
Li-Hua Huo ◽  
Zhao-Peng Deng ◽  
Xian-Fa Zhang ◽  
...  
2021 ◽  
Vol 45 (4) ◽  
pp. 2249-2263
Author(s):  
Pretam Kumar ◽  
Snehasis Banerjee ◽  
Anu Radha ◽  
Tahira Firdoos ◽  
Subash Chandra Sahoo ◽  
...  

The H-bond, spodium bond and CH⋯π interactions playing an important role in the supramolecular organization of two mercury(ii) diphenyldithiophosphate complexes have been discussed.


2015 ◽  
Vol 39 (4) ◽  
pp. 2778-2794 ◽  
Author(s):  
Debanjana Biswal ◽  
Nikhil Ranjan Pramanik ◽  
Syamal Chakrabarti ◽  
Nirmalya Chakraborty ◽  
Krishnendu Acharya ◽  
...  

Fascinating supramolecular frameworks of Mo(vi) complexes.


2020 ◽  
Vol 21 (24) ◽  
pp. 9458
Author(s):  
Sayuri L. Higashi ◽  
Normazida Rozi ◽  
Sharina Abu Hanifah ◽  
Masato Ikeda

Supramolecular architectures that are built artificially from biomolecules, such as nucleic acids or peptides, with structural hierarchical orders ranging from the molecular to nano-scales have attracted increased attention in molecular science research fields. The engineering of nanostructures with such biomolecule-based supramolecular architectures could offer an opportunity for the development of biocompatible supramolecular (nano)materials. In this review, we highlighted a variety of supramolecular architectures that were assembled from both nucleic acids and peptides through the non-covalent interactions between them or the covalently conjugated molecular hybrids between them.


2019 ◽  
Vol 20 (20) ◽  
pp. 5004 ◽  
Author(s):  
Agnieszka Czapik ◽  
Maciej Jelecki ◽  
Marcin Kwit

The molecular recognition process and the ability to form multicomponent supramolecular systems have been investigated for the amide of triphenylacetic acid and l-tyrosine (N-triphenylacetyl-l-tyrosine, TrCOTyr). The presence of several supramolecular synthons within the same amide molecule allows the formation of various multicomponent crystals, where TrCOTyr serves as a chiral host. Isostructural crystals of solvates with methanol and ethanol and a series of binary crystalline molecular complexes with selected organic diamines (1,5-naphthyridine, quinoxaline, 4,4′-bipyridyl, and DABCO) were obtained. The structures of the crystals were planned based on non-covalent interactions (O–H···N or N–H+···O− hydrogen bonds) present in a basic structural motif, which is a heterotrimeric building block consisting of two molecules of the host and one molecule of the guest. The complex of TrCOTyr with DABCO is an exception. The anionic dimers built off the TrCOTyr molecules form a supramolecular gutter, with trityl groups located on the edge and filled by DABCO cationic dimers. Whereas most of the racemic mixtures crystallize as racemic crystals or as conglomerates, the additional tests carried out for racemic N-triphenylacetyl-tyrosine (rac-TrCOTyr) showed that the compound crystallizes as a solid solution of enantiomers.


Polyhedron ◽  
2015 ◽  
Vol 89 ◽  
pp. 304-312 ◽  
Author(s):  
Vinod Kumar ◽  
Vikram Singh ◽  
Ajit N. Gupta ◽  
Santosh Kumar Singh ◽  
Michael G.B. Drew ◽  
...  

2001 ◽  
Vol 635 ◽  
Author(s):  
Andrew K. Boal ◽  
Vincent M. Rotello

AbstractUnlike the highly ordered Self-Assembled Monolayers (SAMs) formed on flat gold surfaces, those on gold nanoparticles radiate from a roughly spherical center and are amorphous in structure. One result of this structural motif is that the strength of intra- monolayer non-covalent interactions, such as Φ-stacking and hydrogen bonding, are a function of the distance of the recognition element from the colloidal core. We present here an exploration of these phenomena in amide functionalized thiols in MPCs where the amide functionality position was varied in the alkane chain. [1]


Sign in / Sign up

Export Citation Format

Share Document