31P CP/MAS NMR of polycrystalline and immobilized phosphines and catalysts with fast sample spinning

被引:41
|
作者
Reinhard, S [1 ]
Blümel, J [1 ]
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词
NMR; P-31; CP/MAS; fast spinning; HH matching profiles; immobilized catalysts; immobilized phosphines; silica supports; rhodium and nickel catalysts;
D O I
10.1002/mrc.1183
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cross-polarization (CP) at fast magic angle spinning (MAS) frequencies leads to a splitting of the Hartmann-Hahn (HH) matching profile into a centerband and additional bands of higher orders. The matching profiles differ with the substance categories. Therefore, signal intensity is usually lost, when e.g. the routine standard NH4H2PO4 is used for optimizing the H-1-P-31 HH match prior to measuring phosphines and their metal complexes in polycrystalline or immobilized form. Here, a variety of model compounds, such as Ph2PCH2CH2PPh2 and (CO)(2)Ni(PPh3)(2), which can be used as P-31 CP standards for analogous substances or materials are presented. Investigating the influences of MAS frequency, contact time, H-1 pulse power and sample volume on the matching profiles of the model compounds leads to general trends. Thereby, a new strategy for measuring difficult samples with CP at high MAS rates has been developed: their optimum CP parameters are derived from the most intense maxima in the HH matching profiles of the corresponding model compounds. This new strategy is compared with variations of a conventional ramp sequence. Although the latter generally provide smaller signal half-widths, the new strategy leads to higher signal intensities. The new method was successfully applied to polycrystalline and immobilized phosphines and catalysts. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:406 / 416
页数:11
相关论文
共 50 条
  • [31] Polycrystalline and surface O,O′-dialkyldithiophosphate zinc(II) complexes:: preparation, 31P CP/MAS NMR and single-crystal X-ray diffraction studies
    Ivanov, AV
    Antzutkin, ON
    Larsson, AC
    Kritikos, M
    Forsling, W
    INORGANICA CHIMICA ACTA, 2001, 315 (01) : 26 - 35
  • [32] 31P solid-state NMR spectroscopy of VPO catalysts
    LI Mingxiu and YANG ShutaoDepartment of Chemistry
    ChineseScienceBulletin, 1997, (16) : 1370 - 1372
  • [33] 31P solid-state NMR spectroscopy of VPO catalysts
    Li, MX
    Yang, ST
    CHINESE SCIENCE BULLETIN, 1997, 42 (16): : 1370 - 1372
  • [34] Electrostatic screeening of membrane surfaces by high resolution 31P MAS NMR spectroscopy
    Lindström, F
    Bokvist, M
    Gröbner, G
    BIOPHYSICAL JOURNAL, 2002, 82 (01) : 3A - 4A
  • [35] An Approach to Probe Solid Electrolyte Interface on Si Anode by 31P MAS NMR
    Chen, Shoushun
    Zhong, Guiming
    Cao, Xia
    Gao, Yuxing
    Jin, Yanting
    Wu, Anan
    Gong, Zhengliang
    Fu, Riqiang
    Zhao, Yufen
    Yang, Yong
    ECS ELECTROCHEMISTRY LETTERS, 2013, 2 (12) : A115 - A117
  • [38] Quantification of crystalline phases and measurement of phosphate chain lengths in a mixed phase sample by 31P refocused INADEQUATE MAS NMR
    O'Dell, Luke A.
    Guerry, Paul
    Wong, Alan
    Abou Neel, Ensanya A.
    Pham, Tran N.
    Knowles, Jonathan C.
    Brown, Steven P.
    Smith, Mark E.
    CHEMICAL PHYSICS LETTERS, 2008, 455 (4-6) : 178 - 183
  • [39] Effect of cobalt-59 self-decoupling on the solid-state 31P CP/MAS NMR spectra of cobaloximes
    Schurko, Robert W.
    Wasylishen, Roderick E.
    Nelson, John H.
    Journal of physical chemistry, 1996, 100 (20): : 8053 - 8056
  • [40] 31P and 13C chemical shielding tensors in the phosphoenolpyruvate moiety from rotary resonance recoupling 13C and 31P MAS and single crystal 31P NMR
    Bechmann, M
    Dusold, S
    Förster, H
    Haeberlen, U
    Lis, T
    Sebald, A
    Stumber, M
    MOLECULAR PHYSICS, 2000, 98 (09) : 605 - 617