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The reactivity of a diruthenium tetrahydride complex towards three selected dihydroboranes was investigated. The use of [DurBH 2 ] (Dur=2,3,5,6-Me 4 C 6 H) and [(Me 3 Si) 2 NBH 2 ] led to the formation of bridging borylene complexes of the form [(Cp*RuH) 2 BR] (Cp*=C 5 Me 5 ; 1 a: R=Dur; 1 b: R=N(SiMe 3 ) 2 ) through oxidative addition of the B-H bonds with concomitant hydrogen liberation. Employing the more electron-deficient dihydroborane [3,5-(CF 3 ) 2 -C 6 H 3 BH 2 ] led to the formation of an anionic complex bearing a tetraarylated chain of four boron atoms, namely Li(THF) 4 [(Cp*Ru) 2 B 4 H 5 (3,5-(CF 3 ) 2 C 6 H 3 ) 4 ] (4), through an unusual, incomplete threefold dehydrocoupling process. A comparative theoretical investigation of the bonding in a simplified model of 4 and the analogous complex nido-[1,2(Cp*Ru) 2 (μ-H)B 4 H 9 ] (I) indicates that there appear to be no classical σ-bonds between the boron atoms in complex I, whereas in the case of 4 the B 4 chain better resembles a network of three B-B σ bonds, the central bond being significantly weaker than the other two., (© 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)

The steric and electronic properties of aryl substituents in monoaryl borohydrides (Li[ArBH 3 ]) and dihydroboranes were systematically varied and their reactions with [Ru(PCy 3 ) 2 HCl(H 2 )] (Cy: cyclohexyl) were studied, resulting in bis(σ)-borane or terminal borylene complexes of ruthenium. These variations allowed for the investigation of the factors involved in the activation of dihydroboranes in the synthesis of terminal borylene complexes. The complexes were studied by multinuclear NMR spectroscopy, mass spectrometry, X-ray diffraction analysis, and density functional theory (DFT) calculations. The experimental and computational results suggest that the ortho-substitution of the aryl groups is necessary for the formation of terminal borylene complexes., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A series of bis(σ)-borane complexes of Group 6 transition metals were prepared by direct dihydroborane coordination to the metal center. Reaction of [M(CO) 3 (PCy 3 ) 2 ] and two dihydroboranes [DurBH 2 ] and [(Me 3 Si) 2 NBH 2 ] (Dur=2,3,5,6-Me 4 C 6 H) yielded bis(σ)-borane complexes fac-[M(CO) 3 (PCy 3 ){η 2 -(H 2 BR)}] (R=Dur; 1: M=Cr, 2: M=W; R=N(SiMe 3 ) 2 ; 3: M=Cr, 4: M=W). In the case of molybdenum, we have isolated an arene complex (5) with [DurBH 2 ] in which the Dur group acts as a η 6 -bound ligand, and with [(Me 3 Si) 2 NBH 2 ] a similar bis(σ)-borane complex was isolated, cis,trans-[Mo(CO) 2 (PCy 3 ) 2 {η 2 -(H 2 BN(SiMe 3 ) 2 }] (6), with a different pattern of auxiliary ligands. The complexes were investigated by multinuclear NMR spectroscopy, mass spectrometry, X-ray diffraction analysis, and computational methods. Quantum theory of atoms in molecules (QTAIM) calculations demonstrated that the borane complexes may be described as pure bis(σ)-borane complexes rather than elongated or stretched examples given that the calculations do not show the presence of a ring-critical point (RCP) at the ring formed by the interactions of the B-H with metal center., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A series of agostic σ-borane/borate complexes have been synthesized and structurally characterized from simple borane adducts. A room-temperature reaction of [Cp*Mo(CO)3 Me], 1 with Li[BH3 (EPh)] (Cp*=pentamethylcyclopentadienyl, E=S, Se, Te) yielded hydroborate complexes [Cp*Mo(CO)2 (μ-H)BH2 EPh] in good yields. With 2-mercapto-benzothiazole, an N,S-carbene-anchored σ-borate complex [Cp*Mo(CO)2 BH3 (1-benzothiazol-2-ylidene)] (5) was isolated. Further, a transmetalation of the B-agostic ruthenium complex [Cp*Ru(μ-H)BHL2 ] (6, L=C7 