Synthesis, molecular and supramolecular structures, electrochemistry and magnetic properties of two macrocyclic dicopper(II) complexes: Microporous supramolecular assembly

Polyhedron ◽  
2009 ◽  
Vol 28 (17) ◽  
pp. 3707-3714 ◽  
Author(s):  
Susanta Hazra ◽  
Samit Majumder ◽  
Michel Fleck ◽  
Núria Aliaga-Alcalde ◽  
Sasankasekhar Mohanta
2016 ◽  
Vol 16 (10) ◽  
pp. 5624-5635 ◽  
Author(s):  
Cheng-Qi Jiao ◽  
Zhou Zhao ◽  
Chao Ma ◽  
Zhen-Gang Sun ◽  
Da-Peng Dong ◽  
...  

2015 ◽  
Vol 11 ◽  
pp. 1596-1613 ◽  
Author(s):  
Masahiko Iyoda ◽  
Masashi Hasegawa

The construction of redox-active supramolecular assemblies based on star-shaped and radially expanded tetrathiafulvalene (TTF) oligomers with divergent and extended conjugation is summarized. Star-shaped TTF oligomers easily self-aggregate with a nanophase separation to produce supramolecular structures, and their TTF units stack face-to-face to form columnar structures using the fastener effect. Based on redox-active self-organizing supramolecular structures, conducting nanoobjects are constructed by doping of TTF oligomers with oxidants after the formation of such nanostructures. Although radical cations derived from TTF oligomers strongly interact in solution to produce a mixed-valence dimer and π-dimer, it seems to be difficult to produce nanoobjects of radical cations different from those of neutral TTF oligomers. In some cases, however, radical cations form nanostructured fibers and rods by controlling the supramolecular assembly, oxidation states, and counter anions employed.


2006 ◽  
Vol 45 (9) ◽  
pp. 3639-3647 ◽  
Author(s):  
M. Carmen Barral ◽  
Teresa Gallo ◽  
Santiago Herrero ◽  
Reyes Jiménez-Aparicio ◽  
M. Rosario Torres ◽  
...  

2014 ◽  
Vol 20 (36) ◽  
pp. 11362-11369 ◽  
Author(s):  
Tomoko Inose ◽  
Daisuke Tanaka ◽  
Hirofumi Tanaka ◽  
Oleksandr Ivasenko ◽  
Toshi Nagata ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (93) ◽  
pp. 90754-90759 ◽  
Author(s):  
Alessandro Ruffoni ◽  
Maria V. Cavanna ◽  
Simona Argentiere ◽  
Silvia Locarno ◽  
Sara Pellegrino ◽  
...  

The preparation and self-assembly of short hydrophobic peptides containing the non-coded norbornene amino acid is reported. The formation of a supramolecular assembly in water was assessed by TEM and DLS.


2000 ◽  
Vol 78 (6) ◽  
pp. 723-731 ◽  
Author(s):  
Stefano Roelens ◽  
Paolo Dapporto ◽  
Paola Paoli

A new H-bonded supramolecular assembly of the diamine-diol family has been obtained from (1R,2R)-1,2-diaminocyclohexane (DAC) and (S)-1-phenyl-1,2-ethanediol (PED). The structure was characterized by single-crystal X-ray analysis and showed the typical architecture of DAC based assemblies, consisting of a three-stranded helicate coiling around a H-bonded core, with a predictable helicity sense determined by the configuration of DAC. The new assembly, while reconfirming the unique role of DAC as a powerful assembler of supramolecular structures, demonstrated that the C2 symmetry of diol partners employed so far is not essential for assembling helicates, although chirality is. In the case of the adduct between (1R,2R)-1,2-diaminocyclohexane and (2R,3R)-2,3-butanediol, molecular recognition and self-assembly have been shown to take place even in the absence of solvent, in the gas phase, where long crystals were formed by spontaneous organized aggregation of diamine-diol units. A thorough analysis of the results from the present and previous investigations has lead to a deeper understanding of the key features of the diamine-diol molecular code and of the requirements for recognition and assembly.Key words: supramolecular, hydrogen bonding, molecular recognition, self-assembly, diamines, diols.


2014 ◽  
Vol 20 (36) ◽  
pp. 11237-11237 ◽  
Author(s):  
Tomoko Inose ◽  
Daisuke Tanaka ◽  
Hirofumi Tanaka ◽  
Oleksandr Ivasenko ◽  
Toshi Nagata ◽  
...  

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