Dewar benzene【有化】 - PMC

Tomáš Slanina, Rabia Ayub, Josene Toldo, Johan Sundell, Wangchuk Rabten, Marco Nicaso, Igor Alabugin, Ignacio Fdez. Galván, Arvind K. Gupta, Roland Lindh, Andreas Orthaber, Richard J. Lewis, Gunnar Grönberg, Joakim Bergman, Henrik Ottosson

J Am Chem Soc. 2020 Jun 24; 142(25): 10942–10954. Published online 2020 May 27. doi: 10.1021/jacs.9b13769

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The non-adiabatic nanoreactor: towards the automated discovery of photochemistry

Elisa Pieri, Dean Lahana, Alexander M. Chang, Cody R. Aldaz, Keiran C. Thompson, Todd J. Martínez

Chem Sci. 2021 Jun 2; 12(21): 7294–7307. Published online 2021 Apr 29. doi: 10.1039/d1sc00775k

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Indirect validation of benzene exposure assessment by association with benzene poisoning.

M Dosemeci, S N Yin, M Linet, S Wacholder, N Rothman, G L Li, W H Chow, Y Z Wang, Z L Jiang, T R Dai, W U Zhang, X J Chao, P Z Ye, Q R Kou, Y H Fan, X C Zhang, X F Lin, J F Meng, J S Zho, W J Blot, R B Hayes

Environ Health Perspect. 1996 Dec; 104(Suppl 6): 1343–1347. doi: 10.1289/ehp.961041343

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Rupturing aromaticity by periphery overcrowding

Promeet K. Saha, Abhijit Mallick, Andrew T. Turley, Aisha N. Bismillah, Andrew Danos, Andrew P. Monkman, Alyssa-Jennifer Avestro, Dmitry S. Yufit, Paul R. McGonigal

Nat Chem. 2023; 15(4): 516–525. Published online 2023 Mar 6. doi: 10.1038/s41557-023-01149-6

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The nature of cation-pi binding: interactions between tetramethylammonium ion and benzene in aqueous solution.

J Gao, L W Chou, A Auerbach

Biophys J. 1993 Jul; 65(1): 43–47. doi: 10.1016/S0006-3495(93)81031-2

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Are Multicentre Bond Indices and Related Quantities Reliable Predictors of Excited-State Aromaticity?

Robert Ponec, David L. Cooper, Peter B. Karadakov

Molecules. 2020 Oct; 25(20): 4791. Published online 2020 Oct 19. doi: 10.3390/molecules25204791

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Dewar Heterocycles as Versatile Monomers for Ring-Opening Metathesis Polymerization

Sepand K. Nistanaki, Hosea M. Nelson

ACS Macro Lett. Author manuscript; available in PMC 2021 Jul 22.

Published in final edited form as: ACS Macro Lett. 2020 May 19; 9(5): 731–735. Published online 2020 May 1. doi: 10.1021/acsmacrolett.0c00227

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An Iron‐Catalyzed Route to Dewar 1,3,5‐Triphosphabenzene and Subsequent Reactivity

Adam N. Barrett, Dr. Martin Diefenbach, Mary F. Mahon, Prof. Dr. Vera Krewald, Dr. Ruth L. Webster

Angew Chem Int Ed Engl. 2022 Sep 12; 61(37): e202208663. Published online 2022 Aug 9. doi: 10.1002/anie.202208663

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Ab initio dynamics and photoionization mass spectrometry reveal ion–molecule pathways from ionized acetylene clusters to benzene cation

Tamar Stein, Biswajit Bandyopadhyay, Tyler P. Troy, Yigang Fang, Oleg Kostko, Musahid Ahmed, Martin Head-Gordon

Proc Natl Acad Sci U S A. 2017 May 23; 114(21): E4125–E4133. Published online 2017 May 8. doi: 10.1073/pnas.1616464114

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Possible Roles of Transition Metal Cations in the Formation of Interstellar Benzene via Catalytic Acetylene Cyclotrimerization

Tatsuhiro Murakami, Naoki Matsumoto, Takashi Fujihara, Toshiyuki Takayanagi

Molecules. 2023 Nov; 28(21): 7454. Published online 2023 Nov 6. doi: 10.3390/molecules28217454

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The activation efficiency of mechanophores can be modulated by adjacent polymer composition

Sourabh Kumar, Tim Stauch

RSC Adv. 2021 Feb 10; 11(13): 7391–7396. Published online 2021 Feb 12. doi: 10.1039/d0ra09834e

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Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation

