Multiple Processing of Metal-Ion Coordination, Anion-Binding, Hydrogen-Bonding- Self-Assembly and p-p Stacking Subprograms in Silver (I) oordination Polymers

2008 ◽  
Vol 59 (3) ◽  
pp. 260-265 ◽  
Author(s):  
Pascal Blondeau ◽  
Yves-Marie Legrand ◽  
Arie Van Der Lee ◽  
Gihane Nasr ◽  
Mihail Barboiu

New crystalline coordination-polymers are obtained under conditions in which distinct metal ion coordination, hydrogen-bonding and p-p stacking subprograms are involved in independent binding events of ureidopyridyl ligands 1 and 2 by silver hexafluorophosphate or silver triflate. The geometrical information contained in the structure of the ligands 1 and 2 is fully exploited by the silver ion coordination and urea-self assembly or H-bond anion coordination templating features in an independent way. The resulted linear or angular sequences may serve to use the information stored in molecular components that could be read out by synergistic and sequential non-covalent subprograms. It results in linear or tubular supramolecular coordination polymers constructed in a bottom-up strategy.

Polyhedron ◽  
2009 ◽  
Vol 28 (5) ◽  
pp. 873-882 ◽  
Author(s):  
Safaa El-din H. Etaiw ◽  
Dina M. Abd El-Aziz ◽  
Ahmed S. Badr El-din

RSC Advances ◽  
2014 ◽  
Vol 4 (59) ◽  
pp. 30963-30967 ◽  
Author(s):  
Qipeng Li ◽  
Shaowu Du

Two novel 3D lanthanide supramolecular coordination polymers with lanthanide paddle wheel SBUs were synthesized through in situ generation of formate anions. Their structure and temperature dependent luminescent property are investigated.


2015 ◽  
Vol 44 (3) ◽  
pp. 1292-1302 ◽  
Author(s):  
Lakshmi Kanta Das ◽  
Carlos J. Gómez-García ◽  
Ashutosh Ghosh

Three new 2D coordination polymers of different networks with significant variation in magnetic properties have been synthesized by changing the central metal in the trinuclear nodes.


Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 819 ◽  
Author(s):  
Yun Xu ◽  
Qing-Hua Deng ◽  
Fang Ding ◽  
Ran An ◽  
Dong Liu ◽  
...  

Three new supramolecular coordination polymers, namely [Zn(1,3-BDC)(HL)]n (Polymer 1), [Zn3(1,3,5-BTC)2(HL)2(H2O)2]n (Polymer 2), and [Zn9(5-SO3-1,3-BDC)2(L)8(OH)4]n (Polymer 3), were synthesized under solvothermal conditions, based on 1H-pyrazolo[3,4-b]pyridin-3-amine (HL) along with 1,3-benzenedicarboxylate (1,3-BDC) and its derivatives, such as 1,3,5-benzenetricarboxylate (1,3,5-BTC) and 5-sulfo-1,3-benzenedicarboxylate (5-SO3-1,3-BDC). Polymers 1–3 were characterized by elemental analysis, IR spectroscopy, powder X-ray diffraction (PXRD), and single crystal X-ray diffraction analysis. Polymer 1 exhibited a two-dimensional (2D) 4-connected sql net. The neighboring 2D nets were further linked into a 3D supramolecular network by hydrogen-bonding interactions. Polymer 2 displayed a 3D (4, 4, 4)-connected network, which was further stabilized by R 2 2 (14) and S(9) hydrogen-bonding rings along with π–π interactions. The 2D sheet structure of Polymer 3 was constructed by novel quasi-linear nonanuclear Zn(II) units, which further extended into a 3D supramolecular structure by hydrogen-bonding interactions. The solid-state photoluminescence properties of Polymers 1–3 were also investigated.


2009 ◽  
Vol 2009 ◽  
pp. 1-10 ◽  
Author(s):  
Donato Monti ◽  
Sara Nardis ◽  
Manuela Stefanelli ◽  
Roberto Paolesse ◽  
Corrado Di Natale ◽  
...  

The construction of nanosized supramolecular hosts via self-assembly of molecular components is a fascinating field of research. Such intriguing class of architectures, beside their intrinsic intellectual stimuli, is of importance in many fields of chemistry and technology, such as material chemistry, catalysis, and sensor applications. Within this wide scenario, tailored solid films of porphyrin derivatives are structures of great potential for, among others, chemical sensor applications. The formation ofsupramoleculesrelays on noncovalent interactions (electrostatic, hydrogen bond, , or coordinative interactions) driven by the chemical information stored on the assembling molecules, such as shape and functional groups. This allows, for example, the formation of large well-defined porphyrin aggregates in solution that can be spontaneously transferred onto a solid surface, so achieving a solid system with tailored features. These films have been used, covering the bridge between nanostructures and microsystems, for the construction of solid-state sensors for volatiles and metal ion recognition and detection. Moreover, the variation of peripheral substituents of porphyrins, such as, for example, chiral appended functionalities, can result in the formation of porphyrin aggregates featuring high supramolecular chirality. This would allow the achievement of porphyrin layers characterised by different chiroptical and molecular recognition properties.


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