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Inside Cover: Stapled Peptides with γ‐Methylated Hydrocarbon Chains for the Estrogen Receptor/Coactivator Interaction (Angew. Chem. Int. Ed. 13/2016)
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Shijing Cheng Mingqiang Zhang Tianyu Wu Sean T. Hemp Brian D. Mather Robert B. Moore Timothy E. Long 《Journal of polymer science. Part A, Polymer chemistry》2012,50(1):166-173
Copolymers of n‐butyl acrylate and phosphonium ionic liquid monomers possessing various alkyl substituents and counterions were synthesized through a combination of conventional free radical copolymerization and anion exchange. Differential scanning calorimetry and dynamic mechanical analysis provided the thermal and mechanical properties of these phosphonium cation‐containing random copolymers. Factors including alkyl chain length of phosphonium substituents, counterion type, as well as ionic concentration significantly influenced the association of phosphonium cations. Phosphonium ionomers with trialkyl substituents on phosphonium cations did not display the characteristic small‐angle X‐ray scattering peak, suggesting the absence of ionic clusters. However, low q peaks in wide‐angle X‐ray diffraction was indicative of significant concentration fluctuations wherein the ionic monomeric units associated. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
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Hans Eliot Edling Matthew Vincent Herv Marand Samantha J. Talley Kevin Barr Robert B. Moore S. Richard Turner 《Journal of Polymer Science.Polymer Physics》2019,57(15):973-980
Structurally rigid copolyester thermoplastics were synthesized from 1,4‐cyclohexanedimethanol and the diesters dimethyl biphenyl‐4,4′‐dicarboxylate and dimethyl 2,6‐naphthalenedicarboxylate (DMN) via conventional melt transesterification. Conventional differential scanning calorimetry (CDSC) showed all compositions to exhibit multiple endotherms upon heating. Wide‐angle X‐ray diffraction analysis showed copolyester compositions to exhibit the crystalline structure of either the homopolyester Poly(1,4‐cyclohexylenedimethylene 2,6‐naphthalate) (PCN) or the homopolyester Poly(1,4‐cyclohexylenedimethylene 4,4′‐bibenzoate) (PCB), but not both simultaneously. Further thermal analysis using CDSC and fast DSC investigated the origin of the multiple endotherm behavior. While three endotherms are observed for low heating rates, the upper two endotherms appear to merge at heating rates about 1–5 °C s?1 and a single endotherm remains above heating rates about 10–50 °C s?1. While the behavior of the upper two endotherms is undeniably consistent with the mechanism of melting–recrystallization–remelting (MRR), we suggest that the low endotherm is likely associated with the melting of constrained secondary crystals, although MRR effects cannot be ruled out. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 973–980 相似文献
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Nitrite reduction by a copper complex featuring a proton-responsive tripodal ligand is demonstrated. Gaseous nitric oxide was confirmed as the sole NOX by-product in quantitative yield. DFT calculations predict that nitrite reduction occurs via a proton and electron transfer process mediated by the ligand. The reported mechanism parallels nitrite reduction by copper nitrite reductase. 相似文献
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Timothy P. Moneypenny II Huiying Liu Anna Yang Ian D. Robertson Jeffrey S. Moore 《Journal of polymer science. Part A, Polymer chemistry》2017,55(18):2935-2948
Alkene metathesis has proven to be a powerful method for carbon carbon bond formation, particularly in the field of polymer and materials science. The availability of various tailor-made catalysts not only enables the synthesis of well-defined polymers but facilitates the development of functional, stimuli–responsive materials. This highlight, dedicated to Professor Robert Grubbs on his 75th birthday, focuses on the various research efforts in our group utilizing both alkene and alkyne metatheses and the interesting materials derived from them. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2935–2948 相似文献