1973
DOI: 10.1021/ja00798a018
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Synthesis, chemistry, and spectroscopy of some tris(pentahapto-cyclopentadienyl)uranium(IV) alkyl and aryl compounds

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Cited by 154 publications
(58 citation statements)
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“…The calculated IR frequencies for X = Ph complex are shown in Table 3b. It was confirmed by the vector analysis of normal vibration modes that the vibrational frequencies of 1200-1300 and 1400-1600 cm -1 are assigned to the vibrations attributed to Ph -ligand, being consistent with the corresponding experimental frequencies [29] (Table 3b). Because stretching vibration frequency of aromatic C=C bond is in this region, Ph -ligand in complex remains to have an aromaticity.…”
Section: Equilibrium Structures Of Cp3np IV Xsupporting
confidence: 86%
“…The calculated IR frequencies for X = Ph complex are shown in Table 3b. It was confirmed by the vector analysis of normal vibration modes that the vibrational frequencies of 1200-1300 and 1400-1600 cm -1 are assigned to the vibrations attributed to Ph -ligand, being consistent with the corresponding experimental frequencies [29] (Table 3b). Because stretching vibration frequency of aromatic C=C bond is in this region, Ph -ligand in complex remains to have an aromaticity.…”
Section: Equilibrium Structures Of Cp3np IV Xsupporting
confidence: 86%
“…The terminal η 3 -allyl protons were not observed in previously reported U[η 3 -CH 2 C(R)CH 2 ] complexes, and only the vinyl protons are observable in (C 5 H 5 ) 3 U(η 1 -CH 2 CHCH 2 ). 19 Protons on carbon atoms α to U 4+ are often not observed due to the paramagnetic nature of 5f 2 U 4+ . 40 For example, no resonances are observed for the α carbon protons in (η 5 -C 5 Me 4 SiMe 2 CH 2 -κC) 2 U, whereas they appear in derivatives in which a single atom has been inserted between the α carbons and the metal.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…Thus, it was three decades after the Manhattan Project studies before the first thermally stable actinide alkyls, aryls, alkenyls, and alkynyls (collectively called hydrocarbyls) were synthesized (Eq. 13) (17,34,35). In …”
Section: Actinide-carbon Sigma Bonds; Synthesismentioning
confidence: 99%
“…The explanation appears to reside in the high coordinative saturation and congestion brought about by the three bulky, r-bonded cyclopentadienyl ligands (34). Evidence for this comes from the short intraligand nonbonded contacts found in x-ray diffraction studies and hindered rotation about the M-R bonds observed in spectroscopic work (34).…”
Section: Actinide-carbon Sigma Bonds; Synthesismentioning
confidence: 99%