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| 1 | A 1,3-dipolar cycloaddition protocol to porphyrin- functionalized reduced graphene oxide with a push-pull motif显示文摘减少的 graphene 氧化物(RGO ) 是 covalently 有由二个方法的卟啉一半的 functionalized:直接 Prato 反应(即 1,3-dipolar cycloaddition ) 与 sarcosine 和包含甲酰的卟啉,并且用 4-hydroxybenzaldehyde 包含 1,3-dipolar cycloaddition 到 RGO 表面的一个逐步的方法,与适当卟啉由亲核的替换列在后面。到 RGO 表面的卟啉的化学结合被紫外 / 可见的吸收证实了,荧光, Fourier 变换红外线,并且拉曼光谱学, X 光检查粉末衍射和 X 光检查光电子光谱学,传播电子和原子力量显微镜学,和 thermogravimetric 分析;这个化学附件保证在 RGO 和卟啉之间的有效电子 / 精力转移,并且 RGO 先锋和太古的卟啉与那些相比负担得起改进光非线性。 | Aijian Wang Wang Yu Zhengguo Xiao Yinglin Song Lingliang Long Marie P. Cifuentes Mark G. Humphrey Chi Zhang | 2015 | Nano Research2015，8，3： | 7 |
| 2 | Synthesis of N-acetamide C_(60) nitride and its performance of optical limiting显示文摘N-acetamide C60 nitride (N-acetamide-1,2-dihydro-1,2-aza-fullerene[60]) has been synthesized by the reaction of C60 and azidoacetamide and initially characterized. Its mechanism was that the objective product is formed through intermediate triazoline. The computational study shows that N-nitride structure is thermodynamically more stable by using the semi-empirical AM1 SCF-MO method. The properties of optical limiting were tested by using double frequency Nd: YAG pulse laser system and showed that the optical limiting mechanism is reverse saturation absorption. At wavelength of 532 nm, compared with optical limiting for ns pulse, this new material has good optical limiting character for ps pulse. At wavelength of 707 nm. the capacity of optical limiting of the derivative is prior to C60- | TANG Guangshi, ZHU Hesun & SONG Yinglin Research Center of Materials Science, Beijing Institute of Technology, Beijing 100081, China Department of Applied Physics, Harbin Institute of Technology. Harbin 150001. China Department of Applied Chemiscy Beiji | 2000 | Chinese Science Bulletin2000，45，2： | 4 |
| 3 | Multi-walled carbon nanotubes covalently functionalized by axially coordinated metal-porphyrins: Facile syntheses and temporally dependent optical performance显示文摘向轴的方向协调了 metal-porphyrin-functionalized 多围的碳 nanotube (MWCNT ) nanohybrids 经由二条不同合成途径(一个壶 1,3-dipolar cycloaddition 反应和那深奥 1,3-dipolar cycloaddition 由亲核的替换跟随了的一条逐步的途径) 被准备,并且通过分光镜的技术描绘了。到 MWCNT 的表面的听卟啉的附件显著地改进他们处理的溶解度和容易。协调的这些向轴的方向(5,10,15,20-tetraphenylporphyrinato ) 锡(IV )(SnTPP )-MWCNTs 展览重要荧光熄灭。结果的 nanohybrids 的第三顺序的非线性的光性质被与毫微秒和微微秒激光脉搏在 532 nm 使用 Z 扫描技术学习。当分别地,毫微秒或微微秒脉搏被采用时,结果证明 nanohybrids 展出重要反向的可饱和的吸收或可饱和的吸收。在毫微秒政体的改进非线性的吸收在继续到 nanohybrids 上被观察并且被归功于到 MWCNT 和化学上依附的金属卟啉的突出的性质的联合。 | Aijian Wang Jingbao Song Zhipeng Huang Yinglin Song Wang Yu Huanli Dong Wenping Hu Marie P. Cifuentes Mark G. Humphrey Long Zhang Jianda Shao Chi Zhang | 2016 | Nano Research2016，9，2： | 3 |
| 4 | Atomically precise metal-chalcogenide semiconductor molecular nanoclusters with high dispersibility:Designed synthesis and intracluster photocarrier dynamics显示文摘A comprehensive understanding of excited-state dynamics of semiconductor quantum dots or nanomaterials at the atomic or molecular level is of scientific importance.Pure inorganic(or non-covalently protected)seimiconductor molecular nanoclusters with atomically precise structure are contributive to establish accurate correlation of excited-state dynamics with their composition/structure,however,the related studies are almost blank because of unresolved solvent dispersion issue.Herein,we designedly created the largest discrete