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Theoretical study of the electronic structures and spectroscopic properties of [(4'-XC≡Ctrpy)PtCl]^+ (trpy=2,2':6',2"-terpyridine;X=H,Me and Ph)

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Science china chemistry 2009年第12期52卷 2226-2236页

作者： WANG xin,BAI FuQuan,zhou xin,LIU Tao & {3. hongxing state key laboratory of Theoretical and computational chemistry,institute of Theoretical chemistry,jilin {13.,changchun 13.023.china 1. state key laboratory of Theoretical and {3. chemistry Institute of Theoretical Chemistry Jilin University Changchun 130023 China

The electronic structures and spectroscopic properties of [(4'-XC≡Ctrpy)PtCl]+(trpy = 2,2':6',2″-terpyridine; X = H (1),methyl (Me) (2),and phenyl (Ph) (3. were studied by the ab initio method. The structures at the ground and excited state were optimized at the B3.YP and CIS levels,respectively. The absorption and emission spectra in the dichloromethane solution were obtained by using the TD-DFT (B3.YP) method associated with the PCM model. The molecular orbital energy of the HOMOs of 1-3.with the d(Pt),p(Cl),π(trpy),and π(XC≡C) character is sensitive to the substituents on the acetylide ligand,but that of the trpy-based LUMOs with the π*(trpy) character varies slightly. The lowest lying emission at 503.nm for 1 is mainly attributed to the 3.LCT perturbed by the 3.LCT and 3.LCT transitions,but that at 53. nm for 2,and that at 558 nm for 3.are mainly attributed to the 3.LCT perturbed by the 3.LCT and 3.LCT transitions. The different electron-donating ability of H,Me,and Ph is responsible for the differences in emission character. Moreover,the calculation results show that the phosphorescent color can be turned by adjusting the substituents. Both the lowest energy absorption and emission of 1―3.are red-shifted in the order of 13.consistent with the electron-donating of H

关键词： platinum(Ⅱ) complexes TD-DFT absorption spectra charge transfer luminescence

Theoretical studies on Ru(fppz)_2(CO)L (L=N-heterocyclic ligand):Electronic structure,absorption,phosphorescence,and solvatochromism

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Science china chemistry 2008年第12期51卷 1211-1220页

作者： LIU Tao1, zhou xin1, BAI FuQuan1, zhang JianPo1, XIA BaoHui1,2, PAN QingJiang3.& zhang hongxing1 1 state key laboratory of Theoretical and computational chemistry, institute of Theoretical chemistry, jilin university,{13. 2 College of chemistry, jilin university,{13. 3.laboratory of Physical chemistry, School of chemistry and Materials Science, Heilongjiang university, Harbin 150080, china state key laboratory of Theoretical and {3. chemistry Institute of Theoretical Chemistry Jilin University Changchun 130023 China College of chemistry Jilin University Changchun 130023 China laboratory of Physical chemistry School of Chemistry and Materials Science Heilongjiang University Harbin 150080 China

A series of ruthenium(II) complexes Ru(fppz)2(CO)L [fppz = 3.trifluoromethyl-5(2-pyridyl)pyrazole; L = pyridine (1), 4-dimethylaminopyridine (2), 4-cyanopyridine (3.] were designed and investigated theo-retically to explore their electronic structures, absorption, and emissions as well as the solvatochrom-ism. The singlet ground state and triplet excited state geometries were fully optimized at the B3.YP/LANL2DZ and CIS/LANL2DZ level, respectively. The HOMO of 1-3.is composed of dyz(Ru) atom and π(fppz). The LUMO of 1 and 2 is dominantly contributed by π*(fppz) orbital, but that of 3.is con-tributed by π*(L). Absorption and phosphorescence in vacuo, C6H12, and CH3.N media were calculated using the TD-DFT level of theory with the PCM model based on the optimized ground and excited state geometries, respectively. The lowest-lying absorption of 1 and 2 at 3.7 and 3.1 nm is attributed to {[dyz(Ru) + π(fppz)] → [π*(fppz)]} transition, but that of 3.at 479 nm is assigned to {[dyz(Ru) + π(fppz)] → [π*(L)]} transition. The phosphorescence of 1 and 2 at 43. and 43. nm originates from 3.[dyz(Ru) + π(fppz)] [π*(fppz)]} excited state, while that of 3.at 606 nm is from 3.[dyz(Ru) + π(fppz)] [π*(L)]} excited state. The calculation results showed that the absorption and emission transition character can be changed from MLCT/ILCT to MLCT/LLCT transition by altering the substituent on the L ligand. The phosphorescence of 1 and 2 does not have solvatochromism, but that of 3.at 606 nm (vacuo), 584 nm (C6H12), and 541 nm (CH3.N) is strongly dependent on the solvent polarity, so introducing elec-tron-withdrawing group on ligand L will induce remarkable solvatochromism.

