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Frontispiece: From Phosphidic to Phosphonium? Umpolung of the P4-Bonding Situation in [CpFe(CO)(L)(η1-P4)]+ Cations (L=CO or PPh3)
Authors:Dr Ian M Riddlestone  Philippe Weis  Dr Arthur Martens  Marcel Schorpp  Dr Harald Scherer  Prof?Dr Ingo Krossing
Institution:Institut für Anorganische und Analytische Chemie and Freiburger Materialforschungszentrum (FMF), Universität Freiburg, Albertstr. 21, 79104 Freiburg, Germany
Abstract:Upon coordinating P4 to electron poor cyclopentadienyl-iron cations, the average P?P bond distances shrink and the respective P4 breathing mode in the Raman spectra (600 cm?1, P4, free) is blueshifted by >40 cm?1 in CpFe(CO)(L)(η1-P4)]+ cations (L=CO or PPh3). Analysis suggests that this corresponds to an umpolung of the bonding from more phosphidic in the known, electron-rich systems to more phosphonium-like in the reported electron-poor versions. This may open new functionalization pathways for white phosphorus P4.
Keywords:cations  clusters  iron  weakly coordinating anion (WCA)  white phosphorus (P4)
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