Partial genetically encoded 4-hy-droxybenzylidene-imidazolinone(HBI)-type chromophores are new promising fluorescent probes,which are suitable for imaging and detection of living cells.How-ever,the lack of infrared ch...Partial genetically encoded 4-hy-droxybenzylidene-imidazolinone(HBI)-type chromophores are new promising fluorescent probes,which are suitable for imaging and detection of living cells.How-ever,the lack of infrared chro-mophores hinders the develop-ment seriously.Here more than 30 HBI-type chromophores with reg-ular structure modifications were employed and typical spectral redshift change laws and mechanisms were investigated by quantum methods.Results show that both one-photon spectrum(OPS,absorption/emission)and two-photon absorption(TPA)can achieve large redshift via either extending conjugated lengths of frag-3 or enlarging conjugated areas of frag-1 of HBI skeleton.Spectral redshifts of all chromophores are highly related to intramolecular charge transfer(ICT),but neutral ones are closely related to the total ICT or electron-accept-ing-numbers of frag-3,and the high correlative factor of anions is the aromaticity of frag-2 bridge.The frag-2 bridge with high aromaticity can open a reverse charge transfer channel in anion relative to neutral,obtaining significant redshift.Based on analysis,a new 6-hydroxyl-naphthalene-imidazolinone(HNI)series,which have larger conjugated area in frag-1,are pre-dicted.The OPS and TPA of anionic HNI ones acquire about 76−96 nm and 119−146 nm red-shift relative to traditional HBI series respectively as a whole.The longest emission of anionic HNI-4 realizes more 244 nm redshift relative to HBI-1.Our work clarifies worthy spectral reg-ularities and redshift mechanisms of HBI-type chromophores and provides valuable design strategy for infrared chromophores synthesis in experiment.展开更多
The intramolecular charge transfer dual fluorescence of p-dibutylaminobenzoic acid-b-cyclodextrin inclusion complex showed a substantially higher sensitivity toward aqueous solution pH variation when compared with tha...The intramolecular charge transfer dual fluorescence of p-dibutylaminobenzoic acid-b-cyclodextrin inclusion complex showed a substantially higher sensitivity toward aqueous solution pH variation when compared with that of p-dibutylaminobenzoic acid alone, which established a new principle for direct CT fluorescence sensing in aqueous solution by using the CT fluorophore-cyclodextrin inclusion complex.展开更多
Polydimethylsilylenes bearing pyrenyl groups exhibit emissions fromtwisted intramolecular charge transfer state between the aromatic ring and thesilicon backbone both in polar and nonpolar solvents.
In this paper the results of dynamic NMR studies on ethylmethylamino-tertiary-butyl-phenylborane (EMABPB) with or without light are reported. The NMR data were recorded on a Bruker 400 MHz NMR equipped with our custom...In this paper the results of dynamic NMR studies on ethylmethylamino-tertiary-butyl-phenylborane (EMABPB) with or without light are reported. The NMR data were recorded on a Bruker 400 MHz NMR equipped with our custom-made optical probe and with our custom-made 450 watts (W) monochromatic light sources. The molecular photochemistry including twisted intramolecular charge-transfer-excited-state (TICT) of the EMABPB in several solvents has been investigated. These results indicate that the aminoborane demonstrates multiple configurations in CD3Cl and CD2Cl2 resulting in the shifts of the signals of the alkyl groups on the nitrogen and boron. This indicates that there are some time-dependent changes at constant temperature over the irradiation interval. At ﹣60°C and the presence of light (λ = 265 nm), we observed a large change in the populations of the two sites, and this by itself indicates a modification in the rotation around the boron nitrogen bond in the excited state. By considering the existence of the TICT state, many important energy technologies may be developed with higher efficiency by controlling the back-electron transfer processes.展开更多
Time-dependent density functional theory（TDDFT） method is used to investigate the details of the excited state intramolecular proton transfer（ESIPT） process and the mechanism for temperature effect on the Enol＊/K...Time-dependent density functional theory（TDDFT） method is used to investigate the details of the excited state intramolecular proton transfer（ESIPT） process and the mechanism for temperature effect on the Enol＊/Keto＊emission ratio for the Me2N-substited flavonoid（MNF） compound. The geometric structures of the S0 and S1 states are denoted as the Enol, Enol＊, and Keto＊. In addition, the absorption and fluorescence peaks are also calculated. It is noted that the calculated large Stokes shift is in good agreement with the experimental result. Furthermore, our results confirm that the ESIPT process happens upon photoexcitation, which is distinctly monitored by the formation and disappearance of the characteristic peaks of infrared（IR） spectra involved in the proton transfer and in the potential energy curves. Besides, the calculations of highest occupied molecular orbital（HOMO） and lowest unoccupied molecular orbital（LUMO） reveal that the electronegativity change of proton acceptor due to the intramolecular charge redistribution in the S1 state induces the ESIPT. Moreover, the thermodynamic calculation for the MNF shows that the Enol＊/Keto＊emission ratio decreasing with temperature increasing arises from the barrier lowering of ESIPT.展开更多