关键词： ruthenium complex DFT phosphorescence solvatochromism

DFT and TDDFT investigations on the ground and excited states for polynuclear platinum(II) complexes containing the rigid phenylacetylide ligand

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Science china chemistry 2007年第5期50卷 599-606页

作者： zhou xin1, PAN QingJiang2, LI MingXia1,2, zhang {3.1 & Tang AuChin1 1 state key laboratory of Theoretical and computational chemistry, institute of Theoretical chemistry, jilin university, changchun 13.023. china 2 School of chemistry and Materials Science, Heilongjiang university, Harbin 150080, china state key laboratory of Theoretical and {3. chemistry Institute ofTheoretical ChemistryJilin UniversityChangchun 130023China School of chemistry and MaterialsScience Heilongjiang UniversityHarbin 150080China

We have studied the ground and excited states of the three dendriticpolynuclear Pt(ll) complexes 1-[Cl(PH3.2PtC ident to C]-3.5-[HC ident to C]C6H3.(1),1,3.[CI(PH3.2PtCident to C]2-5-[HC ident to C]C6H3.(2),and 1,3.5-[CI(PH3.2-PtC ident to C]3.6H3.(3.,by using theB3.YP and UB3.YP methods,*** approach with the PCM model was performed to predict theemission spectra properties of 1-3.in CH2Cl2 *** first predicted the excited-stategeometries for the three *** the change of the number of Pt(ll) atom,1-3.show thedifferent geometry structures in both the ground and excited states;furthermore,the increase of themetal density from 1 to 3.results in the red shift of the lowest-energy emissions along *** luminescent properties of 1 are somewhat different from those of 2 and *** emissionproperties of 2 and 3.are richer than *** conclusion can give a good support for designing thehigh efficient luminescent materials.

关键词： excited state luminescence dendritic platinum(ll) complexes DFT TDDFT

The first principle study on the spectra of FPt monomer and its excimer

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Science china chemistry 2011年第6期54卷 968-974页

作者： zhou xin zhang {3. PAN QingJiang institute of Theoretical and Simulation chemistry Academy of Fundamental and Interdisciplinary Science Harbin Institute of Technology Harbin 150008 China state key laboratory of Theoretical and {3. chemistry Institute of Theoretical Chemistry Jilin University Changchun 130023 China School of chemistry and Materials Science Heilongjiang University Harbin 150080 China

The structural, electronic and spectroscopic properties of monomer FPt (2-(4′,6′-difluorophenyl)pyridinato-N,C2′)(2,4-pentanedionato-O,O) (1) and dimer [FPt]2 (2) were explored within the density functional theory (DFT) and time-dependent DFT (TD-DFT). The calculated geometry parameters and spectroscopic results agree well with the experimental observation. In the ground state, FPt exists in the form of monomer, while in the excited state, dimer [FPt]2 forms with a Pt-Pt contraction of 0.05 nm due to the promotion of σ[dz2(Pt2)] to π*(phenylryridyl) and σ[pz(Pt2)]. Transition properties of monomer and excimer are different in nature: the former originates from mixed transitions of 3.LCT and 3.LCT, while the latter is dominated by 3.MLCT transition.

