Literature DB >> 31173416

Linear Relationship between 13 C NMR Chemical Shifts and the Bending of sp-Carbon Chains.

Mathis Kreuzahler1, Abdulselam Adam1, Gebhard Haberhauer1.   

Abstract

Polyynes show a strictly linear relationship between the energy impact and the bending of the polyyne chain. The energy, which is necessary to bend the acetylenic chain, decreases with the increasing number of acetylene units. A deviation from linearity in polyynes can be realized in solution by violation of the mutual-exclusion principle between IR and Raman spectra. However, there is still no possibility to measure the extent of the nonlinearity in solution. Herein, we show that the 13 C NMR spectroscopy represents an appropriate tool for this as we found an almost perfect linear relationship between the bending of the alkyne chain and the change of the chemical shift of the outer acetylenic carbon atoms. By using molecular bows in which the alkyne chain can be bent by switching the azobenzene unit, this correlation can be proved experimentally. In the future, this correlation should enable the determination of the extent of the bending and the strain energy in polyynes. Consequently, polyynes could be employed as probes for measuring further molecular forces.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  DFT calculations; NMR spectroscopy; ab initio calculations; acetylenes; alkynes

Year:  2019        PMID: 31173416     DOI: 10.1002/chem.201902617

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Bicyclic Phenyl-Ethynyl Architectures: Synthesis of a 1,4-Bis(phenylbuta-1,3-diyn-1-yl) Benzene Banister.

Authors:  Linda Maria Bannwart; Thomas Müntener; Michel Rickhaus; Lukas Jundt; Daniel Häussinger; Marcel Mayor
Journal:  Chemistry       Date:  2021-03-03       Impact factor: 5.236

  1 in total

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