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      Chiral Bifunctional Thioureas and Squaramides Grafted into Old Polymers of Intrinsic Microporosity for Novel Applications

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          Abstract

          We have prepared different polymeric chiral bifunctional thioureas and squaramides by modification of the very well-known polymers of intrinsic microporosity (PIM), specifically PIM-1 and PIM-CO-1, to be used as recoverable organocatalysts. The installation of the chiral structures into the polymers has been done in two or three steps in high yields. The catalytic activity of the resulting materials has been proved in the stereoselective nitro-Michael addition and in a cascade process, which allows the synthesis of enantioenriched 4H-chromene derivatives. Squaramide II and thiourea III have been used in six cycles maintaining their activity.

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          Polymers of intrinsic microporosity (PIMs): robust, solution-processable, organic nanoporous materials.

          Microporous materials can be derived directly from soluble polymers whose randomly contorted shapes prevent an efficient packing of the macromolecules in the solid state.
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            Polymer nanosieve membranes for CO2-capture applications.

            Microporous organic polymers (MOPs) are of potential significance for gas storage, gas separation and low-dielectric applications. Among many approaches for obtaining such materials, solution-processable MOPs derived from rigid and contorted macromolecular structures are promising because of their excellent mass transport and mass exchange capability. Here we show a class of amorphous MOP, prepared by [2+3] cycloaddition modification of a polymer containing an aromatic nitrile group with an azide compound, showing super-permeable characteristics and outstanding CO(2) separation performance, even under polymer plasticization conditions such as CO(2)/light gas mixtures. This unprecedented result arises from the introduction of tetrazole groups into highly microporous polymeric frameworks, leading to more favourable CO(2) sorption with superior affinity in gas mixtures, and selective CO(2) transport by presorbed CO(2) molecules that limit access by other light gas molecules. This strategy provides a direction in the design of MOP membrane materials for economic CO(2) capture processes.
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              Exploitation of Intrinsic Microporosity in Polymer-Based Materials

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                Author and article information

                Journal
                Polymers (Basel)
                Polymers (Basel)
                polymers
                Polymers
                MDPI
                2073-4360
                21 December 2018
                January 2019
                : 11
                : 1
                : 13
                Affiliations
                Instituto CINQUIMA and Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Valladolid, Paseo de Belén 7, 47011 Valladolid, Spain; mariavallealvarez@ 123456hotmail.com (M.V.); laura.martinm@ 123456uva.es (L.M.); amaestro@ 123456qo.uva.es (A.M.)
                Author notes
                [* ]Correspondence: jmandres@ 123456qo.uva.es (J.M.A.); pedrosa@ 123456qo.uva.es (R.P.)
                Author information
                https://orcid.org/0000-0002-0595-3789
                https://orcid.org/0000-0002-3652-7301
                Article
                polymers-11-00013
                10.3390/polym11010013
                6401694
                50995ba6-8473-49a7-921a-f9ba86d3c0c3
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 23 November 2018
                : 18 December 2018
                Categories
                Article

                organocatalysis,supported catalysts,polymers of intrinsic microporosity,asymmetric nitro-michael reaction,thioureas,squaramides

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