1,2,3-Triazole-Functionalized Polysulfone Synthesis through Microwave-Assisted Copper-Catalyzed Click Chemistry: A Highly Proton Conducting High Temperature Membrane.

Microwave heating holds all the aces regarding development of effective and environmentally friendly methods to perform chemical transformations. Coupling the benefits of microwave-enhanced chemistry with highly reliable copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry paves the way for a rapid and efficient synthesis procedure to afford high performance thermoplastic materials. We describe herein fast and high yielding synthesis of 1,2,3-triazole-functionalized polysulfone through microwave-assisted CuAAC as well as explore their potential as phosphoric acid doped polymer electrolyte membranes (PEM) for high temperature PEM fuel cells. Polymers with various degrees of substitution of the side-chain functionality of 1,4-substituted 1,2,3-triazole with alkyl and aryl pendant structures are prepared by sequential chloromethylation, azidation, and microwave-assisted CuAAC using a range of alkynes (1-pentyne, 1-nonyne, and phenylacetylene). The completeness of reaction at each step and the purity of the clicked polymers were confirmed by (1)H-(13)C NMR, DOSY-NMR and FTIR-ATR spectroscopies. The thermal and thermochemical properties of the modified polymers were characterized by differential scanning calorimetry and thermogravimetric analysis coupled with mass spectroscopy (TG-MS), respectively. TG-MS analysis demonstrated that the commencement of the thermal degradation takes place with the decomposition of the triazole ring while its substituents have critical influence on the initiation temperature. Polysulfone functionalized with 4-phenyl-1,2,3-triazole demonstrates significantly higher Tg, Td, and elastic modulus than the ones bearing 4-propyl-1,2,3-triazole and 4-heptyl-1,2,3-triazole groups. After doping with phosphoric acid, the functionalized polymers with acid doping level of 5 show promising performance with high proton conductivity in anhydrous conditions (in the range of 27-35 mS/cm) and satisfactorily high elastic modulus (in the range of 332-349 MPa).

[1]  M. Heravi,et al.  Computational Studies on the Regioselectivity of Metal‐Catalyzed Synthesis of 1,2,3 Triazoles via Click Reaction: A Review , 2016 .

[2]  Deborah J. Jones,et al.  New semi-IPN PEMFC membranes composed of crosslinked fluorinated copolymer bearing triazole groups and sPEEK for operation at low relative humidity , 2015 .

[3]  F. Alonso,et al.  Copper Nanoparticles in Click Chemistry , 2015 .

[4]  A. Burke,et al.  New Click‐Chemistry Methods for 1,2,3‐Triazoles Synthesis: Recent Advances and Applications , 2015 .

[5]  M. Heravi,et al.  In situ prepared copper nanoparticles on modified KIT-5 as an efficient recyclable catalyst and its applications in click reactions in water , 2015 .

[6]  M. Heravi,et al.  Magnetic nano-Fe3O4@TiO2/Cu2O core–shell composite: an efficient novel catalyst for the regioselective synthesis of 1,2,3-triazoles using a click reaction , 2015 .

[7]  Biao Zhang,et al.  Triethylene glycol-based poly(1,2,3-triazolium acrylate)s with enhanced ionic conductivity , 2015 .

[8]  M. Heravi,et al.  Recent Applications of Click Reaction in the Syntheses of 1,2,3-Triazoles , 2014 .

[9]  Mukesh C. Sharma,et al.  A click chemistry strategy to synthesize geraniol-coupled 1,4-disubstituted 1,2,3-triazoles and exploration of their microbicidal and antioxidant potential with molecular docking profile , 2015, Medicinal Chemistry Research.

[10]  W. Dehaen Chemistry of 1,2,3-triazoles , 2015 .

[11]  Biao Zhang,et al.  1,2,3-Triazolium-based poly(acrylate ionic liquid)s , 2014 .