chalcogenide seimiconductor molecular nanoclusters(denoted P2-CuMSnS,M=In or/and Ga)with great dispersibility,and revealed an interesting intracluster“core–shell”charge transfer relaxation dynamics.A systematic red shift in absorption spectra with the gradual substitution of In by Ga was experimentally and computationally investigated,and femtosecond transient absorption measurements further manifested there were three ultrafast processes in excited-state dynamics of P2 nanoclusters with the corresponding amplitudes directed by composition variation.Current results hold the great promise of the solution-processible applications of semiconductor-NC-based quantum dots and facilitate the development of atomically precise nano-chemistry. | Jiaxu Zhang Chaochao Qin Yeshuang Zhong Xiang Wang Wei Wang Dandan Hu Xiaoshuang Liu Chaozhuang Xue Rui Zhou Lei Shen Yinglin Song Dingguo Xu Zhien Lin Jun Guo Haifeng Su Dong-Sheng Li Tao Wu | 2020 | Nano Research2020，13，10： | 2 |
| 5 | The C_(6)D_(6)detector system on the Back-n beam line of CSNS显示文摘Introduction The neutron capture cross sections are very important in the field of nuclear device design and basic physics research.Hydrogen-free liquid scintillator such as C_(6)D_(6)detectors are widely used in the neutron capture cross-sectional measurements for the low neutron sensitivity and fast time response.The Back-n white neutron source at China Spallation Neutron Source is the first spallation white neutron source in China,and it is suitable for neutron capture cross-sectional measurement.Materials and methods A C_(6)D_(6)detector system was built in the Back-n experimental station.The pulse height weighting technique was used to determine the system’s detection efficiency.The response to gamma rays of the C_(6)D_(6)detector was measured,and the energy resolution function was determined.Monte Carlo simulation with Geant4 code was carried out to get the weighting function of this C_(6)D_(6)detector system.Additionally,the systematic uncertainty of the weighting function was also determined.Conclusion According to the experimental and simulation results,this C_(6)D_(6)detector system can be used to measure neutron capture cross section. | Jie Ren Xichao Ruan Jie Bao Guangyuan Luan Wei Jiang Qi An Huaiyong Bai Ping Cao Qiping Chen Yonghao Chen Pinjing Cheng Zengqi Cui Ruirui Fan Changqing Feng Minhao Gu Fengqin Guo Changcai Han Zijie Han Guozhu He Yongcheng He Yuefeng He Hanxiong Huang Weiling Huang Xiru Huang Xiaolu Ji Xuyang Ji Haoyu Jiang Hantao Jing Ling Kang Mingtao Kang Bo Li Lun Li Qiang Li Xiao Li Yang Li Yang Li Rong Liu Shubin Liu Xingyan Liu Yinglin Ma Changjun Ning Binbin Qi Zhaohui Song Hong Sun Xiaoyang Sun Zhijia Sun Zhixin Tan Hongqing Tang Jingyu Tang Pengcheng Wang Qi Wang Taofeng Wang Yanfeng Wang Zhaohui Wang Zheng Wang Jie Wen Zhongwei Wen Qingbiao Wu Xiaoguang Wu Xuan Wu Likun Xie Yiwei Yang Han Yi Li Yu Tao Yu Yongji Yu Guohui Zhang Jing Zhang Linhao Zhang Liying Zhang Qingmin Zhang Qiwei Zhang Xianpeng Zhang Yuliang Zhang Zhiyong Zhang Yingtan Zhao Liang Zhou Zuying Zhou Danyang Zhu Kejun Zhu Peng Zhu | 2019 | Radiation Detection Technology and Methods2019，3，3： | 1 |
| 6 | Reflection 4F coherent imaging technique for measurements of optical nonlinearity显示文摘 | Yang Junyi Song Yinglin Wang Yuxiao | | 0，，： | 1 |
| 7 | Effect of Aspect Ratio on Field Emission Properties of ZnO Nanorod Arrays显示文摘 | Xuemin Qian Huibiao Liu Yanbing Guo Yinglin Song Yuliang Li | 2008 | Nanoscale Research Letters2008，，8： | 1 |
