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A novel Ta/Os heterobimetallic complex, [Ta(CH2tBu)3(μ-H)3OsCp*], 2, is prepared by protonolysis of Ta(CHtBu)(CH2tBu)3 with Cp*OsH5. Treatment of 2 and its iridium analogue [Ta(CH2tBu)3(μ-H)2IrCp*], 1, with CO2 under mild conditions reveal the efficient cleavage of CO2, driven by the formation of a tantalum oxo species in conjunction with CO transfer to the osmium or iridium fragments, to form Cp*Ir(CO)H2 and Cp*Os(CO)H3, respectively. This bimetallic reactivity diverges from more classical CO2 insertion into metal–X (X = metal, hydride, alkyl) bonds. [ABSTRACT FROM AUTHOR]

Polynuclear metal hydride clusters play important roles in various catalytic processes, with most of the reported polynuclear metal hydride clusters adopting a polyhedral three‐dimensional structure. Herein, we report the first example of a planar tetranuclear uranium hydride cluster [(CpCMe2CMe2Cp)U]4(μ2‐H)4(μ3‐H)4 (U4H8). It was synthesized by reacting an ansa‐bis(cyclopentadienyl) ligand‐supported uranium chloride precursor [(CpCMe2CMe2Cp)U]3(μ2‐Cl)3(μ3‐Cl)2 with NaHBEt3. The presence of hydrides in U4H8 was confirmed by NMR spectroscopy and its reactivity with phenol and carbon tetrachloride. DFT calculations also facilitated the determination of the hydrides' positions in U4H8, featuring four bridging μ2‐H ligands and four face‐capping μ3‐H ligands, with the four U centers arranged in a rhombic geometry. The U4H8 represents not only the first example of planar polynuclear actinide metal hydride cluster but also the uranium hydride cluster with the highest nuclearity reported to date. [ABSTRACT FROM AUTHOR]

Reduction of a range of amido‐ and aryloxy‐aluminum dihydride complexes, e.g. [AlH2(NR3){N(SiMe3)2}] (NR3=NMe3 or N‐methylpiperidine (NMP)), with β‐diketiminato dimagnesium(I) reagents, [{(ArNacnac)Mg}2] (ArNacnac=[HC(MeCNAr)2]−, Ar=mesityl (Mes) or 2,6‐xylyl (Xyl)), have afforded deep red mixed valence aluminum hydride cluster compounds, [Al6H8(NR3)2{Mg(ArNacnac)}4], which have an average Al oxidation state of +0.66, the lowest for any well‐defined aluminum hydride compound. In the solid‐state, the clusters are shown to have distorted octahedral Al6 cores, having zero‐valent Al axial sites and mono‐valent AlH2− equatorial units. Several novel by‐products were isolated from the reactions that gave the clusters, including the Mg−Al bonded magnesio‐aluminate complexes, [(ArNacnac)(Me3N)Mg−Al(μ‐H)3[{Mg(ArNacnac)}2(μ‐H)]]. Computational analyses of one aluminum hydride cluster revealed its Al6 core to be electronically delocalized, and to possess one unoccupied, and six occupied, skeletal molecular orbitals. [ABSTRACT FROM AUTHOR]

Reduction of a range of amido‐ and aryloxy‐aluminum dihydride complexes, e.g. [AlH2(NR3){N(SiMe3)2}] (NR3=NMe3 or N‐methylpiperidine (NMP)), with β‐diketiminato dimagnesium(I) reagents, [{(ArNacnac)Mg}2] (ArNacnac=[HC(MeCNAr)2]−, Ar=mesityl (Mes) or 2,6‐xylyl (Xyl)), have afforded deep red mixed valence aluminum hydride cluster compounds, [Al6H8(NR3)2{Mg(ArNacnac)}4], which have an average Al oxidation state of +0.66, the lowest for any well‐defined aluminum hydride compound. In the solid‐state, the clusters are shown to have distorted octahedral Al6 cores, having zero‐valent Al axial sites and mono‐valent AlH2− equatorial units. Several novel by‐products were isolated from the reactions that gave the clusters, including the Mg−Al bonded magnesio‐aluminate complexes, [(ArNacnac)(Me3N)Mg−Al(μ‐H)3[{Mg(ArNacnac)}2(μ‐H)]]. Computational analyses of one aluminum hydride cluster revealed its Al6 core to be electronically delocalized, and to possess one unoccupied, and six occupied, skeletal molecular orbitals. [ABSTRACT FROM AUTHOR]

Hydrogenolysis of the half-sandwich penta-arylcycopentadienyl-supported rare-earth metal dibenzyl complexes [(CpAr5)Ln(p-CH2-C6H4-Me)2(THF)] (CpAr5 = C5Ar5, Ar = 3,5-iPr2-C6H3; Ln = Sc, La) afforded a bimetallic scandium complex [(CpAr5)Sc(H)(μ-OC4H9)]2 (2) with two terminal hydrido ligands, and a double-sandwich bimetallic lanthanum hydride complex [(CpAr5)La(μ-H)]2 (4) bearing the reduced CpAr5 ligand. DFT calculations were conducted to elucidate the reaction profiles. [ABSTRACT FROM AUTHOR]

