The development of highly effective photosensitizers(PSs)based on supramolecular coordination complexes(SCCs)is highly appealing in supramolecular chemistry,materials science,and biology.SCCs offer promising platforms...The development of highly effective photosensitizers(PSs)based on supramolecular coordination complexes(SCCs)is highly appealing in supramolecular chemistry,materials science,and biology.SCCs offer promising platforms for incorporating multiple PSs and other functional units into their well-defined structures,allowing for precise control over the number and distribution of these components.In this study,we present an efficient and straightforward method for modulating the photosensitization process of PSs derived from a family of BF_(2)-chelated dipyrromethene(BODIPY)-containing Pt(Ⅱ)metallacycles by varying pre-designed Pt(Ⅱ)acceptors.By utilizing different Pt(Ⅱ)acceptors with varying Pt atom configurations and degrees ofπ-conjugated organic moieties,we observed tunable characteristics in the photosensitization process and singlet oxygen(^(1)O_(2))generation efficiency of these targeted metallacycles.Furthermore,we successfully conducted the visible-light-driven oxidative coupling of various amines to imines,catalyzed by the prepared metallacycle PSs.This study offers a novel approach for fabricating efficient PSs based on SCCs,featuring tunable photosensitization efficiency and excellent photocatalytic reactivity,while providing new insights into the preparation of effective PSs.展开更多
Bacterial infections pose a significant threat to human health and entail substantial economic losses.Due to the broad-spectrum antibacterial effect and low susceptibility to drug resistance,photodynamic therapy(PDT),...Bacterial infections pose a significant threat to human health and entail substantial economic losses.Due to the broad-spectrum antibacterial effect and low susceptibility to drug resistance,photodynamic therapy(PDT),a nontraditional antibacterial approach,has garnered a lot of attention.In PDT,the selection of photosensitizer(PS)is crucial because it directly affects the efficiency and safety of the treatment.As a versatile fluorophore,the advantages of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene(BODIPY)used as a PS for antibacterial PDT are mainly reflected in its high quantum yield of singlet oxygen,easy modification,and exceptional photostability.Through strategic chemical modifications of the BODIPY structures,it is possible to enhance their photodynamic antibacterial activity and refine their selectivity for bacterial killing.This review focuses on the application of BODIPY-based PSs for treating bacterial infections.According to the design strategies of photodynamic antibacterial materials incorporating BODIPY,a variety of representative therapeutic agents having emerged in recent years are classified and discussed,aiming to offer insights for future research and development in this field.展开更多
We compared a range of BODIPY dimer derivatives without installing blocking groups by optimizing geometry structures and analyzing energies,frontier mo-lecular orbitals,Chole&Cele map,electron density difference,s...We compared a range of BODIPY dimer derivatives without installing blocking groups by optimizing geometry structures and analyzing energies,frontier mo-lecular orbitals,Chole&Cele map,electron density difference,spin-orbit coupling(SOC)matrix and decay rate constants from excited states.The dihedral angles of theβ-β-linked BODIPY dimer and theα-α-linked BODIPY dimer tend to flatten in the T_(1)state,which is detrimental to the occurrence of the intersystem crossing(ISC).Conversely,the dihedral angle of the meso-β-linked BODIPY dimer,the meso-meso-linked BODIPY dimer andα-γ-linked BODIPY dimer is within the range of 125°-143°in the T_(1)state,facilitating ISC and the generation of singlet oxygen.Notably,the transition from S1 to S0 involving lowest unoccupied mo-lecular orbital to highest occupied molecular orbital with long-wavelength emis-sion and moderate oscillator strength underpins the remarkable long emission peaks observed experimentally forα-γ-linked BODIPY dimer.Moreover,the apparent SOC matrix enhances the ISC process,resulting in a respectable effi-ciency in generating singlet oxygen for this dimer.In meso-β-linked BODIPY,meso-meso-linked BODIPY,andα-γ-linked BODIPY,the S_(1)→T_(1)process is characterized by a significant charge transfer,specifically transitioning from the^(1)CT state to the^(3)LE state,indicative of a spin-orbit charge transfer ISC(SOCTISC)mechanism.The ability to regulate the photosensitivity of BODIPY dimers by adjusting the dihedral angle between the two units in the T_(1)state unveils new avenues for designing high-performance photosensitizers for both therapeutic and imaging applications.展开更多
