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Reaction of the Pincer-type Ligand {2, 6-[P(O)(OEt)2]2-4-tert-Bu-C6H2}— with [Ph3C]+[PF6]—. Unprecedented Rearrangement and Carbon-Carbon Bond Formation

✍ Scribed by Markus Henn; Klaus Jurkschat; Ralf Ludwig; Michael Mehring; Katja Peveling; Markus Schürmann


Publisher
John Wiley and Sons
Year
2002
Tongue
German
Weight
160 KB
Volume
628
Category
Article
ISSN
0372-7874

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✦ Synopsis


The reaction of the organolithium derivative {2,6- ) which was characterized by 1 H, 13 C and 31 P NMR spectroscopy and single crystal X-ray analysis. Ab initio MO-calculations reveal the intramolecular O•••C distances in 5 of 2.952(4) and 2.988(5) A ˚being shorter than the sum of the van der Waals radii of oxygen and carbon to be the result ), welches 1 H-, 13 C-und 31 P-NMR-spektroskopisch und durch eine Einkristallröntgenstrukturanalyse charakterisiert wird. Ab initio MO-

Zur Reaktion des Zangenliganden {2,6-[P(O)(OEt


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Two New Carbon-Free Indium(III) Asymmetr
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The ligands [Ph 2 (S)PNHP(X)Ph 2 ] -(X = O, Se) react with InCl 3 coordination geometry in 2 resembles that observed in the three analogous tris-chelates incorporating the corres-in a 3:1 ratio to give a tris-chelate [In{Ph 2 P(O)NP(S)Ph 2 -O,S} 3 ]•0.75 C 6 H 6 (2) and the unexpected pentacoordinat