Abstract:As one type of important species in chemistry the instability of carbocations remains a longstanding issue in view of the electron-deficiency feature. Herein we report light-triggered on-demand creation of carbocations...
“…18a). 148 Detailed mechanistic studies suggest light-induced promotion of aromaticity as the stabilizing force, and nucleus-independent chemical shift (NICS) calculations gave NICS(1) zz values of 11.6 (antiaromatic) and −7.7 (aromatic) ppm on the five-membered cyclic acyliminium ion for o -40A and c -40A . The use of in situ created and isolated carbocations as Lewis acid catalysts was validated with aromatic electrophilic substitution and ring-opening polymerization reactions (Fig.…”
Section: Photoswitchable Dual Reactivity Based DCCmentioning
Dynamic covalent chemistry (DCC) focuses on reversible formation, breakage, and exchange of covalent bonds and assemblies, setting a bridge between irreversible organic synthesis and supramolecular chemistry and finding wide utility....
“…18a). 148 Detailed mechanistic studies suggest light-induced promotion of aromaticity as the stabilizing force, and nucleus-independent chemical shift (NICS) calculations gave NICS(1) zz values of 11.6 (antiaromatic) and −7.7 (aromatic) ppm on the five-membered cyclic acyliminium ion for o -40A and c -40A . The use of in situ created and isolated carbocations as Lewis acid catalysts was validated with aromatic electrophilic substitution and ring-opening polymerization reactions (Fig.…”
Section: Photoswitchable Dual Reactivity Based DCCmentioning
Dynamic covalent chemistry (DCC) focuses on reversible formation, breakage, and exchange of covalent bonds and assemblies, setting a bridge between irreversible organic synthesis and supramolecular chemistry and finding wide utility....
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