Palladium K-edge X-ray Absorption Spectroscopy Studies on Controlled Ligand Systems

被引:0
作者
Westawker, Luke P. [1 ]
Khusnutdinova, Julia K. [2 ]
Wallick, Rachel F. [1 ]
Mirica, Liviu M. [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Okinawa Inst Sci & Technol Grad Univ, Coordinat Chem & Catalysis Unit, Onna Son, Okinawa 9040495, Japan
基金
美国国家科学基金会;
关键词
OXIDATION-STATE; ORGANOMETALLIC PD(III); DIMETHYL COMPLEX; LOCAL-STRUCTURE; REACTIVITY; XAS; XANES; EXAFS; CHEMISTRY; CATALYSTS;
D O I
10.1021/acs.inorgchem.3c03032
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
X-ray absorption spectroscopy (XAS) is widely used across the life and physical sciences to identify the electronic properties and structure surrounding a specific element. XAS is less often used for the characterization of organometallic compounds, especially for sensitive and highly reactive species. In this study, we used solid- and solution-phase XAS to compare a series of 25 palladium complexes in controlled ligand environments. The compounds include palladium centers in the formal I, II, III, and IV oxidation states, supported by tridentate and tetradentate macrocyclic ligands, with different halide and methyl ligand combinations. The Pd K-edge energies increased not only upon oxidizing the metal center but also upon increasing the denticity of the ligand framework, substituting sigma-donating methyl groups with chlorides, and increasing the charge of the overall metal complex by replacing charged ligands with neutral ligands. These trends were then applied to characterize compounds whose oxidation states were otherwise unconfirmed.
引用
收藏
页码:21128 / 21137
页数:10
相关论文
共 50 条
  • [2] Identification of Uranyl Minerals Using Oxygen K-Edge X-Ray Absorption Spectroscopy
    Ward, Jesse D.
    Bowden, Mark
    Resch, C. Tom
    Smith, Steven
    McNamara, Bruce K.
    Buck, Edgar C.
    Eiden, Gregory C.
    Duffin, Andrew M.
    GEOSTANDARDS AND GEOANALYTICAL RESEARCH, 2016, 40 (01) : 135 - 148
  • [3] Iodine species uptake by cement and CSH studied by I K-edge X-ray absorption spectroscopy
    Bonhoure, I
    Scheidegger, AM
    Wieland, E
    Dähn, R
    RADIOCHIMICA ACTA, 2002, 90 (9-11) : 647 - 651
  • [4] X-ray absorption in atomic iodine in the K-edge region
    Gomilsek, J. Padeznik
    Arcon, I.
    de Panfilis, S.
    Kodre, A.
    PHYSICAL REVIEW A, 2009, 79 (03):
  • [5] Indium and Nitrogen K-edge X-Ray Absorption Spectroscopy of InxGa1-xN
    Li, Xianya
    Chang, Chieh Miao
    Hsueh, Chih-Han
    Lee, Zyh-Fu
    Chen, Jin-Ming
    Lin, Hao-Hsiung
    Wang, Xingiang
    Dietz, Nikolaus
    Guan Yong-Jing
    Feng, Zhe Chuan
    2016 5TH INTERNATIONAL SYMPOSIUM ON NEXT-GENERATION ELECTRONICS (ISNE), 2016,
  • [6] Iridium L3-edge and oxygen K-edge x-ray absorption spectroscopy of nanocrystalline iridium oxide thin films
    Kuzmin, A
    Kalendarev, R
    Purans, J
    Pailharey, D
    ADVANCED OPTICAL DEVICES, TECHNOLOGIES, AND MEDICAL APPLICATIONS, 2002, 5123 : 210 - 214
  • [7] Understanding Copper(I)-Ethylene Bonding Using Cu K-Edge X-ray Absorption Spectroscopy
    Asundi, Arun S.
    Noonikara-Poyil, Anurag
    Phan, Vo Quang Huy
    Dias, H. V. Rasika
    Sarangi, Ritimukta
    INORGANIC CHEMISTRY, 2023, 62 (47) : 19298 - 19311
  • [8] Scrutinizing metal-ligand covalency and redox non-innocence via nitrogen K-edge X-ray absorption spectroscopy
    Lukens, James T.
    DiMucci, Ida M.
    Kurogi, Takashi
    Mindiola, Daniel J.
    Lancaster, Kyle M.
    CHEMICAL SCIENCE, 2019, 10 (19) : 5044 - 5055
  • [9] Electronic structure of S-nitrosothiols from sulfur K-edge X-ray absorption spectroscopy
    Martin-Diaconescu, Vlad
    Perepichka, Inna
    Bohle, D. Scott
    Kennepohl, Pierre
    CANADIAN JOURNAL OF CHEMISTRY, 2011, 89 (02) : 93 - 97
  • [10] X-ray Absorption Spectroscopy at the Sulfur K-Edge: A New Tool to Investigate the Biochemical Mechanisms of Neurodegeneration
    Hackett, Mark J.
    Smith, Shari E.
    Paterson, Phyllis G.
    Nichol, Helen
    Pickering, Ingrid J.
    George, Graham N.
    ACS CHEMICAL NEUROSCIENCE, 2012, 3 (03): : 178 - 185