Evgenia Vaganova, Dror Eliaz, Ulyana Shimanovich, Gregory Leitus, Emad Aqad, Vladimir Lokshin, Vladimir Khodorkovsky

Molecules. 2021 Nov; 26(22): 6925. Published online 2021 Nov 17. doi: 10.3390/molecules26226925

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Pervaporation and Gas Separation Properties of High-Molecular Ladder-like Polyphenylsilsesquioxanes

Tatiana S. Anokhina, Tatyana O. Ershova, Anton A. Anisimov, Maxim N. Temnikov, Evgenia A. Grushevenko, Ilya L. Borisov, Alexey V. Volkov, Aziz M. Muzafarov

Polymers (Basel) 2023 Aug; 15(15): 3277. Published online 2023 Aug 2. doi: 10.3390/polym15153277

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Cation-pi interactions in aromatics of biological and medicinal interest: electrostatic potential surfaces as a useful qualitative guide.

S Mecozzi, A P West, Jr, D A Dougherty

Proc Natl Acad Sci U S A. 1996 Oct 1; 93(20): 10566–10571. doi: 10.1073/pnas.93.20.10566

PMCID:: PMC38193

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Ring opening of 2-aza-3-borabicyclo[2.2.0]hex-5-ene, the Dewar form of 1,2-dihydro-1,2-azaborine: stepwise versus concerted mechanisms

Holger F Bettinger, Otto Hauler

Beilstein J Org Chem. 2013; 9: 761–766. Published online 2013 Apr 18. doi: 10.3762/bjoc.9.86

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A trypsin-like platelet protease propagates protease-activated receptor-1 cleavage and platelet activation.

F A Ofosu, J Freedman, L Dewar, Y Song, J W Fenton, 2nd

Biochem J. 1998 Dec 1; 336(Pt 2): 283–285. doi: 10.1042/bj3360283

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The Dewar Isomer of 1,2-Dihydro-1,2-azaborinines: Isolation, Fragmentation, and Energy Storage

Klara Edel, Xinyu Yang, Jacob S. A. Ishibashi, Ashley N. Lamm, Cäcilia Maichle-Mössmer, Zachary X. Giustra, Shih-Yuan Liu, Holger F. Bettinger

Angew Chem Int Ed Engl. Author manuscript; available in PMC 2019 May 4.

Published in final edited form as: Angew Chem Int Ed Engl. 2018 May 4; 57(19): 5296–5300. Published online 2018 Mar 30. doi: 10.1002/anie.201712683

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High Efficiency Membranes Based on PTMSP and Hyper-Crosslinked Polystyrene for Toxic Volatile Compounds Removal from Wastewater

Georgy Golubev, Stepan Sokolov, Tatyana Rokhmanka, Sergey Makaev, Ilya Borisov, Svetlana Khashirova, Alexey Volkov

Polymers (Basel) 2022 Jul; 14(14): 2944. Published online 2022 Jul 20. doi: 10.3390/polym14142944

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Scheme 1

Isomerisation of bicyclo[2.2.0]hexa-1,3-diene, Dewar benzene (1), to benzene (2) and of 2-aza-3-borabicyclo[2.2.0]hex-5-ene (3) to 1,2-dihydro-1,2-azaborine (4).

Ring opening of 2-aza-3-borabicyclo[2.2.0]hex-5-ene, the Dewar form of 1,2-dihydro-1,2-azaborine: stepwise versus concerted mechanisms

Beilstein J Org Chem. 2013;9:761-766.
Fig. 3Fluorobenzene transforming into fluor Dewar benzene.

Synchronizing chemistry, quantum mechanics and radioactivity in a revolutionary renewed atom model. Part 1: the elements where Z is 1–10 (H, He, Li, Be, B, C, N, O, F, Ne)

RSC Adv. 2021 Aug 16;11(45):27978-27991.
Fig. 5Stationary points identified on S0 by the NANR; fulvene and Dewar benzene were not discovered by the nanoreactor, and are added for comparison. All energies are referenced to the S0 equilibrium geometry of benzene at their respective level of theory.

The non-adiabatic nanoreactor: towards the automated discovery of photochemistry

Chem Sci. 2021 Jun 2;12(21):7294-7307.
Fig. 1Mechanical activation pathways of the investigated mechanophores (a: Dewar benzene, b: benzocyclobutene, c: gem-dichlorocyclopropane) and investigated linkers.

The activation efficiency of mechanophores can be modulated by adjacent polymer composition

RSC Adv. 2021 Feb 10;11(13):7391-7396.