A mechanochemical study of the effects of compression on a Diels-Alder reaction

被引:22
|
作者
Jha, Sanjiv K. [1 ]
Brown, Katie [2 ]
Todde, Guido [1 ]
Subramanian, Gopinath [1 ]
机构
[1] Univ Southern Mississippi, Sch Polymers & High Performance Mat, Hattiesburg, MS 39402 USA
[2] Auburn Univ, Dept Polymer & Fiber Engn, Auburn, AL 36849 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 145卷 / 07期
基金
美国国家科学基金会;
关键词
MOLECULE FORCE SPECTROSCOPY; ELASTIC BAND METHOD; STEPWISE MECHANISMS; TRANSITION-STATES; MALEIC-ANHYDRIDE; PRESSURE; BUTADIENE; ETHYLENE; VINYLCYCLOBUTANE; CYCLOADDITION;
D O I
10.1063/1.4960955
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We examine the effects of compressive external forces on the mechanisms of the parent Diels-Alder (DA) reaction between butadiene and ethylene. Reaction pathways and transition states were calculated using the nudged elastic band method within a mechanochemical framework at the CASSCF(6,6)/6-31G**, as well as the B3LYP/6-311++G** levels of theory. Our results suggest that compressive hydrostatic pressure lowers the energy barrier for the parent DA reaction while suppressing the undesirable side reaction, thereby leading to a direct increase in the yield of cyclohexene. Compressive pressure also increases the exothermicity of the parent DA reaction, which would lead to increased temperatures in a reaction vessel and thereby indirectly increase the yield of cyclohexene. Our estimates indicate that the compression used in our study corresponds to a range of 68 MPa-1410 MPa. Published by AIP Publishing.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Theoretical Study of Diels-Alder Reaction: Role of Substituent in Regioselectivity and Aromaticity
    Mohajeri, A.
    Shahamirian, M.
    JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2010, 7 (03) : 554 - 563
  • [2] Study on Diels-Alder reaction of nitrosoalkenes
    Tang, Xiaoxiao
    Lu, Baozhao
    Chen, Yu
    Wang, Jiexue
    Jin, Liming
    Yang, Hongjun
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2023, 59 (11-12) : 811 - 815
  • [3] Recrossing and Dynamic Matching Effects on Selectivity in a Diels-Alder Reaction
    Wang, Zhihong
    Hirschi, Jennifer S.
    Singleton, Daniel A.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (48) : 9156 - 9159
  • [4] Dehydrogenative Diels-Alder Reaction
    Ozawa, Takuya
    Kurahashi, Takuya
    Matsubara, Seijiro
    ORGANIC LETTERS, 2011, 13 (19) : 5390 - 5393
  • [5] Industrial Applications of the Diels-Alder Reaction
    Funel, Jacques-Alexis
    Abele, Stefan
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (14) : 3822 - 3863
  • [6] Diels-Alder and Formal Diels-Alder Cycloaddition Reactions of Ynamines and Ynamides
    Duret, Guillaume
    Le Fouler, Vincent
    Bisseret, Philippe
    Bizet, Vincent
    Blanchard, Nicolas
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2017, 2017 (46) : 6816 - 6830
  • [7] Fluoropropenoates as dienophiles in the Diels-Alder reaction
    Patrick, Timothy B.
    Fianu, Cynthia
    Pak, Eric
    Zaksas, Kasey
    Neal, Bradley E.
    JOURNAL OF FLUORINE CHEMISTRY, 2006, 127 (07) : 861 - 864
  • [8] The Diels-Alder reaction in total synthesis
    Nicolaou, KC
    Snyder, SA
    Montagnon, T
    Vassilikogiannakis, G
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2002, 41 (10) : 1668 - 1698
  • [9] An on-surface Diels-Alder reaction
    Castro-Esteban, Jesus
    Albrecht, Florian
    Fatayer, Shadi
    Perez, Dolores
    Gross, Leo
    Pena, Diego
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (50) : 26346 - 26350
  • [10] An ab initio analysis of the Diels-Alder reaction between two isoprenes
    Wang, Chuan-Ming
    Liu, Zhi-Hua
    Chen, Yong-Kuan
    Han, Jing-Mei
    Chen, Yi-Lei
    Miao, Ming-Ming
    Cao, Huai
    COMPUTATIONAL AND THEORETICAL CHEMISTRY, 2013, 1017 : 174 - 181