Name: 3-Bromopropan-1-olIn 2021 ,《How to Choose a Secondary Interaction to Improve Stretchability of Associative Polymers?》 was published in Macromolecules (Washington, DC, United States). The article was written by Yang, Huanhuan; Wu, Shilong; Chen, Quan. The article contains the following contents:
This study focuses on the stretchability of brittle ionomers after introducing three types of hydrogen bonds, i.e., dual, triple, and quadruple hydrogen bonds. The introduction of dual or triple hydrogen bonds that are weaker than the ionic association improves the stretchability, and better improvement has been achieved for the triple hydrogen bonds. In comparison, the introduction of quadruple hydrogen bonds that are equally strong as the ionic association does not show this type of improvement. This result strongly indicates that there is an optimized strength ratio between the first (the stronger ionic) network and the secondary (the weaker hydrogen-bonding) network, i.e., the secondary network should be considerably weaker but still not too weaker than the first network. When this condition is satisfied, continuous dissociation and association of the secondary network weaken the chain retraction after the strain-induced breakup of the first network, thereby suppressing the formation of defects or microscopic cracks that potentially grow into the macroscopic fracture. In addition to this study using 3-Bromopropan-1-ol, there are many other studies that have used 3-Bromopropan-1-ol(cas: 627-18-9Name: 3-Bromopropan-1-ol) was used in this study.
3-Bromopropan-1-ol(cas: 627-18-9) is used in the synthesis of fluorescent halide-sensitive quinolinium dyes, chiral, quaternary prolines through cyclization of quaternary amino acids and molten salt-polymers. It is utilized for the study of micellar media and in microemulsions based on cationic or a nonionic surfactant by reacting with phenols.Name: 3-Bromopropan-1-ol
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