M-Commerce
DOI: 10.4018/9781591403159.ch008
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Cited by 8 publications
(8 citation statements)
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“…The very low 12 C/ 13 C ratios (0.3-3) observed in novae are due to the 12 C(p, γ) 13 N(β + ) 13 C chain reaction during burning of the accreted hydrogen (José & Hernanz, 2007). These predictions of very low 12 C/ 13 C ratios are consistent with limits on the 12 C/ 13 C ratio estimated from fitting of 13 CO and 12 CO bands in the infrared spectra of several nova ejecta (Banerjee & Ashok, 2012;Banerjee et al 2016;Evans & Rawlings, 2008). Based on the composition of the WD core, we distinguish two types of novae: CO novae, for initial masses of the primary star below ~8 M , which undergo hydrogen and helium burning, leaving a carbonand oxygen-rich WD core; and ONe novae for slightly more massive stars (8-10 M ) which, in addition, undergo carbon burning, leaving an oxygen-and neon-rich WD core (José, 2016;José et al 2004).…”
Section: Lap-149: Extremely 13 C-rich Presolar Graphite From a Low-masupporting
confidence: 78%
“…The very low 12 C/ 13 C ratios (0.3-3) observed in novae are due to the 12 C(p, γ) 13 N(β + ) 13 C chain reaction during burning of the accreted hydrogen (José & Hernanz, 2007). These predictions of very low 12 C/ 13 C ratios are consistent with limits on the 12 C/ 13 C ratio estimated from fitting of 13 CO and 12 CO bands in the infrared spectra of several nova ejecta (Banerjee & Ashok, 2012;Banerjee et al 2016;Evans & Rawlings, 2008). Based on the composition of the WD core, we distinguish two types of novae: CO novae, for initial masses of the primary star below ~8 M , which undergo hydrogen and helium burning, leaving a carbonand oxygen-rich WD core; and ONe novae for slightly more massive stars (8-10 M ) which, in addition, undergo carbon burning, leaving an oxygen-and neon-rich WD core (José, 2016;José et al 2004).…”
Section: Lap-149: Extremely 13 C-rich Presolar Graphite From a Low-masupporting
confidence: 78%
“…[15] However,r elated umpolung transformations utilizing open-shell acyl radicals are still underdeveloped. [16] Until very recently,M elchiorre [16e] and Yu [16f] disclosed two ground-breaking work in which amine-catalyzed asymmetric additions to enals by acyl radicals were accomplished independently by combining with direct photoexcitation and photoredox catalysis.E ncouraged by our above success,w e planned to apply the same DCo5 complex to the visible-lightinduced asymmetric conjugated addition of enones by acyl radicals in the absence of additional photocatalyst. As highlighted in Figure 4, as eries of aryl-containing acyl radicals generated from corresponding HEs 8 can participate in this reaction, affording chiral 1,4-dicarbonyl products in good yields and enantioselectivities (9a-9g:94-> 99 %yields and up to 94:6 e.r.).…”
Section: Angewandte Chemiementioning
confidence: 99%
“…In the literature, there are extremely insightful articles that offer an overview of the coherent oxide heterostructures from experimental and computational perspectives. [1][2][3]8,15,18,20,31,[47][48][49] Predominantly, there are several DFT-based computational studies in the literature that address what are presumably semi-coherent oxide interfaces in reality, but constrain them to be coherent. [32,[50][51][52][53][54][55][56] Forcing the two oxides to be coherent allows the implementation of smaller supercells to mimic the oxide heterostructures, which are tractable by DFT calculations.…”
Section: Introductionmentioning
confidence: 99%