Experimental and quantum-chemical studies of 1H, 13C and 15N NMR coordination shifts in Pd(II) and Pt(II) chloride complexes with quinoline, isoquinoline, and 2,2'-biquinoline

Copyright (c) 2007 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 45(2007), 12 vom: 01. Dez., Seite 1059-71
1. Verfasser: Pazderski, Leszek (VerfasserIn)
Weitere Verfasser: Tousek, Jaromír, Sitkowski, Jerzy, Kozerski, Lech, Szłyk, Edward
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Carbon Isotopes Chlorides Isoquinolines Nitrogen Isotopes Organometallic Compounds Protons Quinolines 2,2'-biquinoline mehr... 119-91-5 Platinum 49DFR088MY Palladium 5TWQ1V240M quinoline E66400VT9R isoquinoline JGX76Y85M6
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245 1 0 |a Experimental and quantum-chemical studies of 1H, 13C and 15N NMR coordination shifts in Pd(II) and Pt(II) chloride complexes with quinoline, isoquinoline, and 2,2'-biquinoline 
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520 |a 1H, 13C, and 15N NMR studies of platinide(II) (M=Pd, Pt) chloride complexes with quinolines (L=quinoline-quin, or isoquinoline-isoquin; LL=2,2'-biquinoline-bquin), having the general formulae trans-/cis-[ML2Cl2] and [M(LL)Cl2], were performed and the respective chemical shifts (delta1H, delta13C, delta15N) reported. 1H coordination shifts of various signs and magnitudes (Delta1Hcoord=delta1Hcomplex-delta1Hligand) are discussed in relation to the changes of diamagnetic contribution to the relevant 1H shielding constants. The comparison to the literature data for similar complexes containing auxiliary ligands other than chlorides exhibited a large dependence of delta1H parameters on electron density variations and ring-current effects (inductive and anisotropic phenomena). The influence of deviations from planarity, concerning either MN2Cl2 chromophores or azine ring systems, revealed by the known X-ray structures of [Pd(bquin)Cl2] and [Pt(bquin)Cl2], is discussed in respect to 1H NMR spectra. 15N coordination shifts (Delta15Ncoord=delta15Ncomplex-delta15Nligand) of ca. 78-100 ppm (to lower frequency) are attributed mainly to the decrease of the absolute value of paramagnetic contribution in the relevant 15N shielding constants, this phenomenon being noticeably dependent on the type of a platinide metal and coordination sphere geometry. The absolute magnitude of Delta15Ncoord parameter increased by ca 15 ppm upon Pd(II)-->Pt(II) replacement but decreased by ca. 15 ppm following trans-->cis transition. Experimental 1H, 13C, 15N NMR chemical shifts are compared to those quantum-chemically calculated by B3LYP/LanL2DZ+6-31G**//B3LYP/LanL2DZ+6-31G*, both in vacuo and in CHCl3 or DMF solution 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Carbon Isotopes  |2 NLM 
650 7 |a Chlorides  |2 NLM 
650 7 |a Isoquinolines  |2 NLM 
650 7 |a Nitrogen Isotopes  |2 NLM 
650 7 |a Organometallic Compounds  |2 NLM 
650 7 |a Protons  |2 NLM 
650 7 |a Quinolines  |2 NLM 
650 7 |a 2,2'-biquinoline  |2 NLM 
650 7 |a 119-91-5  |2 NLM 
650 7 |a Platinum  |2 NLM 
650 7 |a 49DFR088MY  |2 NLM 
650 7 |a Palladium  |2 NLM 
650 7 |a 5TWQ1V240M  |2 NLM 
650 7 |a quinoline  |2 NLM 
650 7 |a E66400VT9R  |2 NLM 
650 7 |a isoquinoline  |2 NLM 
650 7 |a JGX76Y85M6  |2 NLM 
700 1 |a Tousek, Jaromír  |e verfasserin  |4 aut 
700 1 |a Sitkowski, Jerzy  |e verfasserin  |4 aut 
700 1 |a Kozerski, Lech  |e verfasserin  |4 aut 
700 1 |a Szłyk, Edward  |e verfasserin  |4 aut 
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