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231223s2008 xx |||||o 00| ||eng c |
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|a 10.1021/la800080b
|2 doi
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|a pubmed24n0600.xml
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|a (DE-627)NLM179831143
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|a (NLM)18507407
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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1 |
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|a von Wrochem, Florian
|e verfasserin
|4 aut
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|a Structure and conductance of aromatic and aliphatic dithioacetamide monolayers on Au(111)
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|c 2008
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 15.08.2008
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|a Date Revised 21.11.2013
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a The structure and electrical properties of self-assembled monolayers of cyclic aromatic and aliphatic dithioacetamides (1,4-bis(mercaptoacetamido)benzene and 1,4-bis(mercaptoacetamido)cyclohexane) and of mixed dithioacetamide/alkanethiol monolayers are characterized by X-ray photoelectron spectroscopy (XPS), scanning tunneling microscopy (STM) and contact angle goniometry. Both dithioacetamides are found to pack densely on Au(111), however the monolayers are poorly ordered as a result of hydrogen bond formation between the amide groups. The coassembly and the insertion method are compared for the formation of mixed dithioacetamide/alkanethiol monolayers. By coassembly, islands of dithioacetamides in a dodecanethiol matrix can only be obtained at a low dithioacetamide/dodecanethiol concentration ratio in solution (1/10) and by thermal annealing of the resulting monolayers. Small and well defined dithioacetamide domains are realized by insertion of dithioacetamides into defect sites of closely packed octanethiol monolayers. These domains are used to determine the molecular conductance by means of STM height profiles and molecular lengths resulting from density functional theory (DFT) calculations. The difference in the tunneling decay constant beta measured for aromatic dithioacetamides (beta = 0.74-0.76/A) and for aliphatic dithioacetamides (beta = 0.84-0.91/A) highlights the influence of the conjugation within the cyclic core on molecular conductance
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|a Journal Article
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|a Thioacetamide
|2 NLM
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|a 075T165X8M
|2 NLM
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|a Gold
|2 NLM
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|a 7440-57-5
|2 NLM
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| 700 |
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|a Scholz, Frank
|e verfasserin
|4 aut
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|a Schreiber, Akos
|e verfasserin
|4 aut
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|a Nothofer, Heinz-Georg
|e verfasserin
|4 aut
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|a Ford, William E
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Morf, Peter
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Jung, Thomas
|e verfasserin
|4 aut
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|a Yasuda, Akio
|e verfasserin
|4 aut
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|a Wessels, Jurina M
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 24(2008), 13 vom: 01. Juni, Seite 6910-7
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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| 773 |
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|g volume:24
|g year:2008
|g number:13
|g day:01
|g month:06
|g pages:6910-7
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|u http://dx.doi.org/10.1021/la800080b
|3 Volltext
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