基金the financial support by the National Natural Science Foundation of China(Nos.22301081,22301269 and 22401096)China Postdoctoral Science Foundation(No.2023M731095)+4 种基金the Shanghai Frontiers Science Center for Molecular Intelligent Synthesesthe Fundamental Research Funds for the Central UniversitiesYoung Talent Fund of Association for Science and Technology in Shaanxi,China(No.20240628)Scientific Research Program Funded by Education Department of Shaanxi Provincial Government(No.23JK0752)Foundation of Yulin Association for Science and Technology(No.20230512)。
文摘The development of highly effective photosensitizers(PSs)based on supramolecular coordination complexes(SCCs)is highly appealing in supramolecular chemistry,materials science,and biology.SCCs offer promising platforms for incorporating multiple PSs and other functional units into their well-defined structures,allowing for precise control over the number and distribution of these components.In this study,we present an efficient and straightforward method for modulating the photosensitization process of PSs derived from a family of BF_(2)-chelated dipyrromethene(BODIPY)-containing Pt(Ⅱ)metallacycles by varying pre-designed Pt(Ⅱ)acceptors.By utilizing different Pt(Ⅱ)acceptors with varying Pt atom configurations and degrees ofπ-conjugated organic moieties,we observed tunable characteristics in the photosensitization process and singlet oxygen(^(1)O_(2))generation efficiency of these targeted metallacycles.Furthermore,we successfully conducted the visible-light-driven oxidative coupling of various amines to imines,catalyzed by the prepared metallacycle PSs.This study offers a novel approach for fabricating efficient PSs based on SCCs,featuring tunable photosensitization efficiency and excellent photocatalytic reactivity,while providing new insights into the preparation of effective PSs.
文摘Bacterial infections pose a significant threat to human health and entail substantial economic losses.Due to the broad-spectrum antibacterial effect and low susceptibility to drug resistance,photodynamic therapy(PDT),a nontraditional antibacterial approach,has garnered a lot of attention.In PDT,the selection of photosensitizer(PS)is crucial because it directly affects the efficiency and safety of the treatment.As a versatile fluorophore,the advantages of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene(BODIPY)used as a PS for antibacterial PDT are mainly reflected in its high quantum yield of singlet oxygen,easy modification,and exceptional photostability.Through strategic chemical modifications of the BODIPY structures,it is possible to enhance their photodynamic antibacterial activity and refine their selectivity for bacterial killing.This review focuses on the application of BODIPY-based PSs for treating bacterial infections.According to the design strategies of photodynamic antibacterial materials incorporating BODIPY,a variety of representative therapeutic agents having emerged in recent years are classified and discussed,aiming to offer insights for future research and development in this field.
基金financially supported by the Fundamental Research Funds for the Central Universities(DUT20RC(3)076)Natural Science Foundation of Liaoning Province(2020-MS-293).Thanks Shuoqi Sun from HZWTECH for help and discussions regarding this study.
文摘We compared a range of BODIPY dimer derivatives without installing blocking groups by optimizing geometry structures and analyzing energies,frontier mo-lecular orbitals,Chole&Cele map,electron density difference,spin-orbit coupling(SOC)matrix and decay rate constants from excited states.The dihedral angles of theβ-β-linked BODIPY dimer and theα-α-linked BODIPY dimer tend to flatten in the T_(1)state,which is detrimental to the occurrence of the intersystem crossing(ISC).Conversely,the dihedral angle of the meso-β-linked BODIPY dimer,the meso-meso-linked BODIPY dimer andα-γ-linked BODIPY dimer is within the range of 125°-143°in the T_(1)state,facilitating ISC and the generation of singlet oxygen.Notably,the transition from S1 to S0 involving lowest unoccupied mo-lecular orbital to highest occupied molecular orbital with long-wavelength emis-sion and moderate oscillator strength underpins the remarkable long emission peaks observed experimentally forα-γ-linked BODIPY dimer.Moreover,the apparent SOC matrix enhances the ISC process,resulting in a respectable effi-ciency in generating singlet oxygen for this dimer.In meso-β-linked BODIPY,meso-meso-linked BODIPY,andα-γ-linked BODIPY,the S_(1)→T_(1)process is characterized by a significant charge transfer,specifically transitioning from the^(1)CT state to the^(3)LE state,indicative of a spin-orbit charge transfer ISC(SOCTISC)mechanism.The ability to regulate the photosensitivity of BODIPY dimers by adjusting the dihedral angle between the two units in the T_(1)state unveils new avenues for designing high-performance photosensitizers for both therapeutic and imaging applications.