H4 NS2 ) with [Mn2 (CO)10 ] affords a new B-agostic complex, [Mn(CO)3 (μ-H)BHL2 ] (7) with the same structural motif in which the central metal is replaced by an isolobal and isoelectronic [Mn(CO)3 ] unit. Natural-bond-orbital analyses of 5-7 indicate significant delocalization of the electron density from the filled σBH orbital to the vacant metal orbital., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A high-yielding synthetic route for the preparation of group 9 metallaboratrane complexes [Cp*MBH(L)2], 1 and 2 (1, M=Rh, 2, M=Ir; L=C7H4NS2) has been developed using [{Cp*MCl2}2] as precursor. This method also permitted the synthesis of an Rh-N,S-heterocyclic carbene complex, [(Cp*Rh)(L2)(1-benzothiazol-2-ylidene)] (3; L=C7H4NS2) in good yield. The reaction of compound 3 with neutral borane reagents led to the isolation of a novel borataallyl complex [Cp*Rh(L)2B{CH2C(CO2Me)}] (4; L=C7H4NS2). Compound 4 features a rare η(3)-interaction between rhodium and the B-C-C unit of a vinylborane moiety. Furthermore, with the objective of generating metallaboratranes of other early and late transition metals through a transmetallation approach, reactions of rhoda- and irida-boratrane complexes with metal carbonyl compounds were carried out. Although the objective of isolating such complexes was not achieved, several interesting mixed-metal complexes [{Cp*Rh}{Re(CO)3}(C7H4NS2)3] (5), [Cp*Rh{Fe2(CO)6}(μ-CO)S] (6), and [Cp*RhBH(L)2W(CO)5] (7; L=C7H4NS2) have been isolated. All of the new compounds have been characterized in solution by mass spectrometry, IR spectroscopy, and (1)H, (11)B, and (13)C NMR spectroscopies, and the structural types of 4-7 have been unequivocally established by crystallographic analysis., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Building upon our earlier results on the synthesis of electron-precise transition-metal-boron complexes, we continue to investigate the reactivity of pentaborane(9) and tetraborane(10) analogues of ruthenium and rhodium towards thiazolyl and oxazolyl ligands. Thus, mild thermolysis of nido-[(Cp*RuH)2B3H7] (1) with 2-mercaptobenzothiazole (2-mbtz) and 2-mercaptobenzoxazole (2-mboz) led to the isolation of Cp*-based (Cp* = η(5)-C5Me5) borate complexes 5 a,b [Cp*RuBH3L] (5 a: L = C7H4NS2; 5 b: L = C7H4NOS)) and agostic complexes 7 a,b [Cp*RuBH2(L)2], (7 a: L = C7H4NS2; 7 b: L = C7H4NOS). In a similar fashion, a rhodium analogue of pentaborane(9), nido-[(Cp*Rh)2B3H7] (2) yielded rhodaboratrane [Cp*RhBH(L)2], 10 (L = C7H4NS2). Interestingly, when the reaction was performed with an excess of 2-mbtz, it led to the formation of the first structurally characterized N,S-heterocyclic rhodium-carbene complex [(Cp*Rh)(L2)(1-benzothiazol-2-ylidene)] (11) (L = C7H4NS2). Furthermore, to evaluate the scope of this new route, we extended this chemistry towards the diruthenium analogue of tetraborane(10), arachno-[(Cp*RuCO)2B2H6] (3), in which the metal center possesses different ancillary ligands., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The synthesis, structural characterization, and reactivity of new bridged borylene complexes are reported. The reaction of [{Cp*CoCl}2] with LiBH4·THF at -70 °C, followed by treatment with [M(CO)3(MeCN)3] (M=W, Mo, and Cr) under mild conditions, yielded heteronuclear triply bridged borylene complexes, [(μ3-BH)(Cp*Co)2(μ-CO)M(CO)5] (1-3; 1: M=W, 2: M=Mo, 3: M=Cr). During the syntheses of complexes 1-3, capped-octahedral cluster [(Cp*Co)2(μ-H)(BH)4{Co(CO)2}] (4) was also isolated in good yield. Complexes 1-3 are isoelectronic and isostructural to [(μ3-BH)(Cp*RuCO)2(μ-CO){Fe(CO)3}] (5) and [(μ3-BH)(Cp*RuCO)2(μ-H)(μ-CO){Mn(CO)3}] (6), with a trigonal-pyramidal geometry in which the μ3-BH ligand occupies the apical vertex. To test the reactivity of these borylene