
@article {205,
	title = {Synthesis of 1,2,4,5-oxadiazaboroles by three-component condensations of hydroxylamines, nitriles, and diarylborinic acids},
	journal = {Canadian Journal of Chemistry},
	year = {2023},
	month = {2023/02/23},
	abstract = {A method for the synthesis of substituted 1,2,4,5-oxadiazaboroles is described, in which hydroxylamines, nitriles, and diarylborinic acids engage in a three-component condensation reaction. The protocol provides access to a substitution pattern that is not readily available through other methods?namely, 2,3-disubstitution, with a tetracoordinate boron center. Structures of representative members of this class of heterocycles were determined by single crystal X-ray diffraction analysis.A method for the synthesis of substituted 1,2,4,5-oxadiazaboroles is described, in which hydroxylamines, nitriles, and diarylborinic acids engage in a three-component condensation reaction. The protocol provides access to a substitution pattern that is not readily available through other methods?namely, 2,3-disubstitution, with a tetracoordinate boron center. Structures of representative members of this class of heterocycles were determined by single crystal X-ray diffraction analysis.},
	isbn = {0008-4042},
	url = {https://doi.org/10.1139/cjc-2022-0200},
	author = {Ge, Zhenlu and Lough, Alan J. and Taylor, Mark S.}
}
@article {98,
	title = {Halogen bonding and pi,pi interactions in the solid-state structure of a butadiynylene-linked bis(iodoperfluoroarene)},
	journal = {CrystEngComm},
	volume = {15},
	year = {2013},
	month = {2013},
	pages = {3097 - 3101},
	abstract = {<p>The solid-state structures of a butadiynylene-linked bidentate halogen bond donor, both as a single component and as a co-crystal with tetra-n-butylammonium iodide, are discussed. Solution-phase binding data indicate that this donor, which possesses only a single degree of conformational freedom, interacts with halides in a 1 : 1 stoichiometry through a convergent binding mode. In contrast, it forms a zigzag-type chain with iodide in the solid state. The X-ray crystallographic data enable detailed studies of the changes in molecular structure and supramolecular organization that accompany the formation of a halogen-bonded network.</p>},
	url = {http://dx.doi.org/10.1039/C2CE26751A},
	author = {Walter, Sebastian M. and Sarwar, Mohammed G. and Chudzinski, Michael G. and Herdtweck, Eberhardt and Lough, Alan J. and Huber, Stefan M. and Taylor, Mark S.}
}
@article {85,
	title = {N,N'-Diarylsquaramides: General, High-Yielding Synthesis and Applications in Colorimetric Anion Sensing},
	journal = {The Journal of Organic Chemistry},
	volume = {75},
	year = {2010},
	month = {2010/06/18},
	pages = {3983 - 3992},
	isbn = {0022-3263},
	url = {http://dx.doi.org/10.1021/jo100104g},
	author = {Rostami, Ali and Colin, Alexis and Li, Xiao Yu and Chudzinski, Michael G. and Lough, Alan J. and Taylor, Mark S.}
}