Hydrogenolysis of alkyl‐substituted cyclopentadienyl (CpR) ligated thorium tribenzyl complexes [(CpR)Th(p‐CH2‐C6H4‐Me)3] (1–6) afforded the first examples of molecular thorium trihydrido complexes [(CpR)Th(μ‐H)3]n (CpR=C5H2(tBu)3 or C5H2(SiMe3)3, n=5; C5Me4SiMe3, n=6; C5Me5, n=7; C5Me4H, n=8; 7–10 and 12) and [(Cp#)12Th13H40] (Cp#=C5H4SiMe3; 13). The nuclearity of the metal hydride clusters depends on the steric profile of the cyclopentadienyl ligands. The hydrogenolysis intermediate, tetra‐nuclear octahydrido thorium dibenzylidene complex [(Cpttt)Th(μ‐H)2]4(μ‐p‐CH‐C6H4‐Me)2 (Cpttt=C5H2(tBu)3) (11) was also isolated. All of the complexes were characterized by NMR spectroscopy and single‐crystal X‐ray analysis. Hydride positions in [(CpMe4)Th(μ‐H)3]8 (CpMe4=C5Me4H) were further precisely confirmed by single‐crystal neutron diffraction. DFT calculations strengthen the experimental assignment of the hydride positions in the complexes 7 to 12. [ABSTRACT FROM AUTHOR]

• Two routes to prepare Ta-Ir/SiO 2 catalysts via surface organometallic chemistry. • In-depth structural characterization of Ta, Ta-Ir and Ta-Ir 2 surface sites. • Improved catalytic performances in H/D isotope exchange and propane metathesis. A stepwise surface organometallic chemistry (SOMC) methodology consisting in using a silica-supported tantalum species, [(≡SiO)Ta(CH t Bu)(CH 2 t Bu) 2 ], as a reactive center to coordinate an iridium site, was developed to construct tantalum/iridium heterobimetallic edifices. The resulting material, MAT-2 , exhibits enhanced catalytic performances - both in H/D isotopic exchange and alkane metathesis reactions - in comparison to MAT-1 , which was prepared from the direct grafting on silica of a well-defined heterobimetallic Ta/Ir complex. We projected that the difference in catalytic activity was due to the presence of distinct active sites and we used a combination of advanced spectroscopic methods (IR, solid-state NMR and XAS spectroscopies) as well as modeling (computational studies and molecular models) to identify the structure of these surface species. These investigations point towards the presence of three types of active sites at the surface of MAT-2 : the heterobimetallic surface species, [≡SiOTa(CH 2 t Bu) 2 {IrH 2 (Cp*)}] 2-s , which is also found in MAT-1 , as well as an unanticipated heterotrimetallic species, [≡SiOTa(CH 2 t Bu) 2 {IrH 2 (Cp*)}], 3-s along with some unreacted monometallic Ta sites [(≡SiO)Ta(CH t Bu)(CH 2 t Bu) 2 ], 1-s. The well-defined trimetallic surface species 3-s was independently prepared and characterized to support this hypothesis. This study highlights the importance of the synthetic methodology used for the preparation of heterobimetallic species through SOMC, and the difficulty to obtain true single-sites surface species. [ABSTRACT FROM AUTHOR]

Reduction of a range of amido‐ and aryloxy‐aluminum dihydride complexes, e.g. [AlH2(NR3){N(SiMe3)2}] (NR3=NMe3 or N‐methylpiperidine (NMP)), with β‐diketiminato dimagnesium(I) reagents, [{(ArNacnac)Mg}2] (ArNacnac=[HC(MeCNAr)2]−, Ar=mesityl (Mes) or 2,6‐xylyl (Xyl)), have afforded deep red mixed valence aluminum hydride cluster compounds, [Al6H8(NR3)2{Mg(ArNacnac)}4], which have an average Al oxidation state of +0.66, the lowest for any well‐defined aluminum hydride compound. In the solid‐state, the clusters are shown to have distorted octahedral Al6 cores, having zero‐valent Al axial sites and mono‐valent AlH2− equatorial units. Several novel by‐products were isolated from the reactions that gave the clusters, including the Mg−Al bonded magnesio‐aluminate complexes, [(ArNacnac)(Me3N)Mg−Al(μ‐H)3[{Mg(ArNacnac)}2(μ‐H)]]. Computational analyses of one aluminum hydride cluster revealed its Al6 core to be electronically delocalized, and to possess one unoccupied, and six occupied, skeletal molecular orbitals. [ABSTRACT FROM AUTHOR]

Reduction of a range of amido‐ and aryloxy‐aluminum dihydride complexes, e.g. [AlH2(NR3){N(SiMe3)2}] (NR3=NMe3 or N‐methylpiperidine (NMP)), with β‐diketiminato dimagnesium(I) reagents, [{(ArNacnac)Mg}2] (ArNacnac=[HC(MeCNAr)2]−, Ar=mesityl (Mes) or 2,6‐xylyl (Xyl)), have afforded deep red mixed valence aluminum hydride cluster compounds, [Al6H8(NR3)2{Mg(ArNacnac)}4], which have an average Al oxidation state of +0.66, the lowest for any well‐defined aluminum hydride compound. In the solid‐state, the clusters are shown to have distorted octahedral Al6 cores, having zero‐valent Al axial sites and mono‐valent AlH2− equatorial units. Several novel by‐products were isolated from the reactions that gave the clusters, including the Mg−Al bonded magnesio‐aluminate complexes, [(ArNacnac)(Me3N)Mg−Al(μ‐H)3[{Mg(ArNacnac)}2(μ‐H)]]. Computational analyses of one aluminum hydride cluster revealed its Al6 core to be electronically delocalized, and to possess one unoccupied, and six occupied, skeletal molecular orbitals. [ABSTRACT FROM AUTHOR]

The article discusses the result of a study concerning rare earth metal alkyl and hydride complexes stabilized by a cyclen-driven macrocyclic ancillary ligand. Me3TACD ligand was introduced as a monoanionic ancillary environment for the stabilization of rare earth metal alkyl and hydride with properties distinct from other monoanionic ligands.