Synthesis of bis(2-pyridylthio)methyl zinc hydride and catalytic hydrosilylation and hydroboration of CO2.

The reactions of bis(2-pyridylthio)methane with Me2Zn and Zn[N(SiMe3)2]2 afford [Bptm]ZnMe and [Bptm]ZnN(SiMe3)2, thereby providing access to a variety of other [Bptm]ZnX derivatives, including the zinc hydride complex [Bptm]ZnH, which serves as a catalyst for the reduction of CO2 and other carbonyl compounds via hydrosilylation and hydroboration.

Catalytic reduction of carbon dioxide by a zinc hydride compound, [Tptm]ZnH, and conversion to the methanol level.

The zinc hydride compound, [Tptm]ZnH, may achieve the reduction of CO2 by (RO)3SiH (R = Me, Et) to the methanol oxidation level, (MeO)xSi(OR)4-x, via the formate species, HCO2Si(OR)3. However, because insertion of CO2 into the Zn-H bond is more facile than insertion of HCO2Si(OR)3, conversion of HCO2Si(OR)3 to the methanol level only occurs to a significant extent in the absence of CO2.

Rhenium versus cadmium: an alternative structure for a thermally stable cadmium carbonyl compound.

An alternative description is provided for the previously reported novel tetranuclear cadmium carbonyl compound, [Cd(CO)3(C6H3Cl)]4. Specifically, consideration of single crystal X-ray diffraction data indicates that the compound is better formulated as the rhenium compound, [Re(CO)3(C4N2H3S)]4. Furthermore, density functional theory calculations predict that, if it were to exist, [Cd(CO)3(C6H3Cl)]4 would have a very different structure to that reported. While it is well known that X-ray diffraction may not reliably distinguish between atoms of similar atomic number (e.g. N/C and Cl/S), it is not generally recognized that two atoms with very different atomic numbers could be misassigned. The misidentification of two elements as diverse as Re and Cd (ΔZ = 27) is unexpected and serves as an important caveat for structure determinations.

Reactivity of the carbodiphosphorane, (Ph3P)2C, towards main group metal alkyl compounds: coordination and cyclometalation.

The carbodiphosphorane, (Ph3P)2C, reacts with Me3Al and Me3Ga to afford the adducts, [(Ph3P)2C]AlMe3 and [(Ph3P)2C]GaMe3, which have been structurally characterized by X-ray diffraction. (Ph3P)2C also reacts with Me2Zn and Me2Cd to generate an adduct but the formation is reversible on the NMR time scale. At elevated temperatures, however, elimination of methane and cyclometalation occurs to afford [κ2-Ph3PC{PPh2(C6H4)}]ZnMe and [κ2-Ph3PC{PPh2(C6H4)}]CdMe. Analogous cyclometalated products, [κ2-Ph3P{CPPh2(C6H4)}]ZnN(SiMe3)2 and [κ2-Ph3P{CPPh2(C6H4)}]CdN(SiMe3)2, are also obtained upon reaction of (Ph3P)2C with Zn[N(SiMe3)2]2 and Cd[N(SiMe3)2]2. The magnesium compounds, Me2Mg and {Mg[N(SiMe3)2]2}2, likewise react with (Ph3P)2C to afford cyclometalated derivatives, namely [κ2-Ph3PC{PPh2(C6H4)}]MgN(SiMe3)2 and {[κ2-Ph3PC{PPh2(C6H4)}]MgMe}2. While this reactivity is similar to the zinc system, the magnesium methyl complex is a dimer with bridging methyl groups, whereas the zinc complex is a monomer. The greater tendency of the methyl groups to bridge magnesium centers rather than zinc centers is supported by density functional theory calculations.

Impairment of Excitation-Contraction Coupling in Right Ventricular Hypertrophied Muscle with Fibrosis Induced by Pulmonary Artery Banding.

Interstitial myocardial fibrosis is one of the factors responsible for dysfunction of the heart. However, how interstitial fibrosis affects cardiac function and excitation-contraction coupling (E-C coupling) has not yet been clarified. We developed an animal model of right ventricular (RV) hypertrophy with fibrosis by pulmonary artery (PA) banding in rats. Two, four, and six weeks after the PA-banding operation, the tension and intracellular Ca2+ concentration of RV papillary muscles were simultaneously measured (n = 33). The PA-banding rats were clearly divided into two groups by the presence or absence of apparent interstitial fibrosis in the papillary muscles: F+ or F- group, respectively. The papillary muscle diameter and size of myocytes were almost identical between F+ and F-, although the RV free wall weight was heavier in F+ than in F-. F+ papillary muscles exhibited higher stiffness, lower active tension, and lower Ca2+ responsiveness compared with Sham and F- papillary muscles. In addition, we found that the time to peak Ca2+ had the highest correlation coefficient to percent of fibrosis among other parameters, such as RV weight and active tension of papillary muscles. The phosphorylation level of troponin I in F+ was significantly higher than that in Sham and F-, which supports the idea of lower Ca2+ responsiveness in F+. We also found that connexin 43 in F+ was sparse and disorganized in the intercalated disk area where interstitial fibrosis strongly developed. In the present study, the RV papillary muscles obtained from the PA-banding rats enabled us to directly investigate the relationship between fibrosis and cardiac dysfunction, the impairment of E-C coupling in particular. Our results suggest that interstitial fibrosis worsens cardiac function due to 1) the decrease in Ca2+ responsiveness and 2) the asynchronous activation of each cardiac myocyte in the fibrotic preparation due to sparse cell-to-cell communication.

Tertiary Structure-Based Prediction of How ATRP Initiators React with Proteins.

The growth of polymers from the surface of proteins via controlled radical polymerization depends on the attachment of small molecule initiators to amino acid residues. Our ability to control and harness the power of polymer-based protein engineering is reliant on the accuracy of prediction where and how fast atom transfer radical polymerization (ATRP) initiators will react with a protein surface. We performed a systematic characterization of the reaction between a bromine-functionalized N-hydroxysuccinimide amine-reactive ATRP initiator and the amino groups in lysozyme and chymotrypsin. The tertiary structures of the proteins were used to predict computationally α-amino group and lysine side-chain accessibility and analyze the chemical and structural environment of the amino groups. To predict reactivity from accessibility calculations, a probe radius that resembled the size of the initiator molecule was used. Experimental data showed that the rate of initiator-protein modification at each amine site was related to surface accessibility but not the pKa of amino groups. Further refinements of the prediction of where the initiator modified the protein and in what sequence were achieved by considering the local environment of each amino group.