[12]  Deborah J. Jones,et al.  Anhydrous proton motion study by solid state NMR spectroscopy in novel PEMFC blend membranes composed of fluorinated copolymer bearing 1,2,4-triazole functional groups and sPEEK , 2014 .

[13]  M. Heravi,et al.  In situ prepared CuI nanoparticles on modified poly(styrene-co-maleic anhydride): an efficient and recyclable catalyst for the azide–alkyne click reaction in water , 2014, Transition Metal Chemistry.

[14]  Rajender S. Varma,et al.  Microwave-assisted chemistry: synthetic applications for rapid assembly of nanomaterials and organics. , 2014, Accounts of chemical research.

[15]  A. Serghei,et al.  1,2,3-Triazolium-Based Poly(ionic liquid)s with Enhanced Ion Conducting Properties Obtained through a Click Chemistry Polyaddition Strategy , 2014 .

[16]  W. Dehaen,et al.  Thermal Rearrangements and Transformations of 1,2,3-Triazoles , 2014 .

[17]  M. Heravi,et al.  Green and Facile Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via a Click Reaction of α-Bromo Ketones, [bmim]N 3 and Terminal Acetylenes , 2013 .

[18]  M. Guiver,et al.  Towards high conductivity in anion-exchange membranes for alkaline fuel cells. , 2013, ChemSusChem.

[19]  Deborah J. Jones,et al.  Novel Blend Membranes of Partially Fluorinated Copolymers Bearing Azole Functions with Sulfonated PEEK for PEMFC Operating at Low Relative Humidity: Influence of the Nature of the N-Heterocycle , 2013 .

[20]  R. Benhida,et al.  Microwave‐Assisted Cycloaddition Reactions , 2013 .

[21]  Patric Jannasch,et al.  Polysulfone functionalized with phosphonated poly(pentafluorostyrene) grafts for potential fuel cell applications. , 2012, Macromolecular rapid communications.

[22]  F. D. Prez,et al.  Heterogeneous azide–alkyne click chemistry: towards metal-free end products , 2012 .

[23]  Matthew D. Green,et al.  Alkyl‐Substituted N‐Vinylimidazolium Polymerized Ionic Liquids: Thermal Properties and Ionic Conductivities , 2011 .

[24]  D. Ionita,et al.  Chemical modification of chloromethylated polysulfones via click reactions , 2011 .

[25]  D. Wan,et al.  Preparation and Characterisation of Proton Exchange Membranes Based on Crosslinked Polybenzimidazole and Phosphoric Acid , 2010 .

[26]  A. Manthiram,et al.  Acid-base blend membranes consisting of sulfonated poly(ether ether ketone) and 5-amino-benzotriazole tethered polysulfone for DMFC , 2010 .

[27]  Nedal Y. Abu-Thabit,et al.  New highly phosphonated polysulfone membranes for PEM fuel cells , 2010 .

[28]  M. Tuominen,et al.  Hybrid inorganic–organic proton exchange membranes containing 1H-1,2,3-triazole moieties , 2010 .

[29]  Jason E Hein,et al.  Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides. , 2010, Chemical Society reviews.

[30]  C. Kappe,et al.  Click chemistry under non-classical reaction conditions. , 2010, Chemical Society reviews.

[31]  Deborah J. Jones,et al.  Synthesis and properties of new fluorinated polymers bearing pendant imidazole groups for fuel cell membranes operating over a broad relative humidity range , 2010 .

[32]  B. Tang,et al.  Click polymerization. , 2010, Chemical Society reviews.

[33]  Daniel J. Burke,et al.  Applications of orthogonal "click" chemistries in the synthesis of functional soft materials. , 2009, Chemical reviews.

[34]  F. D. Prez,et al.  Step-growth polymerization and 'click' chemistry: The oldest polymers rejuvenated , 2009 .

[35]  R. Graf,et al.  1H solid-state NMR investigation of structure and dynamics of anhydrous proton conducting triazole-functionalized siloxane polymers. , 2009, The journal of physical chemistry. B.

