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Sean Doran

Bio: Sean Doran is an academic researcher from Istanbul Technical University. The author has contributed to research in topics: Copolymer & Methyl methacrylate. The author has an hindex of 6, co-authored 6 publications receiving 621 citations.

Papers
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Journal ArticleDOI
TL;DR: This review paper provides a comprehensive account of the fundamentals and applications of photoinduced electron transfer reactions in polymer synthesis, including traditional photopolymerization methods, namely free radical and cationic polymerizations, and step-growth polymerizations involving electron transfer processes are included.
Abstract: Photochemical reactions, particularly those involving photoinduced electron transfer processes, establish a substantial contribution to the modern synthetic chemistry, and the polymer community has been increasingly interested in exploiting and developing novel photochemical strategies. These reactions are efficiently utilized in almost every aspect of macromolecular architecture synthesis, involving initiation, control of the reaction kinetics and molecular structures, functionalization, and decoration, etc. Merging with polymerization techniques, photochemistry has opened up new intriguing and powerful avenues for macromolecular synthesis. Construction of various polymers with incredibly complex structures and specific control over the chain topology, as well as providing the opportunity to manipulate the reaction course through spatiotemporal control, are one of the unique abilities of such photochemical reactions. This review paper provides a comprehensive account of the fundamentals and applications ...

608 citations

Journal ArticleDOI
TL;DR: Conceptually new one-pot photoinduced sequential click reactions were implemented to yield novel block copolymers with the ability for cell adhesion to furnish desired bioactive blockCopolymer PMMA-b-PCL-NAC.
Abstract: Conceptually new one-pot photoinduced sequential click reactions were implemented to yield novel block copolymers with the ability for cell adhesion. Poly(e-caprolcatone) possessing clickable functional groups at the chain ends, namely α-alkynyl-ω-alkenyl-poly(e-caprolactone) (A-PCL-MA), was prepared by ring-opening polymerization of e-caprolactone using propargyl alcohol in the presence of stannous octoate at 110 °C followed by esterification with methacrylic acid. Azide-functional poly(methyl methacrylate) (PMMA-N3) was prepared independently by atom transfer radical polymerization (ATRP) followed by an azidation process using sodium azide. Finally, A-PCL-MA was reacted with PMMA-N3 and N-acetyl-l-cysteine (NAC) in a one-pot process through photoinduced sequential click reactions to furnish desired bioactive block copolymer (PMMA-b-PCL-NAC). A matrix for cell adhesion was then prepared from the yielded block copolymer PMMA-b-PCL-NAC and cell proliferation on the matrix was measured. Cells from the Vero ...

59 citations

Journal ArticleDOI
TL;DR: In this paper, a photo-induced but photo-initiator-free combined copper-catalyzed azide-alkyne click cycloaddition (CuAAC) and atom-transfer radical polymerization (ATRP) protocol was used to provide a graft copolymer of polystyrene-g-poly(methyl methacrylate) (PSg-PMMA) in desirable conversion and polydispersity.

36 citations

Journal ArticleDOI
TL;DR: In this article, a photo-initiated free-radical-promoted cationic copolymerization of the corresponding monomers using phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO) and diphenyl iodonium hexafluorophosphate (Ph2I+PF6−) as free radical photoinitiator and oxidant, respectively.
Abstract: A novel synthetic strategy involving sequential photoinduced cationic and copper-catalyzed azide–alkyne cycloaddition (CuAAC) click processes for the synthesis of complex macromolecular structures such as side-chain functional polymers, graft copolymers, and organogels is described. In the approach, first a set of copolymers possessing side-chain alkyne or halide functionalities, namely, poly(cyclohexene oxide-co-glycidyl propargyl ether) (P(CHO-co-GPE)), poly(cyclohexene oxide-co-epichlorohydrin) (P(CHO-co-ECH)), and poly(tetrahydrofuran-co-epichlorohydrin) (P(THF-co-ECH)), were synthesized by photoinitiated free-radical-promoted cationic copolymerization of the corresponding monomers using phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO) and diphenyl iodonium hexafluorophosphate (Ph2I+PF6–) as free radical photoinitiator and oxidant, respectively. While P(CHO-co-GPE) readily contained clickable alkyne side-chains, the halide groups of P(THF-co-ECH) were converted to azide groups by conventional a...

25 citations

Journal ArticleDOI
TL;DR: RGD-modified PMMA-b-PCL-NAC as a non-toxic cell proliferation platform was used for selective "integrin αvβ3-mediated cell adhesion and biosensing studies".
Abstract: N-Acetyl-l-cysteine (NAC)-capped poly(methyl methacrylate)-b-polycaprolactone block copolymer (PMMA-b-PCL-NAC) was prepared using the previously described one-pot photoinduced sequential CuAAC/thiol-ene double click procedure. PMMA-b-PCL-NAC had previously shown good applicability as a matrix for cell adhesion of cells from the Vero cell line (African green monkey kidney epithelial). Here, in this work, PMMA-b-PCL-NAC served as an excellent immobilization matrix for biomolecule conjugation. Covalent binding of RGD (R: arginine, G: glycine, and D: aspartic acid) peptide sequence onto the PMMA-b-PCL-NAC-coated surface was performed via EDC chemistry. RGD-modified PMMA-b-PCL-NAC (PMMA-b-PCL-NAC-RGD) as a non-toxic cell proliferation platform was used for selective "integrin αvβ3-mediated cell adhesion and biosensing studies. Both optical and electrochemical techniques were used to monitor the adhesion differences between "integrin αvβ3" receptor positive and negative cell lines on to the designed biofunctional surfaces.

