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      Bis(benzylamine) monomers: One-pot preparation and application in dendrimer scaffolds for removing pyrene from aqueous environments

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          Summary

          Bisimine and bisamine AB 2 monomers have been synthesized from 3,5-diaminobenzoic acid and benzaldehyde derivatives without the need for protective groups or purification. This monomer preparation is universal for various electron-donating and electron-withdrawing benzaldehyde substrates. To demonstrate the versatility of these previously unreported AB 2 monomers in the formation of high molecular weight structures, novel first-generation dendrimers and hybrid second-generation dendrimers have been synthesized. Using fluorescence spectroscopy, pyrene was shown to be removed from an aqueous environment upon exposure to thin dendrimer films, with the first-generation dendrimer removing 70% of the pyrene within 30 min and the hybrid second-generation dendrimers removing 38–52%. Inclusion formation constants were calculated to be on the order of 10 9–10 11 M −1 and are comparable to the values of previously reported macromolecules. These results illustrate that size may not influence pyrene removal as effectively as composition.

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          Most cited references31

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          Applications of orthogonal "click" chemistries in the synthesis of functional soft materials.

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            Convergent dendrons and dendrimers: from synthesis to applications.

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              Green chemistry for chemical synthesis.

              Green chemistry for chemical synthesis addresses our future challenges in working with chemical processes and products by inventing novel reactions that can maximize the desired products and minimize by-products, designing new synthetic schemes and apparati that can simplify operations in chemical productions, and seeking greener solvents that are inherently environmentally and ecologically benign.
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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Beilstein J Org Chem
                Beilstein J Org Chem
                Beilstein Journal of Organic Chemistry
                Beilstein-Institut (Trakehner Str. 7-9, 60487 Frankfurt am Main, Germany )
                1860-5397
                2013
                31 October 2013
                : 9
                : 2320-2327
                Affiliations
                [1 ]Department of Chemistry, Fordham University, 441 E. Fordham Road, Bronx, NY 10458, USA
                Article
                10.3762/bjoc.9.266
                3869215
                24367395
                7b9bdbd2-7bf3-42f7-8b72-f006f134b665
                Copyright © 2013, Monaco et al; licensee Beilstein-Institut.

                This is an Open Access article under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: ( http://www.beilstein-journals.org/bjoc)

                History
                : 1 July 2013
                : 7 October 2013
                Categories
                Full Research Paper
                Chemistry
                Organic Chemistry

                Organic & Biomolecular chemistry
                amines,dendrimer,fluorescence studies,imines,pyrene
                Organic & Biomolecular chemistry
                amines, dendrimer, fluorescence studies, imines, pyrene

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