We theoretically investigate the excited state intramolecular proton transfer(ESIPT) behavior of the novel fluorophore bis-imine derivative molecule HNP which was designed based on the intersection of 1-(hydrazonometh...We theoretically investigate the excited state intramolecular proton transfer(ESIPT) behavior of the novel fluorophore bis-imine derivative molecule HNP which was designed based on the intersection of 1-(hydrazonomethyl)-naphthalene-2-ol and 1-pyrenecarboxaldehyde. Especially, the density functional theory(DFT) and time-dependent density functional theory(TDDFT) methods for HNP monomer are introduced. Moreover, the "our own n-layered integrated molecular orbital and molecular mechanics"(ONIOM) method(TDDFT:universal force field(UFF)) is used to reveal the aggregation-induced emission(AIE) effect on the ESIPT process for HNP in crystal. Our results confirm that the ESIPT process happens upon the photoexcitation for the HNP monomer and HNP in crystal, which is distinctly monitored by the optimized geometric structures and the potential energy curves. In addition, the results of potential energy curves reveal that the ESIPT process in HNP will be promoted by the AIE effect. Furthermore, the highest occupied molecular orbital(HOMO) and lowest unoccupied molecular orbital(LUMO) for the HNP monomer and HNP in crystal have been calculated. The calculation demonstrates that the electron density decrease of proton donor caused by excitation promotes the ESIPT process. In addition, we find that the variation of atomic dipole moment corrected Hirshfeld population(ADCH) charge for proton acceptor induced by the AIE effect facilitates the ESIPT process. The results will be expected to deepen the understanding of ESIPT dynamics for luminophore under the AIE effect and provide insight into future design of high-efficient AIE compounds.展开更多
β-cyclodextrin (β-CD) induced aggregation and micelle formation of cetyltrimethylam-mnium broAnde (CTMAB) in aqueous solution is demonstrated by the dual fluorescence of p-N, N-dAnethyladrinobenzoic acid (DMABOA) ty...β-cyclodextrin (β-CD) induced aggregation and micelle formation of cetyltrimethylam-mnium broAnde (CTMAB) in aqueous solution is demonstrated by the dual fluorescence of p-N, N-dAnethyladrinobenzoic acid (DMABOA) typical of the twisted intramolecular charge transfer (TICT). The locally excited (LE) state of DMABOA is proved to have the characteristic of intramolecular charge transfer (ICT) with a polarity higher than that of ground state but lower than that of TICT state. The peak positions of the two fluorescence bands and theiI intensity ratio are employed to probe the interaction of β-CD with CTMAB. It is conc1uded that β-CD induces CTMAB aggregation as well as Ancelle formation and may change Ancelle structure. The results also indicate that TICT in aqueous solution may be affected by the anisotropy or viscosity of the medium,increasing viscosity disadvantaging the TICT process.展开更多
Graphene quantum dots(GQDs)have attracted increasing attention due to their favorable optical properties and have been widely used,e.g.,in the biomedical field.However,the properties related to the chemical structure ...Graphene quantum dots(GQDs)have attracted increasing attention due to their favorable optical properties and have been widely used,e.g.,in the biomedical field.However,the properties related to the chemical structure of GQDs,resulting in solventdependent optical properties,still remain unclear.Herein,we present the synthesis of long-wavelength emitting GQDs with a size of about 3.6 nm via a solvothermal method using oxo-functionalized graphene(oxo-G)and p-phenylenediamine as precursors and their structural and surface chemical analysis by transmission electron and atomic force microscopy(TEM;AFM)as well as Fourier-transform infrared,Raman,and X-ray photoelectron spectroscopy(FTIR;Raman;XPS).Subsequently,the influence of solvent polarity and proticity on the optical properties of the as-prepared GQDs bearing–OH,–NH_(2),–COOH and pyridine surface groups was investigated.Based on the results of the absorption and fluorescence(FL)studies,a possible luminescence mechanism is proposed.The observed solvent-induced changes in the spectral position of the FL maximum,FL quantum yield,and FL decay kinetics in protic and aprotic solvents of low and high polarity are ascribed to a combination of polarity effects,intramolecular charge transfer(ICT)processes,and hydrogen bonding.Moreover,the potential of GQDs for the optical sensing of trace amount of water was assessed.The results of our systematic spectroscopic study will promote the rational design of GQDs and shed more light on the FL mechanism of carbon-based fluorescent nanomaterials.展开更多
基金supported by the National Natural Sci-ence Foundation of China(No.U1904196,No.82073699)the Natural Science Foundation of Henan(No.222300420055).
