[reaction: see text] The first X-ray crystal structure of a mononuclear metallacyclopentadiene(alkyne) complex has been obtained. This type of metallacycle is believed to be the key intermediate in the cobalt-mediated [2 + 2 + 2]cycloaddition of alkynes. Thermal treatment leads to the generation of angular [4]phenylene, the X-ray structural details of which are described. Under photochemical conditions, the cobaltacycle isomerizes to a highly strained (cyclobutadieno)dibenzocyclooctatrienyne complex.
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http://dx.doi.org/10.1021/ol025956o | DOI Listing |
Dalton Trans
March 2024
Department of Chemistry, Indian Institute of Technology, Kharagpur-721302, India.
Herein, the first report on gel-to-gel transformations [2 + 2] photopolymerization in MOGs of metal halides and rigid dienes is presented. The MOGs and their xerogels show exceptional ability to undergo [2 + 2] polymerisation upon UV irradiation. Gel-to-gel transformations are very rare as the post-modification of gelators weakens the gel and transforms it to a sol.
View Article and Find Full Text PDFPhys Chem Chem Phys
May 2022
Heidelberg Institute for Theoretical Studies, Am Schlosswolfsbrunnenweg 35, 69118 Heidelberg, Germany.
Poly(-phenylene ethynylene)s, or short PPEs, are a class of conjugated and semi-flexible polymers with a strongly delocalized π electron system and increased chain stiffness. Due to this, PPEs have a wide range of technological applications. Although the material properties of single-chains or mixtures of few PPE chains have been studied in detail, the properties of large assemblies remain to be fully explored.
View Article and Find Full Text PDFOrg Chem Front
October 2020
Department of Chemistry, Marquette University, Milwaukee, WI 53201-1414, United States.
Herein, we report the synthesis of two new series of angular (all-syn) ladder-type -[n]phenylenes (LMP, n = 3-8). One series contains keto groups at the termini bridges, denoted angular keto (AKn), the second contains alkyl groups at all bridge sp carbons, denoted angular alkyl (AAn). Their electronic and structural properties were delineated by a combination of electrochemistry and spectroscopic (UV-Vis and emission) methods and further supported by DFT calculations.
View Article and Find Full Text PDFJ Org Chem
January 2018
Department of Chemistry and ‡Department of Environmental Science, University of San Francisco, 2130 Fulton Street, San Francisco, California 94117, United States.
Density functional and coupled cluster results are presented for hydrogen shifts in radicals derived from polycyclic aromatic hydrocarbons (PAHs) and for rearrangement mechanisms for several phenylenes. RCCSD(T)/cc-pVDZ//UBLYP/cc-pVDZ free energy barriers for 1,4-H shifts at 298 K are consistently predicted to be ca. 25 kcal/mol, whereas barriers for 1,5- and 1,6-shifts range from 6 to 28 kcal/mol.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2017
Department of Chemistry, National Cheng Kung University, No. 1 Ta-Hsueh Rd., 70101, Tainan, Taiwan.
This investigation demonstrates that a series of biphenylenes can be easily prepared from their corresponding halobiphenyls by the cyclization of in situ generated 2',3'-didehydro-2-lithiobiphenyls at low temperature. Two remarkable advantages of this synthetic method include 1) the lack of any need for transition-metal catalysts or reagents in the cyclization, and 2) the ability to obtain C1-functionalized products by treating the reaction intermediate 1-lithiobiphenylene with an electrophilic reagent. π-Extended derivatives, such as benzobiphenylenes, dibenzobiphenylene, linear/angular [3]phenylenes, and biphenyleno[2,3-b]biphenylenes, were synthesized similarly using suitable biaryls or teraryls.
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