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Creators/Authors contains: "Zholdassov, Yerzhan S."

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  1. Mechanical activation of reactions can reduce significantly the amounts of solvent and energy required to form covalent organic bonds.

     
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    Free, publicly-accessible full text available March 12, 2025
  2. Free, publicly-accessible full text available December 19, 2024
  3. A modified atomic force microscope is used to probe activation effects that may accelerate reactions in a ball mill. 
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  4. Hypersurface photolithography (HP) is a printing method for fabricating structures and patterns composed of soft materials bound to solid surfaces and with ∼1 micrometer resolution in the x , y , and z dimensions. This platform leverages benign, low intensity light to perform photochemical surface reactions with spatial and temporal control of irradiation, and, as a result, is particularly useful for patterning delicate organic and biological material. In particular, surface-initiated controlled radical polymerizations can be leveraged to create arbitrary polymer and block-copolymer brush patterns. Here we will review advances in instrumentation architectures that have made these hypersurfaces possible, and the investigations and development of surface-based organic chemistry and grafted-from photopolymerizations that have arisen through these investigations. Over the course of this discussion, we describe specific applications that have benefited from HP. By combining organic chemistry with the instrumentation developed, HP has ushered in a new era of surface chemistry that will lead to new fundamental science and previously unimaginable technologies. 
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  5. Abstract

    A photochemical printer, equipped with a digital micromirror device (DMD), leads to the rapid elucidation of the kinetics of the surface‐initiated atom‐transfer radical photopolymerization ofN,N‐dimethylacrylamide (DMA) andN‐isopropylacrylamide (NIPAM) monomers. This effort reveals conditions where polymer brushes of identical heights can be grown from each monomer. With these data, hidden images are created that appear upon heating the substrate above the lower critical solution temperature (LCST) of polyNIPAM. By introducing a third monomer, methacryloxyethyl thiocarbamoyl rhodamine B, a second, orthogonal image appears upon UV‐irradiation. With these studies, it is shown how a new photochemical printer accelerates discovery, creates arbitrary patterns, and addresses long‐standing problems in brush polymer and surface chemistry. With this technology in hand a new method is demonstrated to encrypt data within hypersurfaces.

     
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  6. Abstract

    We report a novel glycan array architecture that binds the mannose‐specific glycan binding protein, concanavalin A (ConA), with sub‐femtomolar avidity. A new radical photopolymerization developed specifically for this application combines the grafted‐from thiol–(meth)acrylate polymerization with thiol–ene chemistry to graft glycans to the growing polymer brushes. The propagation of the brushes was studied by carrying out this grafted‐to/grafted‐from radical photopolymerization (GTGFRP) at >400 different conditions using hypersurface photolithography, a printing strategy that substantially accelerates reaction discovery and optimization on surfaces. The effect of brush height and the grafting density of mannosides on the binding of ConA to the brushes was studied systematically, and we found that multivalent and cooperative binding account for the unprecedented sensitivity of the GTGFRP brushes. This study further demonstrates the ease with which new chemistry can be tailored for an application as a result of the advantages of hypersurface photolithography.

     
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  7. Abstract

    We report a novel glycan array architecture that binds the mannose‐specific glycan binding protein, concanavalin A (ConA), with sub‐femtomolar avidity. A new radical photopolymerization developed specifically for this application combines the grafted‐from thiol–(meth)acrylate polymerization with thiol–ene chemistry to graft glycans to the growing polymer brushes. The propagation of the brushes was studied by carrying out this grafted‐to/grafted‐from radical photopolymerization (GTGFRP) at >400 different conditions using hypersurface photolithography, a printing strategy that substantially accelerates reaction discovery and optimization on surfaces. The effect of brush height and the grafting density of mannosides on the binding of ConA to the brushes was studied systematically, and we found that multivalent and cooperative binding account for the unprecedented sensitivity of the GTGFRP brushes. This study further demonstrates the ease with which new chemistry can be tailored for an application as a result of the advantages of hypersurface photolithography.

     
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