A fractional bond order of 1/2 in Pd25+ -: Formamidinate species; : The value of very high-field EPR spectra

被引:44
作者
Berry, John F.
Bill, Eckhard
Bothe, Eberhard
Cotton, F. Albert
Dalal, Naresh S.
Ibragimov, Sergey A.
Kaur, Narpinder
Liu, Chun Y.
Murillo, Carlos A.
Nellutla, Saritha
North, J. Micah
Villagran, Dino
机构
[1] Max Planck Inst Bioanorgan Chem, D-45470 Mulheim, Germany
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Florida State Univ, Natl High Magnet Field Lab, Dept Chem & Biochem, Tallahassee, FL 32306 USA
[4] Florida State Univ, Natl High Magnet Field Lab, Ctr Magnet Resonance, Tallahassee, FL 32306 USA
[5] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
[6] Texas A&M Univ, Lab Mol Struct & Bonding, College Stn, TX 77842 USA
关键词
D O I
10.1021/ja067328y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reaction of Pd-2(DAniF)(4), 1, (DAniF = di-p-anisylformamidinate) with 1 equiv of AgPF6 in CH2Cl2 at or below -10 degrees C produces the paramagnetic species [Pd-2(DAniF)(4)]PF6, 1-PF6, that has been studied by X-ray crystallography, UV-vis spectroscopy, electrochemistry, and multifrequency (9.5, 34.5, 110, and 220 GHz) EPR spectroscopy. Upon oxidation of the precursor, the Pd-Pd distance decreases by 0.052 angstrom from 2.6486(8) to 2.597(1) angstrom. The EPR spectra show broad signals with line widths of about 1000 G. The spectra collected at high field show a large spread of g tensor components (similar to 0.03), but these are masked at lower frequencies (9.5 and 34.5 GHz). A reinvestigation using high-field EPR of the p-tolyl analogue, which is the only other structurally characterized Pd-2(5+) species (Cotton, F. A.; Matusz, M.; Poli, R.; Feng, X. J. Am. Chem. Soc. 1988, 110, 1144), shows that this species, which had been reported to give an isotropic 9.5 GHz EPR spectrum, also gives anisotropic 110 and 220 GHz EPR spectra with a similarly large spread of g tensor components consistent with the unpaired electron residing in a metal-based MO. The results of these studies and calculations using density functional theory are consistent with the oxidation being metal-based, resulting in an uncommon Pd-2(5+) species with a Pd-Pd bond order of 1/2.
引用
收藏
页码:1393 / 1401
页数:9
相关论文
共 87 条
[1]   Examples of high-frequency EPR studies in bioinorganic chemistry [J].
Andersson, KK ;
Schmidt, PP ;
Katterle, B ;
Strand, KR ;
Palmer, AE ;
Lee, SK ;
Solomon, EI ;
Gräslund, A ;
Barra, AL .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2003, 8 (03) :235-247
[2]   ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 2ND AND 3RD ROW TRANSITION-ELEMENTS [J].
ANDRAE, D ;
HAUSSERMANN, U ;
DOLG, M ;
STOLL, H ;
PREUSS, H .
THEORETICA CHIMICA ACTA, 1990, 77 (02) :123-141
[3]   Divalent metal chloride amidine complexes .2. Compounds of Mn, Co and Ni [J].
Arnold, DI ;
Cotton, FA ;
Maloney, DJ ;
Matonic, JH .
POLYHEDRON, 1997, 16 (01) :133-141
[4]   UNUSUAL PARAMAGNETIC PLATINUM COMPLEXES - AN ELECTRON-SPIN-RESONANCE STUDY OF PLATINUM BLUES [J].
ARRIZABALAGA, P ;
CASTAN, P ;
GEOFFROY, M ;
LAURENT, JP .
INORGANIC CHEMISTRY, 1985, 24 (22) :3656-3660
[5]   SYNTHESIS AND CRYSTAL-STRUCTURE OF CIS-DIAMMINEPLATINUM ALPHA-PYRIDONE BLUE [J].
BARTON, JK ;
RABINOWITZ, HN ;
SZALDA, DJ ;
LIPPARD, SJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (08) :2827-2829
[6]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[7]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[8]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[9]   The Suzuki coupling of aryl chlorides in TBAB-water mixtures [J].
Bedford, RB ;
Blake, ME ;
Butts, CP ;
Holder, D .
CHEMICAL COMMUNICATIONS, 2003, (04) :466-467
[10]   Phenoxyl radicals hydrogen-bonded to imidazolium: Analogues of tyrosyl D of photosystem II: High-field EPR and DFT studies [J].
Benisvy, L ;
Bittl, R ;
Bothe, E ;
Garner, CD ;
McMaster, J ;
Ross, S ;
Teutloff, C ;
Neese, F .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (33) :5314-5317