Literature DB >> 34155377

Controlled growth of ordered monolayers of N-heterocyclic carbenes on silicon.

Martin Franz1, Sandhya Chandola1,2,3, Maximilian Koy4, Robert Zielinski1,5, Hazem Aldahhak2, Mowpriya Das4, Matthias Freitag4, Uwe Gerstmann2, Denise Liebig1, Adrian Karl Hoffmann1, Maximilian Rosin1, Wolf Gero Schmidt2, Conor Hogan6,7, Frank Glorius8, Norbert Esser9,10, Mario Dähne11.   

Abstract

N-Heterocyclic carbenes (NHCs) are promising modifiers and anchors for surface functionalization and offer some advantages over thiol-based systems. Because of their strong binding affinity and high electron donation, NHCs can dramatically change the properties of the surfaces to which they are bonded. Highly ordered NHC monolayers have so far been limited to metal surfaces. Silicon, however, remains the element of choice in semiconductor devices and its modification is therefore of utmost importance for electronic industries. Here, a comprehensive study on the adsorption of NHCs on silicon is presented. We find covalently bound NHC molecules in an upright adsorption geometry and demonstrate the formation of highly ordered monolayers exhibiting good thermal stability and strong work function reductions. The structure and ordering of the monolayers is controlled by the substrate geometry and reactivity and in particular by the NHC side groups. These findings pave the way towards a tailor-made organic functionalization of silicon surfaces and, thanks to the high modularity of NHCs, new electronic and optoelectronic applications.

Entities:  

Year:  2021        PMID: 34155377     DOI: 10.1038/s41557-021-00721-2

Source DB:  PubMed          Journal:  Nat Chem        ISSN: 1755-4330            Impact factor:   24.427


  29 in total

1.  Carbene Ligands in Surface Chemistry: From Stabilization of Discrete Elemental Allotropes to Modification of Nanoscale and Bulk Substrates.

Authors:  Aleksandr V Zhukhovitskiy; Michelle J MacLeod; Jeremiah A Johnson
Journal:  Chem Rev       Date:  2015-09-22       Impact factor: 60.622

2.  Ultra stable self-assembled monolayers of N-heterocyclic carbenes on gold.

Authors:  Cathleen M Crudden; J Hugh Horton; Iraklii I Ebralidze; Olena V Zenkina; Alastair B McLean; Benedict Drevniok; Zhe She; Heinz-Bernhard Kraatz; Nicholas J Mosey; Tomohiro Seki; Eric C Keske; Joanna D Leake; Alexander Rousina-Webb; Gang Wu
Journal:  Nat Chem       Date:  2014-03-23       Impact factor: 24.427

3.  Quantum Mechanical Study of N-Heterocyclic Carbene Adsorption on Au Surfaces.

Authors:  Kuan Chang; Jingguang G Chen; Qi Lu; Mu-Jeng Cheng
Journal:  J Phys Chem A       Date:  2017-03-27       Impact factor: 2.781

4.  An overview of N-heterocyclic carbenes.

Authors:  Matthew N Hopkinson; Christian Richter; Michael Schedler; Frank Glorius
Journal:  Nature       Date:  2014-06-26       Impact factor: 49.962

5.  Ballbot-type motion of N-heterocyclic carbenes on gold surfaces.

Authors:  Gaoqiang Wang; Andreas Rühling; Saeed Amirjalayer; Marek Knor; Johannes Bruno Ernst; Christian Richter; Hong-Jun Gao; Alexander Timmer; Hong-Ying Gao; Nikos L Doltsinis; Frank Glorius; Harald Fuchs
Journal:  Nat Chem       Date:  2016-10-03       Impact factor: 24.427

6.  Elucidating the Binding Modes of N-Heterocyclic Carbenes on a Gold Surface.

Authors:  Anne Bakker; Alexander Timmer; Elena Kolodzeiski; Matthias Freitag; Hong Ying Gao; Harry Mönig; Saeed Amirjalayer; Frank Glorius; Harald Fuchs
Journal:  J Am Chem Soc       Date:  2018-09-18       Impact factor: 15.419

7.  Simple direct formation of self-assembled N-heterocyclic carbene monolayers on gold and their application in biosensing.

Authors:  Cathleen M Crudden; J Hugh Horton; Mina R Narouz; Zhijun Li; Christene A Smith; Kim Munro; Christopher J Baddeley; Christian R Larrea; Benedict Drevniok; Bheeshmon Thanabalasingam; Alastair B McLean; Olena V Zenkina; Iraklii I Ebralidze; Zhe She; Heinz-Bernhard Kraatz; Nicholas J Mosey; Lisa N Saunders; Akiko Yagi
Journal:  Nat Commun       Date:  2016-09-02       Impact factor: 14.919

8.  Determination of the structure and geometry of N-heterocyclic carbenes on Au(111) using high-resolution spectroscopy.

Authors:  Giacomo Lovat; Evan A Doud; Deyu Lu; Gregor Kladnik; Michael S Inkpen; Michael L Steigerwald; Dean Cvetko; Mark S Hybertsen; Alberto Morgante; Xavier Roy; Latha Venkataraman
Journal:  Chem Sci       Date:  2018-11-05       Impact factor: 9.825

9.  N-Heterocyclic Carbene Self-assembled Monolayers on Copper and Gold: Dramatic Effect of Wingtip Groups on Binding, Orientation and Assembly.

Authors:  Christian R Larrea; Christopher J Baddeley; Mina R Narouz; Nicholas J Mosey; J Hugh Horton; Cathleen M Crudden
Journal:  Chemphyschem       Date:  2017-11-02       Impact factor: 3.102

10.  N-Heterocyclic carbenes on close-packed coinage metal surfaces: bis-carbene metal adatom bonding scheme of monolayer films on Au, Ag and Cu.

Authors:  Li Jiang; Bodong Zhang; Guillaume Médard; Ari Paavo Seitsonen; Felix Haag; Francesco Allegretti; Joachim Reichert; Bernhard Kuster; Johannes V Barth; Anthoula C Papageorgiou
Journal:  Chem Sci       Date:  2017-09-28       Impact factor: 9.825

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  3 in total

1.  Highly Ordered N-Heterocyclic Carbene Monolayers on Cu(111).

Authors:  Eloise Angove; Federico Grillo; Herbert A Früchtl; Alex J Veinot; Ishwar Singh; J Hugh Horton; Cathleen M Crudden; Christopher J Baddeley
Journal:  J Phys Chem Lett       Date:  2022-02-24       Impact factor: 6.475

2.  Covalent Adsorption of N-Heterocyclic Carbenes on a Copper Oxide Surface.

Authors:  Juan J Navarro; Mowpriya Das; Sergio Tosoni; Felix Landwehr; Jared P Bruce; Markus Heyde; Gianfranco Pacchioni; Frank Glorius; Beatriz Roldan Cuenya
Journal:  J Am Chem Soc       Date:  2022-09-01       Impact factor: 16.383

3.  Growth of N-Heterocyclic Carbene Assemblies on Cu(100) and Cu(111): From Single Molecules to Magic-Number Islands.

Authors:  Juan J Navarro; Mowpriya Das; Sergio Tosoni; Felix Landwehr; Maximilian Koy; Markus Heyde; Gianfranco Pacchioni; Frank Glorius; Beatriz Roldan Cuenya
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-10       Impact factor: 16.823

  3 in total

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