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      Nanoscale metallogel via self-assembly of self-assembled trinuclear coordination rings: multi-stimuli-responsive soft materials

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      Dalton Transactions
      Royal Society of Chemistry (RSC)

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          Abstract

          A multi-stimuli-responsive metallogel is obtained by the self-assembly of an already self-assembled trinuclear palladium( ii) based coordination ring of the rare M 3L 6 composition.

          Abstract

          A rare variety of coordination rings having the M 3L 6 composition are prepared by the combination of Pd(NO 3) 2 with an imidazolyl or benzimidazolyl appended bidentate non-chelating ligand ( i.e. L1 or L2). The variable concentration 1H NMR spectra of the trinuclear complexes [Pd 3( L1) 6](NO 3) 6, 1a and [Pd 3( L2) 6](NO 3) 6, 2a in DMSO-d 6 provided valuable information on the self-assembly phenomenon of the already self-assembled complexes. Interestingly, the signals of 2a are broadened upon increasing the concentration. The solution of 2a in DMSO formed a supramolecular metallogel above a certain concentration ( i.e. 2% w/v), however, complex 1a could not form any gel. This phenomenon is attributed to the presence of an auxiliary π-surface in the benzimidazole moiety in L2, in contrast to the imidazole moiety of L1. The influence of anions in gel formation was studied by preparing several samples using a variety of palladium( ii) salts and L2 in DMSO. It was found that oxoanions like nitrate, perchlorate, triflate and tosylate are amicable for gel formation, probably due to their capabilities of forming H-bonds. The counter anions like tetrafluoroborate, hexafluorophosphate, or hexafluoroantimonate could not assist in the formation of gel. The stimuli-responsive nature of the gel and the reversible gel–sol conversion were demonstrated by dis-assembly and re-assembly processes of 2a as controlled by a pair of stimuli such as halide-nitrate, DMAP-HNO 3, and ethylenediamine-Pd(NO 3) 2. No gel could be prepared by the combination of Ni(NO 3) 2 or Pt(NO 3) 2 with ligand L2. Thus, a subtle change in the ligand design, metal ion and counter anion is demonstrated as the responsible parameter for the construction of the three component multi-stimuli-responsive supramolecular gel.

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          Functional Molecular Flasks: New Properties and Reactions within Discrete, Self-Assembled Hosts

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            Stimuli-responsive supramolecular polymeric materials.

            Supramolecular materials, dynamic materials by nature, are defined as materials whose components are bridged via reversible connections and undergo spontaneous and continuous assembly/disassembly processes under specific conditions. On account of the dynamic and reversible nature of noncovalent interactions, supramolecular polymers have the ability to adapt to their environment and possess a wide range of intriguing properties, such as degradability, shape-memory, and self-healing, making them unique candidates for supramolecular materials. In this critical review, we address recent developments in supramolecular polymeric materials, which can respond to appropriate external stimuli at the fundamental level due to the existence of noncovalent interactions of the building blocks.
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              Coordination assemblies from a Pd(II)-cornered square complex.

              The [enPd(II)]2+ (en = ethylenediamine) unit has emerged as a versatile building block in molecular self-assembly. In particular, the 90 degrees coordination angle of the metal has been judiciously used in the design of new discrete two- and three-dimensional structures. Our last 15 years of work with the Pd(II)-cornered unit is summarized in this Account, from the spontaneous formation of a Pd4 square metal complex to a family of architectures such as cages, bowls, boxes, tubes, catenanes, and spheres.
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                Author and article information

                Journal
                ICHBD9
                Dalton Transactions
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                2015
                2015
                : 44
                : 34
                : 15181-15188
                Article
                10.1039/C4DT03715D
                25826610
                8f62e578-ba4b-4ed6-ace9-bb2dad8086ee
                © 2015
                History

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