Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine)

Stephanie Jones; José M. Vargas; Steven Pellizzeri; Charles J. O’Connor; Jon Zubieta

doi:10.1016/J.ICA.2012.10.023

Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine)

Stephanie Jones
, José M. Vargas
, Steven Pellizzeri
, Charles J. O’Connor
, Jon Zubieta

Syracuse University
University of New Orleans

Producción científica › revisión exhaustiva

Idioma original	American English
Publicación	Inorganica Chimica Acta
Volumen	395
DOI	https://doi.org/10.1016/J.ICA.2012.10.023
Estado	Published - ene 30 2013
Publicado de forma externa	Sí

Disciplines

Inorganic Chemistry
Other Earth Sciences

Acceder al documento

10.1016/J.ICA.2012.10.023Licencia: Unspecified

Otros archivos y enlaces

https://experts.syr.edu/en/publications/solid-state-coordination-chemistry-structural-consequences-of-var

Citar esto

Jones, S., Vargas, J. M., Pellizzeri, S., O’Connor, C. J., & Zubieta, J. (2013). Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine). Inorganica Chimica Acta, 395. https://doi.org/10.1016/J.ICA.2012.10.023

Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine). / Jones, Stephanie; Vargas, José M.; Pellizzeri, Steven et al.
En: Inorganica Chimica Acta, Vol. 395, 30.01.2013.

Producción científica › revisión exhaustiva

Jones, S, Vargas, JM, Pellizzeri, S, O’Connor, CJ & Zubieta, J 2013, 'Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine)', Inorganica Chimica Acta, vol. 395. https://doi.org/10.1016/J.ICA.2012.10.023

Jones S, Vargas JM, Pellizzeri S, O’Connor CJ, Zubieta J. Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine). Inorganica Chimica Acta. 2013 ene 30;395. doi: 10.1016/J.ICA.2012.10.023

Jones, Stephanie ; Vargas, José M. ; Pellizzeri, Steven et al. / Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine). En: Inorganica Chimica Acta. 2013 ; Vol. 395.

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title = "Solid state coordination chemistry: Structural consequences of varying diphosphonate tether length and fluoride incorporation in the copper–bisterpy/oxomolybdenum/organodiphosphonate system (bisterpy = 2,2′:4′,4″:2″,2″′-quarterpyridyl-6′,6″-di-2-pyridine)",

author = "Stephanie Jones and Vargas, \{Jos{\'e} M.\} and Steven Pellizzeri and O{\textquoteright}Connor, \{Charles J.\} and Jon Zubieta",

note = "The hydrothermal reactions of Cu(C 2H 3O 2) 2·H 2O, MoO 3, 2,2':4',4″:2″,2'″-quarterpyridyl-6',6″-di-2-pyridine (bisterpy), and organodiphosphonate ligands of varying carbon chain length in the presence of HF yield a series of novel organic-inorganic hybrid materials of the oxomolybdenum-organophosphonate family. All compounds of the study were characterized by elemental analysis, IR spectroscopy, TGA, magnetic susceptibility and single crystal X-ray diffraction.",

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