A Joint Photoelectron Spectroscopy and Theoretical Study on the Electronic Structure of UCl5−and UCl5
出版年份 2013 全文链接
标题
A Joint Photoelectron Spectroscopy and Theoretical Study on the Electronic Structure of UCl5−and UCl5
作者
关键词
-
出版物
Chemistry-An Asian Journal
Volume 8, Issue 10, Pages 2489-2496
出版商
Wiley
发表日期
2013-07-13
DOI
10.1002/asia.201300627
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Probing the Electronic Structure and Chemical Bonding in Tricoordinate Uranyl Complexes UO2X3– (X = F, Cl, Br, I): Competition between Coulomb Repulsion and U–X Bonding
- (2013) Jing Su et al. INORGANIC CHEMISTRY
- Redox Equilibria of the U4+/U3+ and U3+/U Couples in Molten LiCl-RbCl Eutectic
- (2012) Takayuki NAGAI et al. ELECTROCHEMISTRY
- Photoelectron spectroscopy and the electronic structure of the uranyl tetrachloride dianion: UO2Cl42−
- (2012) Phuong Diem Dau et al. JOURNAL OF CHEMICAL PHYSICS
- Note: Photoelectron spectroscopy of cold UF5−
- (2012) Phuong Diem Dau et al. JOURNAL OF CHEMICAL PHYSICS
- Photoelectron spectroscopy and theoretical studies of UF5− and UF6−
- (2012) Phuong Diem Dau et al. JOURNAL OF CHEMICAL PHYSICS
- Determining Relative f and d Orbital Contributions to M–Cl Covalency in MCl62– (M = Ti, Zr, Hf, U) and UOCl5– Using Cl K-Edge X-ray Absorption Spectroscopy and Time-Dependent Density Functional Theory
- (2012) Stefan G. Minasian et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- The electronic structure and chemical bonding in gold dihydride: AuH2− and AuH2
- (2012) Hong-Tao Liu et al. Chemical Science
- Observation and investigation of the uranyl tetrafluoride dianion (UO2F42−) and its solvation complexes with water and acetonitrile
- (2012) Phuong Diem Dau et al. Chemical Science
- Theoretical Study of the Luminescent States and Electronic Spectra of UO2Cl2in an Argon Matrix
- (2011) Jing Su et al. Journal of Chemical Theory and Computation
- Electronic Structure of U (III) and U (IV) Ions in a LiCl–KCl eutectic melt at 450°C
- (2011) Young-Hwan Cho et al. MICROCHEMICAL JOURNAL
- Probing the electronic structure and chemical bonding of the “staple” motifs of thiolate gold nanoparticles: Au(SCH3)2− and Au2(SCH3)3−
- (2011) Chuan-Gang Ning et al. PHYSICAL CHEMISTRY CHEMICAL PHYSICS
- The mixed cyanide halide Au(i) complexes, [XAuCN]− (X = F, Cl, Br, and I): evolution from ionic to covalent bonding
- (2011) Hong-Tao Liu et al. Chemical Science
- NWChem: A comprehensive and scalable open-source solution for large scale molecular simulations
- (2010) M. Valiev et al. COMPUTER PHYSICS COMMUNICATIONS
- Photoelectron Imaging and Spectroscopy of MI2−(M = Cs, Cu, Au): Evolution from Ionic to Covalent Bonding†
- (2010) Yi-Lei Wang et al. JOURNAL OF PHYSICAL CHEMISTRY A
- Electronic absorption spectra of U (III) ion in a LiCl–KCl eutectic melt at 450°C
- (2010) Young Hwan Cho et al. MICROCHEMICAL JOURNAL
- Theoretical Actinide Molecular Science
- (2009) Georg Schreckenbach et al. ACCOUNTS OF CHEMICAL RESEARCH
- Vibrationally Resolved Photoelectron Spectroscopy of Di-Gold Carbonyl Clusters Au2(CO)n−(n= 1−3): Experiment and Theory†
- (2009) Yi-Lei Wang et al. JOURNAL OF PHYSICAL CHEMISTRY A
- Evidence of Significant Covalent Bonding in Au(CN)2−
- (2009) Xue-Bin Wang et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Photoelectron Spectroscopy of Multiply Charged Anions
- (2008) Xue-Bin Wang et al. Annual Review of Physical Chemistry
- In Situ Spectroscopy and Spectroelectrochemistry of Uranium in High-Temperature Alkali Chloride Molten Salts
- (2008) Ilya B. Polovov et al. INORGANIC CHEMISTRY
- Bond Multiplicity in Transition-Metal Complexes: Applications of Two-Electron Valence Indices
- (2008) Artur Michalak et al. JOURNAL OF PHYSICAL CHEMISTRY A
- Development of a low-temperature photoelectron spectroscopy instrument using an electrospray ion source and a cryogenically controlled ion trap
- (2008) Xue-Bin Wang et al. REVIEW OF SCIENTIFIC INSTRUMENTS
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started