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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=160079"><dc:title>Towards structurally versatile mesoionic N-heterocyclic olefin ligands and their coordination to palladium, gold, and boron hydride</dc:title><dc:creator>Ževart,	Tisa	(Avtor)
	</dc:creator><dc:creator>Pinter,	Balazs	(Avtor)
	</dc:creator><dc:creator>Lozinšek,	Matic	(Avtor)
	</dc:creator><dc:creator>Urankar,	Damijana	(Avtor)
	</dc:creator><dc:creator>Jansen-van Vuuren,	Ross D.	(Avtor)
	</dc:creator><dc:creator>Košmrlj,	Janez	(Avtor)
	</dc:creator><dc:subject>coordination</dc:subject><dc:subject>boron hydride</dc:subject><dc:description>We have developed an efficient and versatile approach for the synthesis of a family of 1,2,3-triazole-based mesoionic N-heterocyclic olefin (mNHO) ligands and investigated their coordination to palladium, gold, and boron hydride experimentally and computationally. We reacted mNHOs obtained through deprotonation of the corresponding methylated and ethylated 1,3,4-triaryl-1,2,3-triazolium salts with [Pd(allyl)Cl]$_2$ to give the corresponding [Pd(η$^3$-allyl)Cl(mNHO)] coordination complexes. $^{13}$C NMR data revealed the strong σ-donor character of the mNHO ligands, consistent with the calculated bond orders and atom-condensed charges. Furthermore, we also synthesized [AuCl(mNHO)] and a BH$_3$–mNHO adduct by reacting the triazolium salts with AuCl(SMe$_2$) and BH$_3$·THF, respectively. The BH$_3$–mNHO adduct was tested in the reduction of select aldehydes and ketones to alcohols.</dc:description><dc:date>2024</dc:date><dc:date>2024-08-16 11:46:26</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>160079</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