| 8 | Crystal structures and third - order NLO properties in DMF solution of Co(Ⅱ) - bpfp coordination polymers ( bpfp= N, N' bis (pyridylformyl) piperazine 显示文摘 | HONG XU YINGLIN SONG HONGWEI HOU | 2004 | Inorganica Chimica Acta2004，357，12： | 1 |
| 9 | Optical nonlinearity and optical limiting properties of new metal cluster 显示文摘 | YINGLIN SONG CHI ZHANG YUXIAO WANG | 1999 | Optics Communications1999，168，2： | 1 |
| 10 | Synthesis, Crystal Structures, and Third -Order Nonli- near Optical Properties of a Series of Ferrocenyl Organometallics显示文摘 | Gang Li Yinglin Song | 2003 | Inorganic chemistry2003，42，3： | 1 |
| 11 | Self-assembly of interpenetrating coordination nets formed from interpenetrating cationic and anionic three-dimensional diamondoid cluster coordination polymers显示文摘 | Liang Kai Zheng Hegen Song Yinglin | 2004 | Angew Chem Int Ed2004，43，： | 1 |
| 12 | Direct observation of the transient thermal-lensing effect using the phase-object Z- scan technique显示文摘 | Yang Junyi Song Yinglin | 2009 | Optics Letters2009，34，： | 1 |
| 13 | Time- resolved pump-probe technology with phase object for measurements of optical nonlinearities 显示文摘 | Yang Junyi Song Yinglin Wang Yuxiao | 2009 | Opt Exp2009，17，： | 1 |
| 14 | Third-order nonlinear optical properties of Bi2S3 and Sb2S3 nanorods studied by the Z-scan technique显示文摘 | Cun Li Guang Shi Yinglin Song | 2008 | Journal of Physics and Chemistry of Solids2008，69，7： | 1 |
| 15 | 显示文摘 | Chen Xingbo Shi Guang Song Yinglin | 2008 | Dyes and Pigments2008，77，： | 1 |
| 16 | Localization and threshold of bistable switching by gap-edge shifting显示文摘 | Chen Lixue Kim Dalwoo Song Yinglin | | 0，，09： | 1 |
| 17 | 5-HMF attenuates inflammation and demyelination in experimental autoimmune encephalomyelitis mice by inhibiting the MIF-CD74 interaction显示文摘The neuroprotective role of 5-hydroxymethyl-2-furfural(5-HMF)has been demonstrated in a variety of neurological diseases.The aim of this study is to investigate the effect of 5-HMF on multiple sclerosis(MS).IFN-γ-stimulated murine microglia(BV2 cells)are considered a cell model of MS.With 5-HMF treatment,microglial M1/2 polarization and cytokine levels are detected.The interaction of 5-HMF with migration inhibitory factor(MIF)is predicted using online databases.The experimental autoimmune encephalomyelitis(EAE)mouse model is established,followed by a 5-HMF injection.The results show that 5-HMF facilitates IFN-γ-stimulated microglial M2 polarization and attenuates the inflammatory response.According to the network pharmacology and molecular docking results,5-HMF has a binding site for MIF.Further results show that blocking MIF activity or silencing CD74 enhances microglial M2 polarization,reduces inflammatory activity,and prevents ERK1/2 phosphorylation.5-HMF inhibits the MIF-CD74 interaction by binding to MIF,thereby inhibiting microglial M1 polarization and enhancing the anti-inflammatory response.5-HMF ameliorates EAE,inflammation,and demyelination in vivo.In conclusion,our research indicates that 5-HMF promotes microglial M2 polarization by inhibiting the MIF-CD74 interaction,thereby attenuating inflammation and demyelination in EAE mice. | Dongsheng Guan Yingxia Li Yinglin Cui Huanghong Zhao Ning Dong Kun Wang Deqi Ren Tiantian Song Xiaojing Wang Shijie Jin Yinghe Gao Mengmeng Wang | 2023 | Acta Biochimica et Biophysica Sinica2023，55，8： | 0 |