[36]  C. Hawker,et al.  Synthesis and Characterization of Isomeric Vinyl-1,2,3-triazole Materials by Azide−Alkyne Click Chemistry , 2009 .

[37]  A. Sokolov,et al.  Role of Chemical Structure in Fragility of Polymers: A Qualitative Picture , 2008 .

[38]  Morten Meldal,et al.  Cu-catalyzed azide-alkyne cycloaddition. , 2008, Chemical reviews.

[39]  Jeremiah A. Johnson,et al.  Construction of Linear Polymers, Dendrimers, Networks, and Other Polymeric Architectures by Copper‐Catalyzed Azide‐Alkyne Cycloaddition “Click” Chemistry , 2008 .

[40]  C. Kappe,et al.  Microwave dielectric heating in synthetic organic chemistry , 2008 .

[41]  G. Schmidt-naake,et al.  Proton Conducting Membranes Obtained by Doping Radiation-Grafted Basic Membrane Matrices with Phosphoric Acid , 2007 .

[42]  U. Schubert,et al.  Clicking polymers: a straightforward approach to novel macromolecular architectures. , 2007, Chemical Society reviews.

[43]  Jean-François Lutz,et al.  1,3-dipolar cycloadditions of azides and alkynes: a universal ligation tool in polymer and materials science. , 2007, Angewandte Chemie.

[44]  T. Zawodzinski,et al.  4,5-dicyano-1H-[1,2,3]-triazole as a proton transport facilitator for polymer electrolyte membrane fuel cells. , 2007, Journal of the American Chemical Society.

[45]  C. Hawker,et al.  A versatile new monomer family: functionalized 4-vinyl-1,2,3-triazoles via click chemistry. , 2006, Journal of the American Chemical Society.

[46]  G. McKenna,et al.  Correlation between dynamic fragility and glass transition temperature for different classes of glass forming liquids , 2006 .

[47]  G. Wegner,et al.  Anhydrous Polymeric Proton Conductors Based on Imidazole Functionalized Polysiloxane , 2006 .

[48]  G. Molnár,et al.  Thermal degradation of chemically modified polysulfones , 2005 .

[49]  Meilin Liu,et al.  Promotion of proton conduction in polymer electrolyte membranes by 1H-1,2,3-triazole. , 2005, Journal of the American Chemical Society.

[50]  H. Hiemstra,et al.  CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective , 2005 .

[51]  C. Kappe,et al.  Controlled microwave heating in modern organic synthesis. , 2004, Angewandte Chemie.

[52]  K. Cheuk,et al.  Helical Conjugated Polymers: Synthesis, Stability, and Chiroptical Properties of Poly(alkyl phenylpropiolate)s Bearing Stereogenic Pendants , 2004 .

[53]  K. Kreuer,et al.  Toward a new type of anhydrous organic proton conductor based on immobilized imidazole , 2004 .

[54]  Paul M. Hergenrother,et al.  The Use, Design, Synthesis, and Properties of High Performance/High Temperature Polymers: An Overview , 2003 .

[55]  Luke G Green,et al.  A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.

[56]  Morten Meldal,et al.  Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. , 2002, The Journal of organic chemistry.

[57]  G. Wegner,et al.  Proton mobility in oligomer-bound proton solvents: imidazole immobilization via flexible spacers , 2001 .

[58]  M. Brebu,et al.  Polymers with pendent functional groups. V. Thermooxidative and thermal behavior of chloromethylated polysulfones , 2000 .

[59]  Yoshio Kasashima,et al.  Preparation and characterization of novel aromatic polyimides having 4,5-di(1,3-phenylene)imidazole structure , 1998 .

[60]  J. Maier,et al.  Imidazole and pyrazole-based proton conducting polymers and liquids , 1998 .

[61]  K. Kreuer Membrane Materials for PEM-Fuel-Cells: A Microstructural Approach , 1995 .

[62]  N. Kubota,et al.  Combustion Mechanism of Azide Polymer , 1988 .