22 citations


Cited by
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Journal ArticleDOI
TL;DR: A comprehensive survey of photo-CRP reactions can be found in this article, where a large number of methods are summarized and further classified into subcategories based on the specific reagents, catalysts, etc., involved.
Abstract: The use of light to mediate controlled radical polymerization has emerged as a powerful strategy for rational polymer synthesis and advanced materials fabrication. This review provides a comprehensive survey of photocontrolled, living radical polymerizations (photo-CRPs). From the perspective of mechanism, all known photo-CRPs are divided into either (1) intramolecular photochemical processes or (2) photoredox processes. Within these mechanistic regimes, a large number of methods are summarized and further classified into subcategories based on the specific reagents, catalysts, etc., involved. To provide a clear understanding of each subcategory, reaction mechanisms are discussed. In addition, applications of photo-CRP reported so far, which include surface fabrication, particle preparation, photoresponsive gel design, and continuous flow technology, are summarized. We hope this review will not only provide informative knowledge to researchers in this field but also stimulate new ideas and applications to further advance photocontrolled reactions.

738 citations

Journal ArticleDOI
20 Feb 2019
TL;DR: The field of 3D printing is continuing its rapid development in both academic and industrial research environments as mentioned in this paper, which offers flexibility over the final properties of the 3D printed materials (such as optical, chemical and mechanical properties) using versatile polymer chemistry.
Abstract: The field of 3D printing is continuing its rapid development in both academic and industrial research environments. The development of 3D printing technologies has opened new implementations in rapid prototyping, tooling, dentistry, microfluidics, biomedical devices, tissue engineering, drug delivery, etc. Among different 3D printing techniques, photopolymerization-based process (such as stereolithography and digital light processing) offers flexibility over the final properties of the 3D printed materials (such as optical, chemical, and mechanical properties) using versatile polymer chemistry. The strategy behind the 3D photopolymerization is based on using monomers/oligomers in liquid state (in the presence of photoinitiators) that can be photopolymerized (via radical or cationic mechanism) upon exposure to light source of different wavelengths (depending on the photoinitiator system). An overview of recent evolutions in the field of photopolymerization-based 3D printing and highlights of novel 3D print...

621 citations

Journal ArticleDOI
TL;DR: This review paper provides a comprehensive account of the fundamentals and applications of photoinduced electron transfer reactions in polymer synthesis, including traditional photopolymerization methods, namely free radical and cationic polymerizations, and step-growth polymerizations involving electron transfer processes are included.
Abstract: Photochemical reactions, particularly those involving photoinduced electron transfer processes, establish a substantial contribution to the modern synthetic chemistry, and the polymer community has been increasingly interested in exploiting and developing novel photochemical strategies. These reactions are efficiently utilized in almost every aspect of macromolecular architecture synthesis, involving initiation, control of the reaction kinetics and molecular structures, functionalization, and decoration, etc. Merging with polymerization techniques, photochemistry has opened up new intriguing and powerful avenues for macromolecular synthesis. Construction of various polymers with incredibly complex structures and specific control over the chain topology, as well as providing the opportunity to manipulate the reaction course through spatiotemporal control, are one of the unique abilities of such photochemical reactions. This review paper provides a comprehensive account of the fundamentals and applications ...

608 citations

Journal Article
TL;DR: This review provides a comprehensive survey of photocontrolled, living radical polymerizations (photo-CRPs), and a large number of methods are summarized and further classified into subcategories based on the specific reagents, catalysts, etc., involved.
Abstract: The use of light to mediate controlled radical polymerization has emerged as a powerful strategy for rational polymer synthesis and advanced materials fabrication. This review provides a comprehensive survey of photocontrolled, living radical polymerizations (photo-CRPs). From the perspective of mechanism, all known photo-CRPs are divided into either (1) intramolecular photochemical processes or (2) photoredox processes. Within these mechanistic regimes, a large number of methods are summarized and further classified into subcategories based on the specific reagents, catalysts, etc., involved. To provide a clear understanding of each subcategory, reaction mechanisms are discussed. In addition, applications of photo-CRP reported so far, which include surface fabrication, particle preparation, photoresponsive gel design, and continuous flow technology, are summarized. We hope this review will not only provide informative knowledge to researchers in this field but also stimulate new ideas and applications to further advance photocontrolled reactions.

602 citations

Journal ArticleDOI
TL;DR: This review, with over 600 references, summarizes the recent applications of photoredox catalysis for organic transformation and polymer synthesis to give an overview of this emerging field to organic and polymer chemists as well as materials scientists.
Abstract: This review, with over 600 references, summarizes the recent applications of photoredox catalysis for organic transformation and polymer synthesis. Photoredox catalysts are metallo- or organo-compounds capable of absorbing visible light, resulting in an excited state species. This excited state species can donate or accept an electron from other substrates to mediate redox reactions at ambient temperature with high atom efficiency. These catalysts have been successfully implemented for the discovery of novel organic reactions and synthesis of added-value chemicals with an excellent control of selectivity and stereo-regularity. More recently, such catalysts have been implemented by polymer chemists to post-modify polymers in high yields, as well as to effectively catalyze reversible deactivation radical polymerizations and living polymerizations. These catalysts create new approaches for advanced organic transformation and polymer synthesis. The objective of this review is to give an overview of this emerging field to organic and polymer chemists as well as materials scientists.

537 citations