Formation of gallaoxetanes: C-O activation of 1,2-epoxybutane by ground-state Ga atoms.

(69/71)Ga atoms were reacted with 1,2-epoxybutane and its isotopomers, 1,2-epoxybutane-1,1-d(2) (CH(3)CH(2)CHOCD(2)) and 1,2-epoxybutane-2-d(1) (CH(3)CH(2)CDOCH(2)), under matrix-isolation conditions. The novel gallaoxetanes CH(3)CH(2)CHCH(2)GaO and CH(3)CH(2)CHCH(2)OGa, resulting from the insertion of the metal atom in the C(1)-O and C(2)-O bonds, respectively, of the 1,2-epoxybutane, were detected by EPR spectroscopy. The Ga and H hyperfine interaction (hfi) values of the gallaoxetanes, calculated using a DFT method, were used to help assign the EPR spectra.

Placental pathology and clinical outcomes in a cohort of infants admitted to a neonatal intensive care unit.

Background: Placental pathology predicts persistent neurological impairment, even in normally grown infants. However, few studies have linked placental pathology with neonatal outcomes in a large population.

Methods: We matched the clinical outcomes of a cohort of neonates admitted to a neonatal intensive care unit (NICU) with placental pathology, where available, and examined (by multivariable logistic regression) the relationship between placental pathologies and these outcomes.

An EPR study of the C-O bond activation of 1,2-epoxybutane by ground-state Al atoms.

Group 13 metal atoms react with ethers under matrix isolation conditions to give a number of interesting products. This work has been extended to include the reaction of Al atoms with 1,2-epoxybutane (CH(3)CH(2)H(2)) and its isotopomers, 1,2-epoxybutane-1,1-d(2) (CH(3)CH(2)D(2)) and 1,2-epoxybutane-2-d(1) (CH(3)CH(2)H(2)). The paramagnetic species generated in the reaction have been studied by electron paramagnetic resonance (EPR) spectroscopy.