文摘Partial genetically encoded 4-hy-droxybenzylidene-imidazolinone(HBI)-type chromophores are new promising fluorescent probes,which are suitable for imaging and detection of living cells.How-ever,the lack of infrared chro-mophores hinders the develop-ment seriously.Here more than 30 HBI-type chromophores with reg-ular structure modifications were employed and typical spectral redshift change laws and mechanisms were investigated by quantum methods.Results show that both one-photon spectrum(OPS,absorption/emission)and two-photon absorption(TPA)can achieve large redshift via either extending conjugated lengths of frag-3 or enlarging conjugated areas of frag-1 of HBI skeleton.Spectral redshifts of all chromophores are highly related to intramolecular charge transfer(ICT),but neutral ones are closely related to the total ICT or electron-accept-ing-numbers of frag-3,and the high correlative factor of anions is the aromaticity of frag-2 bridge.The frag-2 bridge with high aromaticity can open a reverse charge transfer channel in anion relative to neutral,obtaining significant redshift.Based on analysis,a new 6-hydroxyl-naphthalene-imidazolinone(HNI)series,which have larger conjugated area in frag-1,are pre-dicted.The OPS and TPA of anionic HNI ones acquire about 76−96 nm and 119−146 nm red-shift relative to traditional HBI series respectively as a whole.The longest emission of anionic HNI-4 realizes more 244 nm redshift relative to HBI-1.Our work clarifies worthy spectral reg-ularities and redshift mechanisms of HBI-type chromophores and provides valuable design strategy for infrared chromophores synthesis in experiment.
基金This work was support by NNSF of China through grants No.29975023 and No.20175020.
文摘The intramolecular charge transfer dual fluorescence of p-dibutylaminobenzoic acid-b-cyclodextrin inclusion complex showed a substantially higher sensitivity toward aqueous solution pH variation when compared with that of p-dibutylaminobenzoic acid alone, which established a new principle for direct CT fluorescence sensing in aqueous solution by using the CT fluorophore-cyclodextrin inclusion complex.
文摘Polydimethylsilylenes bearing pyrenyl groups exhibit emissions fromtwisted intramolecular charge transfer state between the aromatic ring and thesilicon backbone both in polar and nonpolar solvents.
文摘In this paper the results of dynamic NMR studies on ethylmethylamino-tertiary-butyl-phenylborane (EMABPB) with or without light are reported. The NMR data were recorded on a Bruker 400 MHz NMR equipped with our custom-made optical probe and with our custom-made 450 watts (W) monochromatic light sources. The molecular photochemistry including twisted intramolecular charge-transfer-excited-state (TICT) of the EMABPB in several solvents has been investigated. These results indicate that the aminoborane demonstrates multiple configurations in CD3Cl and CD2Cl2 resulting in the shifts of the signals of the alkyl groups on the nitrogen and boron. This indicates that there are some time-dependent changes at constant temperature over the irradiation interval. At ﹣60°C and the presence of light (λ = 265 nm), we observed a large change in the populations of the two sites, and this by itself indicates a modification in the rotation around the boron nitrogen bond in the excited state. By considering the existence of the TICT state, many important energy technologies may be developed with higher efficiency by controlling the back-electron transfer processes.
基金This work was supported by the National Natural Science Foundation of China （No.10374040, No.20703064, and No.10505001） and the Postdoctoral Science Foundation of China （No.20060390017）.
