2000
DOI: 10.1016/s0020-1693(00)00287-5
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Syntheses and structural characterization of rhenium-bis-hydrazinopyrimidine core complexes with thiolate and Schiff base coligands

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Cited by 9 publications
(2 citation statements)
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“…Hence, the benzoyldiazenide ligand acts as a 3-electron donor (if considered in the neutral form a) or as a 4-electron donor (negatively charged form) [26], thus giving an 18-electron configuration to the complex. A similar coordination mode is known for a variety of organodiazenide rhenium complexes [11c, [27][28][29][30]. The average Re-Cl bond distance in compound 1 [2.4208 (19) Å ] is longer than that found in complex 3 (9) Bond angles Cl(1)-Re-Cl (2) 88.31 (6) Cl (1)-Re-Cl (2) 92.52 (14) Cl(1)-Re-P(1) 90.29 (5) Cl (1)-Re-P(1) 97.21(15) Cl(1)-Re-P (2) 89.45 (5) Cl (1) There is an intramolecular H bond N12-H12Á Á ÁO1 (H12Á Á ÁO1, 1.938 Å ) in 1 which implies the coplanarity of both the pyrazolyl and the organodiazenide groups.…”
Section: Solid State Structuressupporting
confidence: 55%
“…Hence, the benzoyldiazenide ligand acts as a 3-electron donor (if considered in the neutral form a) or as a 4-electron donor (negatively charged form) [26], thus giving an 18-electron configuration to the complex. A similar coordination mode is known for a variety of organodiazenide rhenium complexes [11c, [27][28][29][30]. The average Re-Cl bond distance in compound 1 [2.4208 (19) Å ] is longer than that found in complex 3 (9) Bond angles Cl(1)-Re-Cl (2) 88.31 (6) Cl (1)-Re-Cl (2) 92.52 (14) Cl(1)-Re-P(1) 90.29 (5) Cl (1)-Re-P(1) 97.21(15) Cl(1)-Re-P (2) 89.45 (5) Cl (1) There is an intramolecular H bond N12-H12Á Á ÁO1 (H12Á Á ÁO1, 1.938 Å ) in 1 which implies the coplanarity of both the pyrazolyl and the organodiazenide groups.…”
Section: Solid State Structuressupporting
confidence: 55%
“…Ligand L is a general Lewis base, PAr 3 , pyridine, tetramethylthiourea, R 2 S, and so forth, and the dt ligands include 1,2-ethanedithiolate (edt), 1,3-propanedithiolate (pdt), and mtp, the dianion of 2-(mercaptomethyl)thiophenol. Compounds lacking a Me−Re bond include [(ReO) 2 (mtp) 3 ] and others that have been described by Zubieta and et al and Abu-Omar et al Both monomers and, especially, dimers catalyze OAT reactions, ,, YO + X → Y + XO, for which combinations of YO (e.g., C 5 H 5 NO, tert -BuOOH, R 2 SO) have been used, their reaction partners X being, for example, PAr 3 , R 2 S, and R 2 SO.…”
Section: Introductionmentioning
confidence: 99%