Year |
Citation |
Score |
2023 |
Scanga RA, Shahrokhinia A, Borges J, Sarault SH, Ross MB, Reuther JF. Asymmetric Polymerization-Induced Crystallization-Driven Self-Assembly of Helical, Rod-Coil Poly(aryl isocyanide) Block Copolymers. Journal of the American Chemical Society. 145: 6319-6329. PMID 36913666 DOI: 10.1021/jacs.2c13354 |
0.355 |
|
2020 |
Wechsler ME, Dang HKHJ, Dahlhauser SD, Simmonds SP, Reuther JF, Wyse JM, VandeWalle AN, Anslyn EV, Peppas NA. Nanogel receptors for high isoelectric point protein detection: influence of electrostatic and covalent polymer-protein interactions. Chemical Communications (Cambridge, England). PMID 32364214 DOI: 10.1039/D0Cc02200D |
0.347 |
|
2020 |
Sun X, Chwatko M, Lee DH, Bachman JL, Reuther JF, Lynd NA, Anslyn EV. Chemically Triggered Synthesis, Remodeling, and Degradation of Soft Materials. Journal of the American Chemical Society. PMID 32011873 DOI: 10.1021/Jacs.9B12122 |
0.391 |
|
2018 |
Hernandez ET, Rogelio Escamilla P, Kwon SY, Partridge J, McVeigh M, Rivera S, Reuther JF, Anslyn EV. 2,2'-Bipyridine and hydrazide containing peptides for cyclization and complex quaternary structural control. New Journal of Chemistry = Nouveau Journal De Chimie. 42: 8577-8582. PMID 30386131 DOI: 10.1039/C8Nj00184G |
0.304 |
|
2018 |
Reuther JF, Dahlhauser SD, Anslyn EV. Tunable Orthogonal Reversible Covalent (TORC) Bonds: Dynamic Chemical Control over Molecular Assembly. Angewandte Chemie (International Ed. in English). PMID 30098086 DOI: 10.1002/Anie.201808371 |
0.356 |
|
2018 |
Reuther JF, Goodrich AC, Escamilla PR, Lu TA, Del Rio V, Davies BW, Anslyn EV. A Versatile Approach to Noncanonical, Dynamic Covalent Single and Multi-Loop Peptide Macrocycles for Enhancing Antimicrobial Activity. Journal of the American Chemical Society. PMID 29466660 DOI: 10.1021/Jacs.8B00046 |
0.323 |
|
2018 |
Reuther JF, Dees JL, Kolesnichenko IV, Hernandez ET, Ukraintsev DV, Guduru R, Whiteley M, Anslyn EV. Dynamic covalent chemistry enables formation of antimicrobial peptide quaternary assemblies in a completely abiotic manner. Nature Chemistry. 10: 45-50. PMID 29256509 DOI: 10.1038/Nchem.2847 |
0.343 |
|
2017 |
Campos R, Reuther JF, Mammoottil NR, Novak BM. Solid State Sensing of Nonpolar VOCs Using the Bistable Expansion and Contraction of Helical Polycarbodiimides Macromolecules. 50: 4927-4934. DOI: 10.1021/Acs.Macromol.7B01095 |
0.776 |
|
2017 |
Siriwardane DA, Kulikov O, Reuther JF, Novak BM. Rigid, Helical Arm Stars through Living Nickel Polymerization of Carbodiimides Macromolecules. 50: 832-840. DOI: 10.1021/Acs.Macromol.6B02456 |
0.798 |
|
2017 |
Mammoottil NR, Reuther JF, Siriwardane DA, Kulikov OV, Novak BM. Developments in synthesis, characterization, and self-assembly of polycarbodiimide systems Journal of Polymer Science Part a: Polymer Chemistry. 55: 2915-2934. DOI: 10.1002/Pola.28583 |
0.814 |
|
2015 |
Reuther JF, Siriwardane DA, Campos R, Novak BM. Solvent Tunable Self-Assembly of Amphiphilic Rod-Coil Block Copolymers with Chiral, Helical Polycarbodiimide Segments: Polymeric Nanostructures with Variable Shapes and Sizes Macromolecules. 48: 6890-6899. DOI: 10.1021/Acs.Macromol.5B01564 |