关键词： WOLDE luminescent properties excited state

系列二亚胺Os(Ⅱ)配合物[Os(L)_2(CN)_2(phen)](L=PH_3.DMSO;phen=1,10-邻二氮杂菲)及[Os(PH_3._2(phen)Br_2]电子结构和光谱性质的理论研究

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化学学报 2009年第3期67卷 197-202页

作者：吴玉辉周欣张红星吉林大学理论化学研究所理论化学计算国家重点实验室长春130023

采用自旋限制和非限制B3.YP/UB3.YP方法分别优化了系列Os(Ⅱ)二亚胺配合物[Os(L)2(CN)2(phen)][phen=1,10-邻二氮杂菲;L=PH3.1),二甲基亚砜(DMSO)(2)]及[Os(PH3.2(phen)Br2](3.的基态和激发态几何构型.通过TD-DFT方法结合PCM溶剂化模型计算了配合物1～3.二氯甲烷溶液中的吸收和发射光谱并指认了相应的跃迁性质.通过理论化学计算,揭示了π酸配体及π碱配体对配合物磷光发射性质的影响及原因.并进一步解释了配合物3.于在Os—Br键处断裂而发生反应的量子化学机理.对配合物在不同溶剂中的磷光发射性质的计算表明,溶剂对配合物的量子产率存在着影响并且配合物具有溶剂化显色效应。

关键词： Os(Ⅱ)配合物激发态密度泛函理论 TD—DFT 溶剂化效应

CEPC Technical Design Report

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Radiation Detection Technology and Methods 2024年第1期8卷 I0003-I0016,1-1091页

作者： Waleed Abdallah Tiago Carlos Adorno de Freitas Konstantin Afanaciev Shakeel Ahmad Ijaz Ahmed Xiaocong Ai Abid Aleem Wolfgang Altmannshofer Fabio Alves Weiming An Rui An Daniele Paolo Anderle Stefan Antusch Yasuo Arai Andrej Arbuzov Abdesslam Arhrib Mustafa Ashry Sha Bai Yu Bai Yang Bai Vipul Bairathi Csaba Balazs Philip Bambade Yong Ban Tripamo Bandyopadhyay Shou-Shan Bao Desmond P.Barber Ayse Bat Varvara Batozskaya Subash Chandra Behera Alexander Belyaev Michele Bertucci Xiao-Jun Bi Yuanjie Bi Tianjian Bian Fabrizio Bianchi Thomas Biekotter Michela Biglietti Shalva Bilanishvili Deng Binglin Denis Bodrov Anton Bogomyagkov Serge Bondarenko Stewart Boogert Maarten Boonekamp Marcello Borri Angelo Bosotti Vincent Boudry Mohammed Boukidi Igor Boyko Ivanka Bozovic Giuseppe Bozzi Jean-Claude Brient Anastasiia Budzinskaya Masroor Bukhari Vladimir Bytev Giacomo Cacciapaglia Hua Cai Wenyong Cai wujun Cai Yijian Cai Yizhou Cai Yuchen Cai Haiying Cai Huacheng Cai Lorenzo Calibbi Junsong Cang Guofu Cao Jianshe Cao Antoine Chance Xuejun Chang Yue Chang Zhe Chang xinyuan Chang Wei Chao Auttakit Chatrabhuti Yimin Che Yuzhi Che Bin Chen Danping Chen Fuqing Chen Fusan Chen Gang Chen Guoming Chen Hua-xing Chen Huirun Chen Jinhui Chen Ji-Yuan Chen Kai Chen Mali Chen Mingjun Chen Mingshui Chen Ning Chen Shanhong Chen Shanzhen Chen Shao-Long Chen Shaomin Chen Shiqiang Chen Tianlu Chen Wei Chen Xiang Chen Xiaoyu Chen xin Chen Xun Chen Xurong Chen Ye Chen Ying Chen Yukai Chen Zelin Chen Zilin Chen Gang Chen Boping Chen Chunhui Chen Hok Chuen Cheng Huajie Cheng Shan Cheng Tongguang Cheng Yunlong Chi Pietro Chimenti Wen Han Chiu Guk Cho Ming-Chung Chu Xiaotong Chu Ziliang Chu Guglielmo Coloretti Andreas Crivellin Hanhua Cui Xiaohao Cui Zhaoyuan Cui Brunella D'Anzi Ling-Yun Dai xinchen Dai Xuwen Dai Antonio De Maria Nicola De Filippis Christophe De La Taille Francesca De Mori Chiara De Sio Elisa Del Core Shuangxue Deng Wei-Tian Deng Zhi Deng Ziyan Deng Bhupal Dev Tang Dewen Biagio Di Micco Ran Ding Siqin Dingl Yadong Ding Haiyi Dong Jianin AGH university of Science and Technology Faculty of Physics and Applied Computer ScienceKrakow Anhui university HefeiAnhui Applied Physics Department Federal Urdu University of ArtsScience and TechnologyIslamabad Banaras Hindu university Institute of ScienceVaranasi Bandirma Onyedi Eylul university Bandirma Beihang university Beijing Beijing computational Science Research Center Beijing Beijing Conveyi LTD Beijing Beijing Glass Research institute Co. LtdBeijing Beijing institute of Technology Beijing Beijing Normal university Beijing Brown university ProvidenceRI Budker institute of Nuclear Physics Novosibirsk Cadi Ayyad university Laboratory of Fundamental and Applied PhysicsPolydisciplinary FacultyMarrakech Cairo university Giza Center for Theory and Computation National Tsing Hua UniversityHsinchu Central china Normal university WuhanHubei Central South university ChangshaHunan Centro de Fisica Teorica de Particulas Universidade Tecnica de LisboaLisboa Chengdu KaitengSifang Digital Radio&TV Equipment Co. LtdChengduSichuan china academy of engineering physics MianyangSichuan china building materials academy Beijing china Center of Advanced Science and Technology Beijing china institute of Atomic Energy Beijing china Jiliang university HangzhouZhejiang china Nuclear Instrument CO. LTDBeijing china university of Geosciences Beijing china university of Geosciences WuhanHubei china university of Mining and Technology XuzhouJiangsu china West Normal university NanchongSichuan Chongqing university Department of PhysicsChongqing Chulalongkorn university Bangkok City university of Hong Kong Department of PhysicsHong Kong Cockcroft institute Daresbury Cornell university IthacaNY CPPM(AMU/IPhU&CNRS/INP) Marseille Dalian Minzu university DalianLiaoning Dalian university of Technology Department of PhysicsDalian Deutsches Elektronen-Synchrotron DESY Hamburg Dzhelepov laboratory of Nuclear Problems of Joint institute for Nuclear Research(DLNP JINR) Dubna East china university Of Science And Technol

