2007
DOI: 10.3998/ark.5550190.0009.505
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Synthesis and crystal structures of cis-palladium(II) and cis-platinum(II) complexes containing dipyridyl ligands

Abstract: Coordinative behavior of the di-(2-pyridyl)hydroxymethane (1) and di-(2-pyridyl)-2-pyridylsulfanylmethane (2) ligands towards Pd(II) and Pt(II) is described. The compounds 3-5 were characterized by IR, mass spectrometry and NMR spectroscopy. Crystal structures of [Pt{(C 5 H 4 N) 2 CH(OH)}Cl 2 ] 3 and [Pd{(C 5 H 4 N) 2 CH(2-C 5 H 4 NS)}Cl 2 ] 4 as DMSO solvates displayed the formation of neutral mononuclear complexes. In the complexes 3 and 4 is observed the formation of six-membered chelate rings. The local ge… Show more

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Cited by 2 publications
(8 citation statements)
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“…This angle, defined as the Pt–N–centroid angle (N = N1 or N3, centroid = aromatic ring center) should approach ∼180°. The Pt–N–centroid angle ranges from 164–180° for known Pt­(II) complexes of imidazolyl or pyridyl ligands bound in a monodentate, bidentate, or tridentate fashion. , This angle averages 174.5° for 5 (Table ), which is similar to the value for monodentate ligands (176.7°; see the Supporting Information); this is another indication that the pyridyl rings in 5 are well-positioned to form a strong Pt–N bond.…”
Section: Resultsmentioning
confidence: 72%
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“…This angle, defined as the Pt–N–centroid angle (N = N1 or N3, centroid = aromatic ring center) should approach ∼180°. The Pt–N–centroid angle ranges from 164–180° for known Pt­(II) complexes of imidazolyl or pyridyl ligands bound in a monodentate, bidentate, or tridentate fashion. , This angle averages 174.5° for 5 (Table ), which is similar to the value for monodentate ligands (176.7°; see the Supporting Information); this is another indication that the pyridyl rings in 5 are well-positioned to form a strong Pt–N bond.…”
Section: Resultsmentioning
confidence: 72%
“…The N1–Pt–N3 bite angle of 5 (87.98°) is at the high end of the range reported for Pt­(II) complexes with mono- or bidentate-coordinated ligands terminated by pyridyl or imidazolyl rings (78–91°). The bite angles of known Pt complexes having eight-membered chelate rings (average 89.5°) are higher than for Pt complexes with smaller chelate rings but are quite close to those for monodentate complexes (average 89.4°) (Figure ). We attribute this finding to the greater spatial freedom provided by the larger chelate ring; this freedom allows the N-donor rings to be located in the same relative position as monodentate ligands.…”
Section: Resultsmentioning
confidence: 77%
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