1998
DOI: 10.1070/rc1998v067n12abeh000434
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2,3,4,5-Tetrahydropyridine (Δ1-piperideine) and its derivatives. Synthesis and chemical properties

Abstract: We study the influence of the tetragonalization occurring during the martensitic phase transition on the exchange interactions in Ni 2 MnGa Heusler alloy using first-principles calculations in conjunction with the frozen-magnon approximation. We show that the tetragonalization alters only the exchange constants characterizing the Mn-Mn interactions. Calculated Curie temperatures within the random-phase approximation are found to agree with experimental data. Moreover, we study the temperature dependence of the… Show more

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Cited by 6 publications
(4 citation statements)
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“…The aromatic vitamin B3 derivatives 10-13 have enhanced thermodynamic stability [94] compared to the non-aromatized quinolinic acid derivatives 6-9, whose piperideine ring is highly reactive. [95] Therefore, the final non-aromatized quinolinic acid derivative 9 might be less stable and more likely to decompose to other organics than vitamin B3 13. Some planetesimals, which have the right balance of a big enough size ≳ 10 km and late enough time of formation ≳ 2.5 Myr, can maintain aqueous conditions in their porous interiors for hundreds of thousands to millions of years.…”
Section: Reaction Pathwaymentioning
confidence: 99%
“…The aromatic vitamin B3 derivatives 10-13 have enhanced thermodynamic stability [94] compared to the non-aromatized quinolinic acid derivatives 6-9, whose piperideine ring is highly reactive. [95] Therefore, the final non-aromatized quinolinic acid derivative 9 might be less stable and more likely to decompose to other organics than vitamin B3 13. Some planetesimals, which have the right balance of a big enough size ≳ 10 km and late enough time of formation ≳ 2.5 Myr, can maintain aqueous conditions in their porous interiors for hundreds of thousands to millions of years.…”
Section: Reaction Pathwaymentioning
confidence: 99%
“…In the potential absence of free oxygen in carbonaceous planetesimals, the synthesis of vitamin B 3 in its aromatized form might even be favored over quinolinic acid (following Scheme 1). The aromatic vitamin B 3 derivatives 10–13 have enhanced thermodynamic stability [94] compared to the non‐aromatized quinolinic acid derivatives 6–9 , whose piperideine ring is highly reactive [95] . Therefore, the final non‐aromatized quinolinic acid derivative 9 might be less stable and more likely to decompose to other organics than vitamin B 3 13 .…”
Section: Resultsmentioning
confidence: 99%
“…The aromatic vitamin B 3 derivatives 10-13 have enhanced thermodynamic stability [94] compared to the nonaromatized quinolinic acid derivatives 6-9, whose piperideine ring is highly reactive. [95] Therefore, the final non-aromatized quinolinic acid derivative 9 might be less stable and more likely to decompose to other organics than vitamin B 3 13. Some planetesimals, which have the right balance of a big enough size 10 km and late enough time of formation 2:5 Myr, can maintain aqueous conditions in their porous interiors for hundreds of thousands to millions of years.…”
Section: Reaction Pathwaymentioning
confidence: 99%
“…Chrysin (7a) and Δ 1 -piperideine (3,4,5,6-tetrahydropyridine, 8a) [8] were used as representative substrates in our initial survey of reaction conditions (Table 1). In DMF, a dipolar aprotic solvent, at 80°C, the conversion was low and the reaction gave an equimolar mixture of separable C-6/C-8 regioisomers (Table 1, Entry 1).…”
Section: Resultsmentioning
confidence: 99%