The Circular Electron Positron Collider(CEPC)is a large scientific project initiated and hosted by china,fostered through extensive collaboration with international *** complex comprises four accelerators:a 3. GeV Linac,a 1.1 GeV Damping Ring,a Booster capable of achieving energies up to 180 GeV,and a Collider operating at varying energy modes(Z,W,H,and tt).The Linac and Damping Ring are situated on the surface,while the subterranean Booster and Collider are housed in a 100 km circumference underground tunnel,strategically accommodating future expansion with provisions for a potential Super Proton Proton Collider(SPPC).The CEPC primarily serves as a Higgs *** its baseline design with synchrotron radiation(SR)power of 3. MW per beam,it can achieve a luminosity of 5×10^(3.)cm^(-2)s^(-1)per interaction point(IP),resulting in an integrated luminosity of 13.ab^(-1)for two IPs over a decade,producing 2.6 million Higgs *** the SR power to 50 MW per beam expands the CEPC's capability to generate 4.3.million Higgs bosons,facilitating precise measurements of Higgs coupling at sub-percent levels,exceeding the precision expected from the HL-LHC by an order of *** Technical Design Report(TDR)follows the Preliminary Conceptual Design Report(Pre-CDR,2015)and the Conceptual Design Report(CDR,2018),comprehensively detailing the machine's layout,performance metrics,physical design and analysis,technical systems design,R&D and prototyping efforts,and associated civil engineering ***,it includes a cost estimate and a preliminary construction timeline,establishing a framework for forthcoming engineering design phase and site selection *** is anticipated to begin around 2027-2028,pending government approval,with an estimated duration of 8 *** commencement of experiments and data collection could potentially be initiated in the mid-203.s.

关键词： initiated exceeding precise