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Moreover, the support of above approach by use of Positron Annihilation Lifetime Spectroscopy (PALS) could provide the information related to the free volume holes changes associated with structural bonding transformation.
In addition, sp2 to sp3 bonding transformation through the quantification of the deconvolution of the XPS C (1s) envelope along with electronic damage as deduced from the gradual disappearance of the π − π* transition in graphene, as a function of irradiation energy, was found.
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1-dimensional phase lag modeling technique was used to estimate the time required for complete bond transformation to intermetallics.
First, the elastic, piezoelectric and piezomagnetic coefficients in the considered ordinate system are obtained by Bond transformation from that in the crystal axis ordinate system.
Nitrogen-doped reduced graphene oxide (N-rGO) has been synthesized using a simple, efficient method combining instant thermal exfoliation and covalent bond transformation from a melamine-graphene oxide mixture.
The possibility of direct formation of a new carbon carbon bond by C H bond transformation is a highly attractive strategy in covalent synthesis, owing to the ubiquitous nature of C H bonds in organic substances and the high atom economy of the process.
Direct studies of diradicals, the molecular species hypothesized to be archetypal of chemical bond transformations in many classes of reactions, have been made using femtosecond laser techniques with mass spectrometry in a molecular beam.
A transition of bending stiffness in two specific dehydrogenation-free DNTs occurring at critical curvatures is detected as a consequence of local bond transformations.
Multiple pathways leading to the formation of the C28 sterol ergosterol vary according to the sequence of double bond transformations.
Apparently, unlike higher plants, the final double bond transformations (Δ7 > Δ5,7 > Δ5) to complete the synthesis to the end-product, i.e., Δ5, do not occur in the rust fungi, resulting in Δ7 and Δ7,24(28) sterols.
Most fungal sterols are distinguished by the methylation of lanosterol at C-24, and thereafter follow the same series of demethylations at C-4 and C-14 and double bond transformations as in cholest-5-enol (cholesterol) biosynthesis that lead to C28 sterols common in most fungi.
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