Dergiler / Organic Communications / 2018 / Cilt: 11 - Sayı: 1

Cycloaddition reactions of silacyclopropylidenoids to ethylene

Sayfa
46–52
DOI
—
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Additionally, the findings show that the silacyclopropylidene addition to ethylene is determined to be exergonic in both gas and THF phases by ΔG = – 42.6 kJ/mol and –39.3 kJ/mol, respectively.

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Amaç & Hipotez:The cycloaddition reactions of silacyclopropylidenoids (C2H4SiXLi, X = F, Cl, Br) to ethylene have been investigated separately to gain insights into halogen and solvation effects on the energetic of the proposed reactions at the B3LYP/6–311+G(d,p) level of theory.
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Temel Bulgular & Veri:The required initial energy barriers for the conversion of silacyclopropylidenoids to silaspiropentanes are determined to be ΔG = 77.4 kJ/mol, 9.6 kJ/mol, and 9.2 kJ/mol for F, Cl, and Br, respectively.
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Sonuç & Katkı:Additionally, the findings show that the silacyclopropylidene addition to ethylene is determined to be exergonic in both gas and THF phases by ΔG = – 42.6 kJ/mol and –39.3 kJ/mol, respectively.
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

The cycloaddition reactions of silacyclopropylidenoids (C2H4SiXLi, X = F, Cl, Br) to ethylene have been investigated separately to gain insights into halogen and solvation effects on the energetic of the proposed reactions at the B3LYP/6–311+G(d,p) level of theory. The calculations reveal that the addition of silacyclopropylidenoids to ethylene occurs via stepwise mechanisms. The required initial energy barriers for the conversion of silacyclopropylidenoids to silaspiropentanes are determined to be ΔG = 77.4 kJ/mol, 9.6 kJ/mol, and 9.2 kJ/mol for F, Cl, and Br, respectively. Furthermore, the gas phase calculations show that the reactions are not spontaneous at room temperature, whereas those of THF solvated models indicate that the formations of silaspiropentanes are spontaneous in the cases of X = Br and Cl. Additionally, the findings show that the silacyclopropylidene addition to ethylene is determined to be exergonic in both gas and THF phases by ΔG = – 42.6 kJ/mol and –39.3 kJ/mol, respectively.

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Bu Makaleye Atıf Yap

YILDIZ, C. B., AZİZOĞLU, A. (2018). Cycloaddition reactions of silacyclopropylidenoids to ethylene. Organic Communications, Cilt: 11 - Sayı: 1, 46–52. https://ajindex.com/articles/288481

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Kaynakça (14)

  1. Mieusset, J. L.; Brinker, U. H. On the existence of uncharged molecules with a pyramidally coordinated carbon: the cases of pentacyclo[4.3.0.02,9.03,8.07,9]non-4-ene and heptacyclo- [7.6.0.01,5.05,15.06,14.010,14.010,15]pentadecane. J. Org. Chem. 2005, 70, 10572-10575
  2. Averina, E. B.; Sedenkova, K. N.; Borisov, I. S.; Grishin, Y. K.; Kuznetzova, T. S.; Zefirov, N. S. Unusual methylation reaction of gem-bromofluorospiropentanes with methyllithium. Tetrahedron 2009, 65, 5693-5701
  3. Kilbas, B.; Azizoglu, A.; Balci, M. Endo- and exo-configured cyclopropylidenes incorporated into the norbornadiene skeleton: generation, rearrangement to allenes, and the effect of remote substituents on carbene stability. J. Org. Chem. 2009, 74, 7075-7083
  4. Escudie, J.; Ranaivonjatovo, H.; Bouslikhane, M.; Harouch, Y. E.; Baiget, L.; Nemes, G. C. Phosphasila-, phosphagerma-, and phosphaarsaallenes P= C= E (E= Si, Ge, As) and arsa- and diarsaallenes As= C= E"(E"= C, As). Russ. Chem. Bull. Int. Ed. 2004, 53, 1020-1033
  5. Escudie, J.; Ranaivonjatovo, H. Group 14 and 15 heteroallenes E=C=C and E=C=E‘. Organomet. 2007, 26, 1542-1559
  6. Gaspar, P.; West, R. The Chemistry of Organic Silicon Compounds, Wiley, New York, 1998
  7. Lee, V. Y.; Sekiguchi, A. Novel organometallic reagents: geminal dianionic derivatives of the heavy group 14 elements. Inorg. Chem. 2011, 50, 12303-12314
  8. Clark, T.; Schleyer, P. v. R. The isomeric structures of SiH2LiF. J. Organomet. Chem. 1980, 191, 347- 353
  9. Feng, D. C.; Feng, S. Y.; Deng, C. H. Theoretical study on the addition reaction of silylenoid H2SiLiF and ethylene. Chem. J. Chin. Univ. 1996, 17, 1108-1111
  10. Zhang, M.; Li, W.; Li, O.; Cheng, J. A new exploration of the addition reaction of the silylenoid H2SiLiF with ethylene. J. Mol. Model. 2015, 21, 202–207
  11. Tamao, K.; Kawachi, A. The chemistry of silylenoids: preparation and reactivity of (alkoxysilyl)lithium compounds. Angew. Chem. Int. Edit. 1995, 34, 818-820
  12. Molev, G.; Bravo–Zhivotovakii, D.; Karni, M.; Tumanskii, B.; Botoshansky, M.; Apeloig, Y. Synthesis, molecular structure, and reactivity of the isolable silylenoid with a tricoordinate silicon. J. Am. Chem. Soc. 2006, 128, 2784-2785
  13. Lee, M.; Hyeon, M.; Lim, Y.; Choi, J.; Park, C.; Jeong, S.; Lee, U. Syntheses and reactivities of stable halosilylenoids, (Tsi)X2SiLi (Tsi = C(SiMe3)3, X = Br, Cl). Chem. Eur. J. 2004, 10, 377-381
  14. Qi, Y. H.; Ma, J.; Xu, C. J.; Geng, B.; He, M. X. Computational in