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Detecting mechanochemical atropisomerization within an STM break junction.

Abstract:
We have employed the scanning tunneling microscope break-junction technique to investigate the single-molecule conductance of a family of 5,15-diaryl porphyrins bearing thioacetyl (SAc) or methylsulfide (SMe) binding groups at the ortho position of the phenyl rings (S2 compounds). These ortho substituents lead to two atropisomers, cis and trans, for each compound, which do not interconvert in solution under ambient conditions; even at high temperatures, isomerization takes several hours (half-life 15 h at 140 °C for SAc in C2Cl4D2). All the S2 compounds exhibit two conductance groups, and comparison with a monothiolated (S1) compound shows the higher group arises from a direct Au-porphyrin interaction. The lower conductance group is associated with the S-to-S pathway. When the binding group is SMe, the difference in junction length distribution reflects the difference in S-S distance (0.3 nm) between the two isomers. In the case of SAc, there are no significant differences between the plateau length distributions of the two isomers, and both show maximal stretching distances well exceeding their calculated junction lengths. Contact deformation accounts for part of the extra length, but the results indicate that cis-to-trans conversion takes place in the junction for the cis isomer. The barrier to atropisomerization is lower than the strength of the thiolate Au-S and Au-Au bonds, but higher than that of the Au-SMe bond, which explains why the strain in the junction only induces isomerization in the SAc compound.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/jacs.7b10542

Authors

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Role:
Author
ORCID:
0000-0001-7541-5997
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Institution:
University of Oxford
Division:
MPLS Division
Department:
Chemistry; Organic Chemistry
Role:
Author


Publisher:
American Chemical Society
Journal:
Journal of the American Chemical Society More from this journal
Volume:
140
Issue:
2
Pages:
710-718
Publication date:
2017-12-01
Acceptance date:
2017-12-20
DOI:
EISSN:
1520-5126
ISSN:
0002-7863
Pmid:
29260871


Language:
English
Keywords:
Pubs id:
pubs:813600
UUID:
uuid:1eeb1170-4e1e-49a0-83a9-3c4a0697cee4
Local pid:
pubs:813600
Source identifiers:
813600
Deposit date:
2018-02-10
ARK identifier:

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