@phdthesis{Ye2012,
  author    = {Ye, Qing},
  title     = {Synthesis and Investigation of Borylene Complexes: from Borylene Transfer to Borylene Catenation},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-71443},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2012},
  abstract  = {Im Rahmen dieser Arbeit wurde das Spektrum des Borylentransfers ausgeweitet, indem {\"U}bergangsmetall Alkinylkomplexe und Metall-Kohlenstoff-Doppelbindungen als Borylen-Akzeptoren eingeschlossen wurden. Neben der Salzeliminierung, Halogenidabstraktion und Dehydrierung, wurde eine neuartige Syntheseroute zu terminalen Borylenkomplexen durch Salz- und Silylhalogenideliminierung etabliert. Mithilfe dieser Strategie gelang die Darstellung von [(OC)3(Me3P)Fe=BDur], ein seltenes Beispiel f{\"u}r einen neutralen Arylborylenkomplex. Im Speziellen hat diese Verbindung ein großes Anwendungspotenzial f{\"u}r Metathesereaktionen und die Funktionalisierung von polycyclischen aromatischen Kohlenwasserstoffen, wie z. B. Naphthalin, gezeigt. Außerdem konnte ein Eisen-Bis(borylen)-Komplex [(OC)3Fe(BDur){BN(SiMe3)2}] durch einen Phosphan-Borylen-Austausch dargestellt werden. Ausgehend von diesem Komplex gelang die Darstellung von 1,4-Diboracyclohexadien bzw. des ersten 1,4-Dibora-1,3-Butadien-Komplexes, wodurch eine neue Art von Borylentransfer etabliert werden konnte. H{\"o}chst interessant ist es, dass der Transfer von weiteren Borylen-Einheiten in die Koordinationssph{\"a}re des Eisenatoms zu einer kontrollierten Borylen-Verkettung gef{\"u}hrt hat.},
  subject      = {Borylene},
  language  = {en}
}
@unpublished{SchmidtFantuzziArrowsmithetal.2020,
  author    = {Schmidt, Uwe and Fantuzzi, Felipe and Arrowsmith, Merle and Hermann, Alexander and Prieschl, Dominic and Rempel, Anna and Engels, Bernd and Braunschweig, Holger},
  title     = {Tuneable reduction of cymantrenylboranes to diborenes or borylene-derived boratafulvenes},
  series = {Chemical Communications},
  journal   = {Chemical Communications},
  doi       = {10.1039/D0CC06398C},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-222149},
  year      = {2020},
  abstract  = {Whereas the reduction of N-heterocyclic carbene (NHC)-stabilised cymantrenyldibromoboranes, (NHC)BBr\(_2\)Cym, in benzene results in formation of the corresponding diborenes (NHC)\(_2\)B\(_2\)Cym\(_2\), a change of solvent to THF yields a borylene of the form (NHC)\(_2\)BCym, stabilised through its boratafulvene resonance form.},
  language  = {en}
}
@article{LiuLegareSeufertetal.2020,
  author    = {Liu, Siyuan and L{\´e}gar{\´e}, Marc-Andr{\´e} and Seufert, Jens and Prieschl, Dominic and Rempel, Anna and Englert, Lukas and Dellermann, Theresa and Paprocki, Valerie and Stoy, Andreas and Braunschweig, Holger},
  title     = {2,2′-Bipyridyl as a Redox-Active Borylene Abstraction Agent},
  series = {Inorganic Chemistry},
  volume    = {59},
  journal   = {Inorganic Chemistry},
  number    = {15},
  doi       = {10.1021/acs.inorgchem.0c01383},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-215595},
  pages     = {10866-10873},
  year      = {2020},
  abstract  = {2,2′-Bipyridyl is shown to spontaneously abstract a borylene fragment (R-B:) from various hypovalent boron compounds. This process is a redox reaction in which the bipyridine is reduced and becomes a dianionic substituent bound to boron through its two nitrogen atoms. Various transition metal-borylene complexes and diboranes, as a well as a diborene, take part in this reaction. In the latter case, our results show an intriguing example of the homolytic cleavage of a B═B double bond.},
  language  = {en}
}
@phdthesis{Liu2020,
  author    = {Liu, Siyuan},
  title     = {New Avenues in the Reactivity of Borylene Complexes},
  doi       = {10.25972/OPUS-18430},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-184302},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2020},
  abstract  = {The thesis is mainly about the reactivities of borylene complexes. Including the investigation of the reaction of base stabilized terminal borylene with elemental chalcogens. On the other hand the are also the reactivity of borylene with bipyridine species is also studies. A C-H activation of the Cp2WH2 using borylene is also discovered. Finally the reaction of a borylene with Lewis acids such as GaCl3 and InBr3 is also studied.},
  subject      = {Borylene},
  language  = {en}
}
@phdthesis{Hagspiel2022,
  author    = {Hagspiel, Stephan Alexander},
  title     = {Synthesis and Reactivity of Pseudohalide-substituted Boranes and Borylenes},
  doi       = {10.25972/OPUS-24945},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-249459},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2022},
  abstract  = {This work involves the synthesis and reactivity of pseudohalide-substituted boranes and borylenes. A series of compounds of the type (CAAC)BR2Y (CAAC = cyclic alkyl(amino)carbene; R = H, Br; Y = CN, NCS, PCO) were prepared first. The two-electron reduction of (CAAC)BBr2Y (Y = CN, NCS) in the presence of a second Lewis base L (L = N-heterocyclic carbene) resulted in the formation of the corresponding doubly Lewis base-stabilized pseudohaloborylenes (CAAC)(L)BY. These borylenes show versatile reactivity patterns, including their oxidation to the corresponding radical cations, coordination via the respective pseudohalide substituent to group 6 metal carbonyl complexes, as well as a boron-centered protonation with Br{\o}nsted acids to boronium cations. Reduction of (CAAC)BBr2(NCS) in the absence of a second donor ligand, led to the formation of boron-doped thiazolothiazoles via reductive dimerization of two isothiocyanatoborylenes. These B,N,S-heterocycles possess a low degree of aromaticity as well as interesting photophysical properties and can furthermore be protonated as well as hydroborated. Additionally, CAAC adducts of the parent boraphosphaketene (CAAC)BH2(PCO) could be prepared, which readily reacted with boroles [Ph4BR'] (R' = aryl) via decarbonylation in a ring expansion reaction. The obtained 1,2-phosphaborinines represent B,P-isosteres of benzene and consequently could be coordinated to metal carbonyl complexes of the chromium triade via η6-coordination, resulting in new half-sandwich complexes thereof.},
  subject      = {Borylene},
  language  = {en}
}