22 research outputs found
Organometallic derivatives of Rh- and Ir-substituted polyoxotungstates with Keggin structure: reactivity screening by electrospray ionization mass-spectrometry
ESI-MS based methodology for the rapid reactivity screening of [PW11O39RhCl]5− and [PW11O39Ir(H2O)]4− toward various metalation-intended substrates (reagents with an activated C–H bond, boronic acids and organotin compounds) is presented. Formation of a series of new organometallic POM derivatives with Rh–R (R = malonate, phenylacetate, CH3, Ph, ferrocenyl) and Ir–R (R = CH3) bonds is reported
New {RuNO} Polyoxometalate [PW11O39RuII(NO)]4-: Synthesis and Reactivity
New Ru-containing polyoxometalate [PW11O39RuII(NO)]4- (14-) was obtained in high yield by reaction of [Ru(NO)Cl5]2- with [PW11O39]7- and characterized by multinuclear NMR, cyclic voltammetry, IR spectroscopy, and electrospray ionization mass spectrometry (ESI-MS). The intrinsic reactivity of the {RuNO} site in 14- toward various reagents has been studied using a versatile and simple ESI tandem mass spectrometric methodology for identification of the L attached at the Ru site; this approach relies on the preferential liberation of the L ligands attached at the Ru sites upon mass-selecting desired intermediates and subsequent promotion of their fragmentation. Reactions with both hydrazine and hydroxylamine lead to elimination of the nitroso group and quantitative formation of [PW11O39RuIII(H2O)]4- (24-) in aqueous solution. In the reaction with hydroxylamine, an intermediate with coordinated dinitrogen has been detected. An easy access to the NH3-coordinated [PW11O39RuNH3]4- (34-) complex was achieved upon reduction of 14- with Sn2+ in water
New {RuNO} Polyoxometalate [PW<sub>11</sub>O<sub>39</sub>Ru<sup>II</sup>(NO)]<sup>4‑</sup>: Synthesis and Reactivity
New Ru-containing
polyoxometalate [PW<sub>11</sub>O<sub>39</sub>Ru<sup>II</sup>(NO)]<sup>4‑</sup> (<b>1</b><sup>4‑</sup>) was obtained
in high yield by reaction of [RuÂ(NO)ÂCl<sub>5</sub>]<sup>2‑</sup> with [PW<sub>11</sub>O<sub>39</sub>]<sup>7‑</sup> and characterized
by multinuclear NMR, cyclic voltammetry, IR spectroscopy, and electrospray
ionization mass spectrometry (ESI-MS). The intrinsic reactivity of
the {RuNO} site in <b>1</b><sup>4‑</sup> toward various
reagents has been studied using a versatile and simple ESI tandem
mass spectrometric methodology for identification of the L attached
at the Ru site; this approach relies on the preferential liberation
of the L ligands attached at the Ru sites upon mass-selecting desired
intermediates and subsequent promotion of their fragmentation. Reactions
with both hydrazine and hydroxylamine lead to elimination of the nitroso
group and quantitative formation of [PW<sub>11</sub>O<sub>39</sub>Ru<sup>III</sup>(H<sub>2</sub>O)]<sup>4‑</sup> (<b>2</b><sup>4‑</sup>) in aqueous solution. In the reaction with hydroxylamine,
an intermediate with coordinated dinitrogen has been detected. An
easy access to the NH<sub>3</sub>-coordinated [PW<sub>11</sub>O<sub>39</sub>RuNH<sub>3</sub>]<sup>4‑</sup> (<b>3</b><sup>4‑</sup>) complex was achieved upon reduction of <b>1</b><sup>4‑</sup> with Sn<sup>2+</sup> in water