Three multi-fluorous-carried anions-based ionic copolymers(ICs)including(fluorosulfonyl)imide(FSI-),(trifluorometha-nesulfonyl)imide(TFSI-)and hexafluorophosphate anions(PF6-)(IC[FSI-]),poly[1,1'-(butane-1,4-diyl)...Three multi-fluorous-carried anions-based ionic copolymers(ICs)including(fluorosulfonyl)imide(FSI-),(trifluorometha-nesulfonyl)imide(TFSI-)and hexafluorophosphate anions(PF6-)(IC[FSI-]),poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bis(fluorosulfonyl)amide](IC[TFSI-]),poly{1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bis[(trifluoromethyl)sulfonyl]-amide}(IC[PF6-]),poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bishexafluorophosphate]were synthesized with a simple ionic exchange method by using amphiphilic poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bisbromide](IC[Br-])as the intermediate ionic polymer.The chemical srutrcures of the target ICs were characterized by nuclear magnetic resonance(NMR)spectroscopy and Fourier-transform infrared spectroscopy(FTIR).It is shown that the target ICs could be spontaneously adsorbed on copper surface in N,N-dimethflormamide(DMF),and the tight adsorption films were formed on metal surface.The contacting angles suggest that the formed adsorption layers of target ICs on copper surface were characterized with hydrophobic nature.Furthermore,the target ICs-copper chemistry bonding was confirmed by various means.The electrochemistry analysis showed that the target ICs adsorption layers could prevent from copper corrosion in H2SO4solution efficiently,and the maximal anticorrosion efficiency was over 95%at 0.100 g/L.In particular,the target ICs showed 85%or above anticorrosion efficiency for copper at a low concentration of 0.025 g/L,which was greater than the intermediate polymer IC[Br-].In addition,an insight of mixed chemisorption and physisorption of the target ICs on metal surface was analyzed and discussed.展开更多
To study the structure-activity relationship of endomorphins (EMs), the action of opioid receptor binding (AORB), analgesic activity and vasodilator effects of EMs and their eight analogs were investigated, which were...To study the structure-activity relationship of endomorphins (EMs), the action of opioid receptor binding (AORB), analgesic activity and vasodilator effects of EMs and their eight analogs were investigated, which were prepared by rationally replacing the 2-/3-amino acid (Aa) of EMs. The results showed: (i) The 2-Aa was comparatively more related to the selectivity of EMs while the 3-Aa to their affinity; (ii) the analgesia and vasodilatation of EMs and their analogs were not completely dictated by their AORB (in vitro), the action of [D-Pro2]EM-2 was unusual; (iii) EMs lost their analgesia in the central nervous system and their vasodilatation in the circulatory system with different mechanisms; the former was due to the degradation of some peptidase, and the latter possibly due to the feedback inhibition.展开更多
基金This work was supported by the National Natural Science Foundation of China(Nos.21376282,21676035,21878029)the Project of the Chongqing Science and Technology Commission,China(No.2022NSCQ-MSX1298)+4 种基金the Graduate Student Research Innovation Project,Chongqing University,China(No.CYB18046)the Natural Science Foundation of Chongqing,China(No.cstc2019jcyj-msxmX0663)the Science and Technology Research Program of Chongqing Municipal Education Commission,China(Nos.KJQN201904102,KJQN202004104)the Beibei Scientific and Technological Program Project of China(No.2019-2)the Scientific Research Program of Chongqing Youth Vocational&Technical College,China(No.CQY2019KYY04).
文摘Three multi-fluorous-carried anions-based ionic copolymers(ICs)including(fluorosulfonyl)imide(FSI-),(trifluorometha-nesulfonyl)imide(TFSI-)and hexafluorophosphate anions(PF6-)(IC[FSI-]),poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bis(fluorosulfonyl)amide](IC[TFSI-]),poly{1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bis[(trifluoromethyl)sulfonyl]-amide}(IC[PF6-]),poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bishexafluorophosphate]were synthesized with a simple ionic exchange method by using amphiphilic poly[1,1'-(butane-1,4-diyl)bis(3-pentyl-1H-imidazol-3-ium)bisbromide](IC[Br-])as the intermediate ionic polymer.The chemical srutrcures of the target ICs were characterized by nuclear magnetic resonance(NMR)spectroscopy and Fourier-transform infrared spectroscopy(FTIR).It is shown that the target ICs could be spontaneously adsorbed on copper surface in N,N-dimethflormamide(DMF),and the tight adsorption films were formed on metal surface.The contacting angles suggest that the formed adsorption layers of target ICs on copper surface were characterized with hydrophobic nature.Furthermore,the target ICs-copper chemistry bonding was confirmed by various means.The electrochemistry analysis showed that the target ICs adsorption layers could prevent from copper corrosion in H2SO4solution efficiently,and the maximal anticorrosion efficiency was over 95%at 0.100 g/L.In particular,the target ICs showed 85%or above anticorrosion efficiency for copper at a low concentration of 0.025 g/L,which was greater than the intermediate polymer IC[Br-].In addition,an insight of mixed chemisorption and physisorption of the target ICs on metal surface was analyzed and discussed.
基金This work was supported by the National Natural Science Foundation of China (Grant No. 20072014) the Teaching and Research Award Program for Outstanding Young Teachers in Higher Education Institutions of MOE of China Gansu Provincial Key Science and
文摘To study the structure-activity relationship of endomorphins (EMs), the action of opioid receptor binding (AORB), analgesic activity and vasodilator effects of EMs and their eight analogs were investigated, which were prepared by rationally replacing the 2-/3-amino acid (Aa) of EMs. The results showed: (i) The 2-Aa was comparatively more related to the selectivity of EMs while the 3-Aa to their affinity; (ii) the analgesia and vasodilatation of EMs and their analogs were not completely dictated by their AORB (in vitro), the action of [D-Pro2]EM-2 was unusual; (iii) EMs lost their analgesia in the central nervous system and their vasodilatation in the circulatory system with different mechanisms; the former was due to the degradation of some peptidase, and the latter possibly due to the feedback inhibition.
