David B. McConville
University of Akron
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Featured researches published by David B. McConville.
Tetrahedron Letters | 1998
Manisha Chakraborty; David B. McConville; Takeshi Saito; Huihan Meng; Peter L. Rinaldi; Claire A. Tessier; Wiley J. Youngs
Abstract A new palladium-copper catalyzed intramolecular acetylene-zipper type bicyclization between alkyne and hydroxy functionality of an alkynyl hydroquinone has been observed to give a highly conjugated ring system.
Journal of Chemical Crystallography | 1995
Gerald F. Koser; David B. McConville; Ghada A. Rabah; Wiley J. Youngs
AbstractThe title compound,6, a novel 1∶1 complex of 1-chloro-1,2-benziodoxolin-3(1H)-one (5) andtetra-n-butylammonium chloride, was prepared from tetra-n-butylammoniumo-iodoxybenzoate (7) and acetyl chloride. A single crystal of6 was subjected to X-ray analysis: triclinic, space group
Inorganic Chemistry | 1997
Subodh Kanti Dutta; David B. McConville; Wiley J. Youngs; Muktimoy Chaudhury
Inorganic Chemistry | 1996
Paul R. Klich; Andrew T. Daniher; Paul R. Challen; David B. McConville; Wiley J. Youngs
P\bar 1;
Journal of the American Chemical Society | 1993
Anthony J. Pearson; Ping Y. Zhu; Wiley J. Youngs; John D. Bradshaw; David B. McConville
Macromolecules | 1997
Kathy C. Chuang; James D. Kinder; Diana L. Hull; David B. McConville; Wiley J. Youngs
a=10.239(2),b=11.518(2),c=11.523(3)Å; α=73.20(2); β=87.85(2), γ=87.72(2)°; R1=0.0326. The most notable structural feature of crystalline6 is the existence of a “secondary” bond [I· ·Cl(2), 2.943(1)Å] between the chloride ion and the iodine atom of the chlorobenziodoxolinone moiety. Further coordination at iodine includes three primary bonds: I−C [2.115(4) Å], I−O [2.145(3) Å], I−Cl(1) [2.454(1) Å]. The entire 1-chlorobenziodoxolinone-chloride sub-structure is planar and exhibits iodine-centered bond angles of 78.8(1)° [C−I−O], 92.0(1)° [C−I−Cl(1)], 97.6(1)° [Cl(2)−I−O] and 91.6(1)° [Cl(2)−I−Cl(1)]. The unit cell of6 contains two loosely packed formula units. The chlorobenziodoxolinone-chloride sub-structures occupy a common plane and exhibit a centrosymmetric relationship, while the tetra-n-butylammonium ions are situated one above and one below the plane. Bonding at the iodine atom in6 is more consistent with a 10-I-3 species electrostatically associated with the chloride ion than a 12-I-4 species such as the tetrachloroiodate ion.
Organometallics | 1994
Anthony J. Pearson; Kieyoung Chang; David B. McConville; Wiley J. Youngs
Organometallics | 1997
Da-Ming Zhang; David B. McConville; Claire A. Tessier; Wiley J. Youngs
Journal of Organic Chemistry | 1994
Philip Garner; Philip B. Cox; Stephen J. Klippenstein; Wiley J. Youngs; David B. McConville
Organometallics | 1997
Li Guo; John D. Bradshaw; David B. McConville; Claire A. Tessier; Wiley J. Youngs