0.755 |
|
2015 |
Reuther JF, Siriwardane DA, Kulikov OV, Batchelor BL, Campos R, Novak BM. Facile synthesis of rod-coil block copolymers with chiral, helical polycarbodiimide segments via postpolymerization CuAAC "click" coupling of functional end groups Macromolecules. 48: 3207-3216. DOI: 10.1021/Acs.Macromol.5B00453 |
0.721 |
|
2015 |
Kulikov OV, Siriwardane DA, Reuther JF, McCandless GT, Sun HJ, Li Y, Mahmood SF, Sheiko SS, Percec V, Novak BM. Characterization of Fibrous Aggregated Morphologies and Other Complex Architectures Self-Assembled from Helical Alkyne and Triazole Polycarbodiimides (R)- and (S)-Families in the Bulk and Thin Film Macromolecules. 48: 4088-4103. DOI: 10.1021/Acs.Macromol.5B00407 |
0.743 |
|
2014 |
Merten C, Reuther JF, DeSousa JD, Novak BM. Identification of the specific, shutter-like conformational reorientation in a chiroptical switching polycarbodiimide by VCD spectroscopy. Physical Chemistry Chemical Physics : Pccp. 16: 11456-60. PMID 24800924 DOI: 10.1039/C4Cp01226G |
0.785 |
|
2014 |
Bhatt MP, Du J, Rainbolt EA, Pathiranage TMSK, Huang P, Reuther JF, Novak BM, Biewer MC, Stefan MC. A semiconducting liquid crystalline block copolymer containing regioregular poly(3-hexylthiophene) and nematic poly(n-hexyl isocyanate) and its application in bulk heterojunction solar cells Journal of Materials Chemistry A. 2: 16148-16156. DOI: 10.1039/C4Ta02852J |
0.689 |
|
2014 |
Merten C, Reuther JF, Desousa JD, Novak BM. Identification of the specific, shutter-like conformational reorientation in a chiroptical switching polycarbodiimide by VCD spectroscopy Physical Chemistry Chemical Physics. 16: 11456-11460. DOI: 10.1039/c4cp01226g |
0.746 |
|
2014 |
Reuther JF, Bhatt MP, Tian G, Batchelor BL, Campos R, Novak BM. Controlled living polymerization of carbodiimides using versatile, air-stable nickel(II) initiators: Facile incorporation of helical, rod-like materials Macromolecules. 47: 4587-4595. DOI: 10.1021/Ma5009429 |
0.727 |
|
2013 |
Reuther JF, Novak BM. Evidence of entropy-driven bistability through (15)N NMR analysis of a temperature- and solvent-induced, chiroptical switching polycarbodiimide. Journal of the American Chemical Society. 135: 19292-303. PMID 24313274 DOI: 10.1021/Ja4098803 |
0.687 |
|
2013 |
Reuther JF, Novak BM. Evidence of entropy-driven bistability through 15N NMR analysis of a temperature- and solvent-induced, chiroptical switching polycarbodiimide Journal of the American Chemical Society. 135: 19292-19303. DOI: 10.1021/ja4098803 |
0.557 |
|
2012 |
Budhathoki-Uprety J, Reuther JF, Novak BM. Determining the regioregularity in alkyne polycarbodiimides and their orthogonal modification of side chains to yield perfectly alternating functional polymers Macromolecules. 45: 8155-8165. DOI: 10.1021/Ma301639M |
0.813 |
|
2012 |
Reuther JF, Desousa JD, Novak BM. Direct probing of regioregularity for polycarbodiimide systems via 15N NMR analysis Macromolecules. 45: 7719-7728. DOI: 10.1021/Ma301448B |
0.783 |
|
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