基金Project supported by the National Basic Research Program of China(Grant No.2013CB922204)the National Natural Science Foundation of China(Grant Nos.11574115 and 11704146)the Natural Science Foundation of Jilin Province,China(Grant No.20150101063JC)
文摘Time-dependent density functional theory（TDDFT） method is used to investigate the details of the excited state intramolecular proton transfer（ESIPT） process and the mechanism for temperature effect on the Enol＊/Keto＊emission ratio for the Me2N-substited flavonoid（MNF） compound. The geometric structures of the S0 and S1 states are denoted as the Enol, Enol＊, and Keto＊. In addition, the absorption and fluorescence peaks are also calculated. It is noted that the calculated large Stokes shift is in good agreement with the experimental result. Furthermore, our results confirm that the ESIPT process happens upon photoexcitation, which is distinctly monitored by the formation and disappearance of the characteristic peaks of infrared（IR） spectra involved in the proton transfer and in the potential energy curves. Besides, the calculations of highest occupied molecular orbital（HOMO） and lowest unoccupied molecular orbital（LUMO） reveal that the electronegativity change of proton acceptor due to the intramolecular charge redistribution in the S1 state induces the ESIPT. Moreover, the thermodynamic calculation for the MNF shows that the Enol＊/Keto＊emission ratio decreasing with temperature increasing arises from the barrier lowering of ESIPT.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11574115 and 11704146)
文摘We theoretically investigate the excited state intramolecular proton transfer(ESIPT) behavior of the novel fluorophore bis-imine derivative molecule HNP which was designed based on the intersection of 1-(hydrazonomethyl)-naphthalene-2-ol and 1-pyrenecarboxaldehyde. Especially, the density functional theory(DFT) and time-dependent density functional theory(TDDFT) methods for HNP monomer are introduced. Moreover, the "our own n-layered integrated molecular orbital and molecular mechanics"(ONIOM) method(TDDFT:universal force field(UFF)) is used to reveal the aggregation-induced emission(AIE) effect on the ESIPT process for HNP in crystal. Our results confirm that the ESIPT process happens upon the photoexcitation for the HNP monomer and HNP in crystal, which is distinctly monitored by the optimized geometric structures and the potential energy curves. In addition, the results of potential energy curves reveal that the ESIPT process in HNP will be promoted by the AIE effect. Furthermore, the highest occupied molecular orbital(HOMO) and lowest unoccupied molecular orbital(LUMO) for the HNP monomer and HNP in crystal have been calculated. The calculation demonstrates that the electron density decrease of proton donor caused by excitation promotes the ESIPT process. In addition, we find that the variation of atomic dipole moment corrected Hirshfeld population(ADCH) charge for proton acceptor induced by the AIE effect facilitates the ESIPT process. The results will be expected to deepen the understanding of ESIPT dynamics for luminophore under the AIE effect and provide insight into future design of high-efficient AIE compounds.
文摘β-cyclodextrin (β-CD) induced aggregation and micelle formation of cetyltrimethylam-mnium broAnde (CTMAB) in aqueous solution is demonstrated by the dual fluorescence of p-N, N-dAnethyladrinobenzoic acid (DMABOA) typical of the twisted intramolecular charge transfer (TICT). The locally excited (LE) state of DMABOA is proved to have the characteristic of intramolecular charge transfer (ICT) with a polarity higher than that of ground state but lower than that of TICT state. The peak positions of the two fluorescence bands and theiI intensity ratio are employed to probe the interaction of β-CD with CTMAB. It is conc1uded that β-CD induces CTMAB aggregation as well as Ancelle formation and may change Ancelle structure. The results also indicate that TICT in aqueous solution may be affected by the anisotropy or viscosity of the medium,increasing viscosity disadvantaging the TICT process.
基金This research is supported by the Deutsche Forschungsgemeinschaft project No.392444269(DFG,German Research Foundation),the China Scholarship Council(CSC)supported by the DFG.C.N.and A.T.acknowledge DFG financial support via the research infrastructure grant INST 275/257-1 FUGG(project No.313713174)+2 种基金funding through ESF Research Groups 2019 FGR 0080“ESTI”and 2020 FGR 0051“GraphSens”as well as BMWi project ZF4817401VS9“TDraCon”Z.H.from Soochow University is acknowledged for conducting TEM measurements.U.R.G and L.S.gratefully acknowledge financial support by the European Metrology Programme for Innovation and Research(EMPIR)as part of the projects 18HLT02“AeroTox”The EMPIR initiative is co-funded by the European Union’s Horizon 2020 research and innovation programme and by the EMPIR participating states.
文摘Graphene quantum dots(GQDs)have attracted increasing attention due to their favorable optical properties and have been widely used,e.g.,in the biomedical field.However,the properties related to the chemical structure of GQDs,resulting in solventdependent optical properties,still remain unclear.Herein,we present the synthesis of long-wavelength emitting GQDs with a size of about 3.6 nm via a solvothermal method using oxo-functionalized graphene(oxo-G)and p-phenylenediamine as precursors and their structural and surface chemical analysis by transmission electron and atomic force microscopy(TEM;AFM)as well as Fourier-transform infrared,Raman,and X-ray photoelectron spectroscopy(FTIR;Raman;XPS).Subsequently,the influence of solvent polarity and proticity on the optical properties of the as-prepared GQDs bearing–OH,–NH_(2),–COOH and pyridine surface groups was investigated.Based on the results of the absorption and fluorescence(FL)studies,a possible luminescence mechanism is proposed.The observed solvent-induced changes in the spectral position of the FL maximum,FL quantum yield,and FL decay kinetics in protic and aprotic solvents of low and high polarity are ascribed to a combination of polarity effects,intramolecular charge transfer(ICT)processes,and hydrogen bonding.Moreover,the potential of GQDs for the optical sensing of trace amount of water was assessed.The results of our systematic spectroscopic study will promote the rational design of GQDs and shed more light on the FL mechanism of carbon-based fluorescent nanomaterials.
