Osmium protonation/deprotonation

Osmium (continued) carbide, 24 233 dianion, lA. Xil, 317-319 with phosphines and diphosphines, 30 191 protonation/deprotonation, 30 169 raft hexaosmium clusters, 30 180-182 reactions of condensation, 30 145 with hexafluoroacetone, 30 288 redox, 30 184-185 structural transformations, 30 203 sulfur-containing, synthesis of, 30 147 sulfur derivatives, 24 269, 300-310 synthesis... 

Intermolecular addition of carbon nucleophiles to the ri2-pyrrolium complexes has shown limited success because of the decreased reactivity of the iminium moiety coupled with the acidity (pKa 18-20) of the ammine ligands on the osmium, the latter of which prohibits the use of robust nucleophiles. Addition of cyanide ion to the l-methyl-2//-pyr-rolium complex 32 occurs to give the 2-cyano-substituted 3-pyrroline complex 75 as one diastereomer (Figure 15). In contrast, the 1-methyl-3//-pyrrolium species 28, which possesses an acidic C-3-proton in an anti orientation, results in a significant (-30%) amount of deprotonation in addition to the 2-pyrroline complex 78 under the same reaction conditions. Uncharacteristically, 78 is isolated as a 3 2 ratio of isomers, presumably via epimerization at C-2.17 Other potential nucleophiles such as the conjugate base of malononitrile, potassium acetoacetate, and the silyl ketene acetal 2-methoxy-l-methyl-2-(trimethylsiloxy)-l-propene either do not react or result in deprotonation under ambient conditions. 

Figure 5.7 Schematic representation of the energy levels of a tetrazine-bridged osmium poly-pyridyl monolayer in the protonated and deprotonated states...

Several groups have completed computational studies on the relative stabilities of osmium carbyne, carbene, and vinylidene species. DFT calculations on the relative thermodynamic stability of the possible products from the reaction of OsH3Cl(PTr3)2 with a vinyl ether CH2=CH(OR) showed that the carbyne was favored. Ab initio calculations indicate that the vinylidene complex [CpOs(=C=CHR)L]+ is more stable than the acetylide, CpOs(-C=CR)L, or acetylene, [CpOs() -HC=CR)L]+, complexes but it doesn t form from these complexes spontaneously. The unsaturated osmium center in [CpOsL]+ oxidatively adds terminal alkynes to give [CpOsH(-C=CR)L]+. Deprotonation of the metal followed by protonation of the acetylide ligand gives the vinylidene product. 

The fluxional behavior of the osmium equivalents of the ruthenium(II) complexes mentioned in the final citation of the previous section has been described/ Time scales have been established for proton exchange at sulfur and at phosphorus in (26), R = Me or Et, and for deprotonation of (27) by the base DBU (1,8-diazabicyclo[5.4.0]undec-7-ene)/ ... 

Deprotonation of the species MCHj (M = Fe, Co) with a series of reference bases has been monitored, yielding the proton affinities of the corresponding carbene MCH2 species. Detailed kinetic studies have also been reported for the hydrogenation of the osmium alkyl bond in the complex (55) (L = PMea) [see Eq. (16)] which was shown to proceed by an acid-catalyzed path. ... 

Polymers containing benzimidazole units in their backbones have also been used in the synthesis of coordination metallopolymers (159-162). Osmium and ruthenium coordinated polymers with bipyridine ligands have been prepared (159,160). These polymers (72, 73) possessed metal-metal interactions through their conjugated backbones. Communication between the ruthenium centers of 72 increased by deprotonating the imidazole protons (160). The osmium coordinated polymer (73) showed two reduction waves separated by 0.32 V, indicative of strong cnmmimication between the Os centers (159). 

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