| 18 | Root Multiplicity of a Special Generalized Kac- Moody Algebra EB2显示文摘 | Xinfang Song Yinglin Guo | 2014 | 数学计算(中英文版)2014，3，3： | 0 |
| 19 | Enabling ultranarrow blue emission linewidths in colloidal alloy quantum dots by decreasing the exciton fine structure splitting and exciton–phonon coupling显示文摘The realization of colloidal alloy quantum dots(QDs)with narrow spectral linewidths requires minimization of the contributions of inhomogeneous and homogeneous broadening to the ensemble spectrum.Recently,there has been remarkable progress in eliminating the inhomogeneous contribution by controlling the size distribution of the QDs.However,considerable challenges remain in suppressing the homogeneous broadening,in terms of both intrinsic principles and rational synthetic routes.We find that ground-state exciton fine structure splitting and exciton-phonon coupling play a pivotal role in the homogeneous broadening mechanism.Here we demonstrate that the elimination of the lattice mismatch strain by using a coherent strain structure can decrease the light-heavy hole splitting,thus suppressing the asymmetric broadening of the emission on the high energy side.Besides,the improvement of the uniformity of the alloy by using a stepwise ion exchange strategy can weaken the exciton-longitudinal optical(LO)-phonon interactions,further minimizing the homogeneous broadening.As a result,the final alloy QD products exhibit a widely tunable blue emission wavelength(445-470 nm)with the narrowest ensemble photoluminescence full width at half maximum(FWHM)of 10.1-13.5 nm(or 58.4-75.3 meV).Our study provides a potential strategy for other semiconductor nanocrystals with ultranarrow spectral linewidths. | Jinke Bai Linfeng Wang Tingting Zhang Tianyi Hou Meilun Zhang Bing Xu Dongyu Li Xiao Jin Qinghua Li Yuxiao Wang Xueru Zhang Yinglin Song | 2023 | Nano Research2023，16，1： | 0 |
| 20 | Butterfly and Nest-Shaped Tp*-W-Cu-S Cluster Monomers and Dimers with Hexamethylenetetramine as Ligand:Anion-Dependent Structures and Nonlinear Optical Properties显示文摘Main observation and conclusion The assembly of[Et4N][Tp*WS3](1)with CuX(Tp*=hydridotris(3,5-dimethylpyrazol-1-yl)borate;X=Cl,Br,andI)or[Cu(MeCN)][PF6]in the presence of tetratopic ligand hexamethylenetetramine(HMT)afforded an array of four cluster-based compounds,which are either neutral or anionic.These compounds include[Tp*WSzCu3Cl2(HMT)](2,monomer,neutral),[Tp*WSzCugBr2(HMT)](3,monomer,neutral),[Tp*WSzCu3l1 s(HMT)21(4,dimer,anionic),and[Tp*WSzCu2(HMT)]2(PFc)2(5,dimer,anionic).The size of the halogen is found to dictate the structures(2/3 versus 4),and the presence/absence of halogen also affects the utiliation of coordinate site of HMT(4 versus 5)by creating more available CuOite in the case of 5.The structures of 2-5 are also characterized using elemental analysis,Fourier-transform infrared(FT-IR)spectra,and ultraviolet-visible(UV-Vis)spectroscopy,with the dimeric structure of 5 also selected for the third-order nonlinear optical(NLO)property investigations.The NLO measurement results suggest that the hyperpola rizability value(v)of 5,reflecting its NLO properties as a neat material,features 2.12×10^(-30)esu,and it is comparable to other W/Cu/S clus-terbased molecular entities,rendering 5 a promising NLO-active material. | Quan Liu Mingie Lu Lice Yu Yinglin Song Jianping Lang | 2021 | Chinese Journal of Chemistry2021，39，3： | 0 |
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