A visible-light induced cascade sulfonation/cyclization reaction of 3-allyl-2-arylquinazolinones employing water as an environmentally friendly solvent was revealed.This transition metal-free protocol,using 9-mesityl-...A visible-light induced cascade sulfonation/cyclization reaction of 3-allyl-2-arylquinazolinones employing water as an environmentally friendly solvent was revealed.This transition metal-free protocol,using 9-mesityl-10-methylacridinium perchlorate as the photocatalyst,represents a masterly tactic for the synthesis of sulfonated dihydroisoquinolino[1,2-b]quinazolinones featuring mild conditions,facile operation,and broad substrate scope.展开更多
Cyclo[n]Thiophenes(CnTs)are a distinctive class ofπ-conjugated macrocyclic molecules that have attracted growing attention owing to their structural aesthetics and organic electronic characteristics.However,the devel...Cyclo[n]Thiophenes(CnTs)are a distinctive class ofπ-conjugated macrocyclic molecules that have attracted growing attention owing to their structural aesthetics and organic electronic characteristics.However,the development of CnTs has been largely impeded by inefficient synthetic route.In this work,we employ a bridge strategy using bipyridine as bridge to link two quaterthiophene units resulting in-shaped bicyclosystem.This strain-retaining approach improves the synthesis efficiency of the macrocycles.Two new macrocyclic molecules,(4T-2hexyl-2Me)_(2)-DPBP and(4T-2hexyl)_(2)-DPBP,were successfully synthesized in total yield 17%and 16%,respectively.Single-crystal structure of(4T-2hexyl-2Me)_(2)-DPBP reveals that the bipyridine bridge is orthogonally strapped by two quaterthiophene units.Notably,both compounds exhibit aggregation-induced emission enhancement(AIEE)behavior-an unprecedented feature among CnT-based macrocycles.Theoretical calculations reveal that this AIE phenomenon originates from the restriction of intramolecular motion(RIM)in the aggregated state,which suppresses the non-radiative decay channels.These results demonstrate a generalized strategy for the synthesis of functionalπ-conjugated macrocyclic molecules based fluorescent materials.展开更多
Given the broad applicability of carbazole structural moieties in materials science and medicinal chemistry,significant efforts have been devoted to developing efficient synthetic catalytic methodologies to access thi...Given the broad applicability of carbazole structural moieties in materials science and medicinal chemistry,significant efforts have been devoted to developing efficient synthetic catalytic methodologies to access this valuable scaffold.Catalyzed direct Csp^(2)-H functionalization provides an effective and costefficient approach to synthesizing carbazoles from simple and readily available starting materials,ensuring a promising path characterized by excellent atom and step economy.This review highlights the substantial progress made in the last 10 years in advancing catalytic Csp^(2)-H functionalization techniques for synthesizing carbazoles.展开更多
基金funds from Natural Science Foundation of Guangxi Province(Nos.2023GXNSFBA026304,2023GXNSFDA026063)the Guangxi Science and Technology Base and Special Talents(No.Guike AD20159047).
文摘A visible-light induced cascade sulfonation/cyclization reaction of 3-allyl-2-arylquinazolinones employing water as an environmentally friendly solvent was revealed.This transition metal-free protocol,using 9-mesityl-10-methylacridinium perchlorate as the photocatalyst,represents a masterly tactic for the synthesis of sulfonated dihydroisoquinolino[1,2-b]quinazolinones featuring mild conditions,facile operation,and broad substrate scope.
基金support from the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB0520000)the National Key R&D Program of China(No.2022YFA1203200)+3 种基金National Natural Science Foundation of China(No.52273170)the Youth Innovation Promotion Association of the Chinese Academy of Sciences(No.2021030)Postdoctoral Fellowship Program of CPSF(No.GZC20232735)BMS Junior Fellow of Beijing National Laboratory For molecular Science(No.2023BMS20111).
文摘Cyclo[n]Thiophenes(CnTs)are a distinctive class ofπ-conjugated macrocyclic molecules that have attracted growing attention owing to their structural aesthetics and organic electronic characteristics.However,the development of CnTs has been largely impeded by inefficient synthetic route.In this work,we employ a bridge strategy using bipyridine as bridge to link two quaterthiophene units resulting in-shaped bicyclosystem.This strain-retaining approach improves the synthesis efficiency of the macrocycles.Two new macrocyclic molecules,(4T-2hexyl-2Me)_(2)-DPBP and(4T-2hexyl)_(2)-DPBP,were successfully synthesized in total yield 17%and 16%,respectively.Single-crystal structure of(4T-2hexyl-2Me)_(2)-DPBP reveals that the bipyridine bridge is orthogonally strapped by two quaterthiophene units.Notably,both compounds exhibit aggregation-induced emission enhancement(AIEE)behavior-an unprecedented feature among CnT-based macrocycles.Theoretical calculations reveal that this AIE phenomenon originates from the restriction of intramolecular motion(RIM)in the aggregated state,which suppresses the non-radiative decay channels.These results demonstrate a generalized strategy for the synthesis of functionalπ-conjugated macrocyclic molecules based fluorescent materials.
基金support and funding by the European Union-Next Generation EU under the Italian Ministry of University and Research (MUR) National Innovation Ecosystem (No.ECS00000041-VITALITY and also “Ecosistema TECH4YOU-(Spoke 3-Goal 3.5)MUR is thanked for PRIN-PNRR 2022 project "P2022XKWH7-Circular Waste+3 种基金The University of Perugia is acknowledged for financial support to the university project “Fondo Ricerca di Ateneo,edizione 2022”The National Ph D program in Catalysis coordinated by the University of Perugia is also thankedthe financial supports of key research and development and technology transfer projects of Inner Mongolia Autonomous Region (No.2025KJHZ0008)major special projects of science and technology of Ordos (No.2022EEDSKJZDZX003)。
文摘Given the broad applicability of carbazole structural moieties in materials science and medicinal chemistry,significant efforts have been devoted to developing efficient synthetic catalytic methodologies to access this valuable scaffold.Catalyzed direct Csp^(2)-H functionalization provides an effective and costefficient approach to synthesizing carbazoles from simple and readily available starting materials,ensuring a promising path characterized by excellent atom and step economy.This review highlights the substantial progress made in the last 10 years in advancing catalytic Csp^(2)-H functionalization techniques for synthesizing carbazoles.
