Abstract:in 2006, where he conducted research with Professor Dhandapani Venkataraman of the Chemistry Department and Professor Todd Emrick of the Polymer Science and Engineering Department. He came to UCSB to pursue a Ph.D. in the Hawker group in 2006, where his research is focused on both smallmolecule and polymer synthesis for solar cells and other energy capture and storage applications.
“…From the several proposed click type reactions in the literature [326][327], two of them received much attention within the polymer society: Cu(I) catalyzed azide-alkyne cycloaddition (CuAAC) [328][329][330][331][332] and the addition of a thiyl radical to olefins (thiol-ene and thiol-yne) [230,[333][334] (Scheme 2).…”
Section: General Particle Functionalizationmentioning
“…From the several proposed click type reactions in the literature [326][327], two of them received much attention within the polymer society: Cu(I) catalyzed azide-alkyne cycloaddition (CuAAC) [328][329][330][331][332] and the addition of a thiyl radical to olefins (thiol-ene and thiol-yne) [230,[333][334] (Scheme 2).…”
Section: General Particle Functionalizationmentioning
Section: Materials and General Protocolsmentioning
confidence: 99%
“…Poly(Glu-co-Cys) is a biomimetic polypeptide of phytochelatins, which effectively capture and remove heavy metals in natural plants. Poly(Glu-co-Cys) with a composition of Glu/Cys = 53/47 exhibited the ability to sequester divalent heavy metal ions, similar to the uniform sequence peptide (Glu-Cys) 4 -Gly, a phytochelatin analog. [106] These results suggest that cysteine-containing polypeptides can be used as a potential sorbent for toxic heavy metals in wastewater and polluted soils.…”
Section: Hydrophilic Polypeptides For Use As Functional Materialsmentioning
confidence: 99%
“…The wide range of protein functionality has inspired intense interest in the possibility of using polypeptide materials in various fields, including biomedicine, pharmaceuticals, and tissue engineering. [1][2][3][4][5][6][7] In particular, specific functional motifs of polypeptides, which are represented by short polypeptide fragments in their sequences, are extracted to exploit their specific functions. [3,8] sequentially controlled polypeptides.…”
Polypeptides inspired by the natural functional and structural proteins present in living systems are promising materials for various fields in terms of their versatile functionality and physical properties. Designing and synthesizing mimetic sequences of specific peptide motifs in proteins are important for exploring the functionality of natural proteins. Chemoenzymatic polymerization, which utilizes aminolysis (i.e., the reverse reaction of hydrolysis catalyzed by proteases), is a useful technique for synthesizing artificial polypeptide materials and has several advantages, including facile synthesis protocols, environmental friendliness, scalability, and atom economy. In this review, recent progress in chemoenzymatic polypeptide synthesis for the production of functional and structural materials for various applications is summarized in conjunction with the current status of technical challenges in the field.
“…[40] The "click" chemistry toolbox includes, for example, ring-opening reactions, thiolene addition, and CuAAC reactions. [41][42][43][44][45] In particular, the CuAAC reaction can be performed under physiological conditions and has found numerous applications in the field of surface chemistry. [45] The upcoming use of silicon-based materials has logically initiated a growing interest in the post-modification of SiÀC-bound organic monolayers by using the click reaction.…”
Copper-catalyzed azide-alkyne cycloaddition (CuAAC), combined with the chemical stability of the SiÀC-bound organic layer, serves as an efficient tool for the modification of silicon substrates, particularly for the immobilization of complex biomolecules. This review covers recent advances in the preparation of alkynyl-or azido-terminated "clickable" platforms on non-oxidized silicon and their further derivatization by means of the CuAAC reaction. The exploitation of these "click"-functionalized organic thin films as model surfaces to study many biological events was also addressed, as they are directly relevant to the on-going effort of creating siliconbased molecular electronics and chemical/biomolecular sensors.
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