The title compound (C20H30N4O6, Mr = 422.48) was synthesized and its crystal structure was determined by X-ray diffraction method. It crystallizes in the triclinic system, space group P with cell parameters: a = 8.330...The title compound (C20H30N4O6, Mr = 422.48) was synthesized and its crystal structure was determined by X-ray diffraction method. It crystallizes in the triclinic system, space group P with cell parameters: a = 8.330(2), b = 8.468(2), c = 16.017(3) ? ?= 97.30(3), ?= 92.33(3), ?= 103.94(3)? V = 1084.7(4) ?, Dc = 1.294 g/cm3, Z = 2, F(000) = 452 and ?= 0.096 mm-1. The structure was refined to R = 0.0483 for 3732 observed reflections with I > 2s(I) and wR = 0.1335 for 4828 unique reflections. The hydantoin rings are planar and the two ring planes of one molecule are paralleled to each other.展开更多
As indicated by kinetic ESR measurements, the key factor to affect electron recombination in the process of PET between C60 and amines is the space between donor and C60. To increase solubility of C60 in water, it was...As indicated by kinetic ESR measurements, the key factor to affect electron recombination in the process of PET between C60 and amines is the space between donor and C60. To increase solubility of C60 in water, it was incorporated into micelle of surfactants. ]展开更多
Mesoporous molecular sieves possessing high mesopore volumes and large specific surface areas were prepared and characterized by means of XRD, low temperature N_2 adsorption-desorption measurements, FT IR, Raman, UV...Mesoporous molecular sieves possessing high mesopore volumes and large specific surface areas were prepared and characterized by means of XRD, low temperature N_2 adsorption-desorption measurements, FT IR, Raman, UV-visible diffuse reflectance and XPS spectroscopy. The materials contain both framework and extra-framework Ti centers which exhibit selective oxidation catalytic activity and photocatalytic activity respectively. The catalysis of selective oxidation was studied with the hydroxylation of benzene with hydrogen peroxide and photochemical activity was studied by the yields of ·OH and H_2O_2, respectively.展开更多
UV-Vis, fluorescence spectroscopy and time resolved spectroscopic technique on picosecond and femto- second scales have been utilized to investigate the effect of steric hindrance and multiple hydroxyl groups of solve...UV-Vis, fluorescence spectroscopy and time resolved spectroscopic technique on picosecond and femto- second scales have been utilized to investigate the effect of steric hindrance and multiple hydroxyl groups of solvents on the barrierless isomerization in excited state of 3, 3′- di(3-sulfopropyl)thiacyanine triethylaminium salt. The re-sults show that the factors mentioned above may be respon-sible for a different 搒hort-time behavior?of the bleaching signal on the ground state and nonlinear viscosity depend-ence of the excited-state lifetime in isopropanol and glycol. These phenomena are distinguished from the situation re-ported in the long-chained monohydroxyl alcohol solvents. However, the dye molecule still exhibits the analyzing- wavelength dependence of the observed fluorescence lifetime, that is, the fluorescence lifetime increases with the increasing of analyzing-wavelength. The conclusions are in agreement with those drawn from femtosecond upconversion fluores-cence experiments and further exemplify the barrierless isomerization model in the excited state.展开更多
Nanosecond laser pulse photolysis was used to investigate the excited-state dynamics of the photonuclease vitamin-K3 (VK3). A spectral band peaked at 285 nm was newly observed and attributed to the triplet-excited sta...Nanosecond laser pulse photolysis was used to investigate the excited-state dynamics of the photonuclease vitamin-K3 (VK3). A spectral band peaked at 285 nm was newly observed and attributed to the triplet-excited state of VK3. In studying the photochemistry between the photonu-clease VK3 and guanine nucleotide (dGMP), we obtained spectroscopic evidence for the photo-initiated formation of both VK3 radical anion and dGMP radical cation, and thus proved the charge transfer reaction between the trip-let-excited VK3 and the ground-state dGMP.展开更多
基金This project was supported by the National Natural Science Foundation of China (No 39870983)
文摘The title compound (C20H30N4O6, Mr = 422.48) was synthesized and its crystal structure was determined by X-ray diffraction method. It crystallizes in the triclinic system, space group P with cell parameters: a = 8.330(2), b = 8.468(2), c = 16.017(3) ? ?= 97.30(3), ?= 92.33(3), ?= 103.94(3)? V = 1084.7(4) ?, Dc = 1.294 g/cm3, Z = 2, F(000) = 452 and ?= 0.096 mm-1. The structure was refined to R = 0.0483 for 3732 observed reflections with I > 2s(I) and wR = 0.1335 for 4828 unique reflections. The hydantoin rings are planar and the two ring planes of one molecule are paralleled to each other.
文摘As indicated by kinetic ESR measurements, the key factor to affect electron recombination in the process of PET between C60 and amines is the space between donor and C60. To increase solubility of C60 in water, it was incorporated into micelle of surfactants. ]
基金Supported by the State Major Basic Research Project of China(No. 2 0 0 0 0 4 80 0 9) and the National Natural ScienceFoundation of China(No. 2 0 1730 0 3)
文摘Mesoporous molecular sieves possessing high mesopore volumes and large specific surface areas were prepared and characterized by means of XRD, low temperature N_2 adsorption-desorption measurements, FT IR, Raman, UV-visible diffuse reflectance and XPS spectroscopy. The materials contain both framework and extra-framework Ti centers which exhibit selective oxidation catalytic activity and photocatalytic activity respectively. The catalysis of selective oxidation was studied with the hydroxylation of benzene with hydrogen peroxide and photochemical activity was studied by the yields of ·OH and H_2O_2, respectively.
基金supported by the State Key Basis Research and Development Plans(Grant No.G1998010100)the National Natural Science Foundation of China(Grant Nos.3989039 and 90101010).
文摘UV-Vis, fluorescence spectroscopy and time resolved spectroscopic technique on picosecond and femto- second scales have been utilized to investigate the effect of steric hindrance and multiple hydroxyl groups of solvents on the barrierless isomerization in excited state of 3, 3′- di(3-sulfopropyl)thiacyanine triethylaminium salt. The re-sults show that the factors mentioned above may be respon-sible for a different 搒hort-time behavior?of the bleaching signal on the ground state and nonlinear viscosity depend-ence of the excited-state lifetime in isopropanol and glycol. These phenomena are distinguished from the situation re-ported in the long-chained monohydroxyl alcohol solvents. However, the dye molecule still exhibits the analyzing- wavelength dependence of the observed fluorescence lifetime, that is, the fluorescence lifetime increases with the increasing of analyzing-wavelength. The conclusions are in agreement with those drawn from femtosecond upconversion fluores-cence experiments and further exemplify the barrierless isomerization model in the excited state.
文摘Nanosecond laser pulse photolysis was used to investigate the excited-state dynamics of the photonuclease vitamin-K3 (VK3). A spectral band peaked at 285 nm was newly observed and attributed to the triplet-excited state of VK3. In studying the photochemistry between the photonu-clease VK3 and guanine nucleotide (dGMP), we obtained spectroscopic evidence for the photo-initiated formation of both VK3 radical anion and dGMP radical cation, and thus proved the charge transfer reaction between the trip-let-excited VK3 and the ground-state dGMP.