complexes towards bis-phosphine ligands, the room-temperature photolysis of complexes 1-3, 5, 6, and [{(μ3-BH)(Cp*Ru)Fe(CO)3}2(μ-CO)] (7) was carried out. Most of these complexes led to decomposition, although photolysis of complex 7 with [Ph2P(CH2)(n)PPh2] (n=1-3) yielded complexes 9-11, [3,4-(Ph2P(CH2)(n)PPh2)-closo-1,2,3,4-Ru2Fe2(BH)2] (9: n=1, 10: n=2, 11: n=3). Quantum-chemical calculations by using DFT methods were carried out on compounds 1-3 and 9-11 and showed reasonable agreement with the experimentally obtained structural parameters, that is, large HOMO-LUMO gaps, in accordance with the high stabilities of these complexes, and NMR chemical shifts that accurately reflected the experimentally observed resonances. All of the new compounds were characterized in solution by using mass spectrometry, IR spectroscopy, and (1)H, (13)C, and (11)B NMR spectroscopy and their structural types were unequivocally established by crystallographic analysis of complexes 1, 2, 4, 9, and 10., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Room temperature photolysis of a triply-bridged borylene complex, [(μ(3)-BH)(Cp*RuCO)(2)(μ-CO)Fe(CO)(3)] (1 a; Cp* = C(5)Me(5)), in the presence of a series of alkynes, 1,2-diphenylethyne, 1-phenyl-1-propyne, and 2-butyne led to the isolation of unprecedented vinyl-borylene complexes (Z)-[(Cp*RuCO)(2)(μ-CO)B(CR)(CHR')] (2: R, R' = Ph; 3: R = Me, R' = Ph; 4: R, R' = Me). This reaction permits a hydroboration of alkyne through an anti-Markovnikov addition. In stark contrast, in the presence of phenylacetylene, a metallacarborane, closo-[1,2-(Cp*Ru)(2)(μ-CO)(2){Fe(2)(CO)(5)}-4-Ph-4,5-C(2)BH(2)] (5 a), is formed. A plausible mechanism has been proposed for the formation of vinyl-borylene complexes, which is supported by density functional theory (DFT) methods. Furthermore, the calculated (11)B NMR chemical shifts accurately reflect the experimentally measured shifts. All the new compounds have been characterized in solution by mass spectrometry and IR, (1)H, (11)B, and (13)C NMR spectroscopies and the structural types were unequivocally established by crystallographic analysis of 2, 5 a, and 5 b., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The reaction of [Cp(n)MCl(4-x)] (M=V: n=2, x=2; M=Nb: n=1, x=0; Cp=η(5)-C(5) H(5)) with LiBH(4)⋅THF followed by thermolysis in the presence of dichalcogenide ligands E(2)R(2) (E=S, Te; R=2,6-(tBu)(2)-C(6)H(2)OH, Ph) and 2-mercaptobenzothiazole (C(7)H(5)NS(2)) yielded dimetallaheteroboranes [{CpV(μ-TePh)}(2)(μ(3) -Te)BH⋅thf] (1), [(CpV)(2)(BH(3)S)(2)] (2), [(CpNb)(2)B(4)H(10)S] (3), [(CpNb)(2)B(4)H(11)S(tBu)(2)C(6)H(2)OH] (4), and [(CpNb)(2)B(4)H(11)TePh] (5). In cluster 1, the V(2)BTe atoms define a tetrahedral framework in which the boron atom is linked to a THF molecule. Compound 2 can be described as a dimetallathiaborane that is built from two edge-fused V(2)BS tetrahedron clusters. Cluster 3 can be considered as an edge-fused cluster in which a trigonal-bipyramidal unit (Nb(2)B(2)S) has been fused with a tetrahedral core (Nb(2)B(2)) by means of a common Nb(2) edge. In addition, thermolysis of an in-situ-generated intermediate that was produced from the reaction of [Cp(2)VCl(2)] and LiBH(4)⋅THF with excess BH(3)⋅THF yielded oxavanadaborane [(CpV)(2)B(3)H(8)(μ(3)-OEt)] (6) and divanadaborane cluster [(CpV)(2)B(5)H(11)] (7). Cluster 7 exhibits a nido geometry with C(2v) symmetry and it is isostructural with [(Cp*M)(2)B(5)H(9+n)] (M=Cr, Mo, and W, n=0; M=Ta, n=2; Cp*=η(5)-C(5)Me(5)). All of these new compounds have been characterized by (1)H NMR, (11)B NMR, and (13)C NMR spectroscopy and elemental analysis and the structural types were established unequivocally by crystallographic analysis of compounds 1-4, 6, and 7., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)