Abstract
The thermolysis of arachno-1 [(Cp*Ru)2(B3H8)(CS2H)] in the presence of tellurium powder yielded a series of ruthenium trithia-borinane complexes: [(Cp*Ru)2(η1-S)(η1-CS){(CH2)2S3BH}] 2, [(Cp*Ru)2(η1-S)(η1-CS){(CH2)2S3B(SMe)}] 3, and [(Cp*Ru)2(η1-S)(η1-CS){(CH2)2S3BH}] 4. Compounds 2–4 were considered as ruthenium trithia-borinane complexes, where the central six-membered ring {C2BS3} adopted a boat conformation. Compounds 2–4 were similar to our recently reported ruthenium diborinane complex [(Cp*Ru){(η2-SCHS)CH2S2(BH2)2}]. Unlike diborinane, where the central six-membered ring {CB2S3} adopted a chair conformation, compounds 2–4 adopted a boat conformation. In an attempt to convert arachno-1 into a closo or nido cluster, we pyrolyzed it in toluene. Interestingly, the reaction led to the isolation of a capped butterfly cluster, [(Cp*Ru)2(B3H5)(CS2H2)] 5. All the compounds were characterized by 1H, 11B{1H}, and 13C{1H} NMR spectroscopy and mass spectrometry. The molecular structures of complexes 2, 3, and 5 were also determined by single-crystal X-ray diffraction analysis.
Highlights
The mutually synergistic interactions between metals and organic ligands often generate compounds of fundamental and practical importance [1,2,3,4,5,6]
The present work describes the synthesis of various borinane complexes of a group-8 heavier transition metal from a dithioformato stabilized arachno-diruthenium pentaborane cluster
Adopt a boat confirmation, which is in contrast to our previously reported trithia-diborinane complexes of ruthenium, [(Cp*Ru){(η2 -SCHS)CH2 S2 (BH2 )2 }], which adopt a chair conformation
Summary
The mutually synergistic interactions between metals and organic ligands often generate compounds of fundamental and practical importance [1,2,3,4,5,6]. There is still little understanding of how a transition metal can be used to vary the chemistry of metallaborane compounds In this regard, our group was actively involved in the synthesis of various electron-precise transition metal–boron complexes such as σ-borane [26,27,28,29,30,31], boryl [32,33], triply-bridged trimetallic borylene [34,35,36,37,38], diborane [39], B-agostic [26,27,40,41,42], and metallaboratrane [26,27,43,44] complexes using of different synthetic precursors. The chemistry of transition-metal complexes with main group elements, with chalcogen ligands, are of substantial importance. The homo- and heterometallic sulfido complexes with a wide range of substrates are well-documented in the literature [50,51,52,53]
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