Conclusions
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1.
Based on the data obtained in studying the IR and13P NMR spectra of chromium η6- arenecarbonyl complexes with a diphosphine ligand, C5H5Cr (CO) (Ph2P (CH2)2PPh2) and (CH3)3C6H3-Cr(CO) (Ph2P(CH2)2PPh2), it was established that in acid media these complexes are protonated at the chromium atom to give the cis and trans isomers.
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2.
The deuterium exchange of C6H6Cr(CO)(Ph2P(CH2)2PPh2) in CF3COOD was studied and it was established that this complex exchanges hydrogen for deuterium at a rate that is 10 times slower than that of 1,3,5-(CH3)3C6H3Cr(CO)(Ph2P(CH2)2PPh2).
Literature cited
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2825–2828, December, 1983.
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Losilkina, V.I., Petrovskii, P.V., Baranetskaya, N.K. et al. Protonation and isotopic hydrogen exchange of chromium ν6-arenecarbonyl complexes with a diphosphine ligand in acid media. Russ Chem Bull 32, 2537–2539 (1983). https://doi.org/10.1007/BF00954489
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DOI: https://doi.org/10.1007/BF00954489