Synthesis, electronic properties and self-assembly on Au{111} of thiolated (oligo)phenothiazines

Adam W. Franz, Svetlana Stoycheva, Michael Himmelhaus and Thomas J. J. Müller
Beilstein J. Org. Chem. 2010, 6, No. 72.

Supporting Information

Supporting Information File 1: Molecular modeling coordinates of 2a, 2c, 2d, 2e, and 4, cyclic voltammograms of 2a, 2b, 2c, 2d, 2e, and 4, and absorption and emission spectra of 2d and 2e.
Format: PDF Size: 407.4 KB Download

Cite the Following Article

Synthesis, electronic properties and self-assembly on Au{111} of thiolated (oligo)phenothiazines
Adam W. Franz, Svetlana Stoycheva, Michael Himmelhaus and Thomas J. J. Müller
Beilstein J. Org. Chem. 2010, 6, No. 72.

How to Cite

Franz, A. W.; Stoycheva, S.; Himmelhaus, M.; Müller, T. J. J. Beilstein J. Org. Chem. 2010, 6, No. 72. doi:10.3762/bjoc.6.72

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • May, L.; Müller, T. Electron-Rich Phenothiazine Congeners and Beyond: Synthesis and Electronic Properties of Isomeric Dithieno[1,4]thiazines. Chemistry (Weinheim an der Bergstrasse, Germany) 2020, 26, 12111–12118. doi:10.1002/chem.202000137
  • Moll, B.; Tichelkamp, T.; Wegner, S.; Francis, B.; Müller, T.; Janiak, C. Near-infrared (NIR) surface-enhanced Raman spectroscopy (SERS) study of novel functional phenothiazines for potential use in dye sensitized solar cells (DSSC). RSC advances 2019, 9, 37365–37375. doi:10.1039/c9ra08675g
  • Perini, C. J.; Basnet, P.; West, M. P.; Vogel, E. M. Impact of Synthesized MoS2 Wafer-Scale Quality on Fermi Level Pinning in Vertical Schottky-Barrier Heterostructures. ACS applied materials & interfaces 2018, 10, 39860–39871. doi:10.1021/acsami.8b13112
  • Shard, A.; Kumar, R.; Equbal, D.; Sinha, A. K. Pot‐Economical Synthesis of Hydroxylated Arylethenyl‐arylethynyl‐arenes through Sequential Decarboxylative Perkin–Sonogashira Reactions. Asian Journal of Organic Chemistry 2017, 7, 189–196. doi:10.1002/ajoc.201700504
  • Schneeweis, A. P. W.; Neidlinger, A.; Reiss, G. J.; Frank, W.; Heinze, K.; Müller, T. Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine. Organic Chemistry Frontiers 2017, 4, 839–846. doi:10.1039/c7qo00188f
  • Urselmann, D.; Deilhof, K.; Mayer, B.; Müller, T. Thiophene-forming one-pot synthesis of three thienyl-bridged oligophenothiazines and their electronic properties. Beilstein journal of organic chemistry 2016, 12, 2055–2064. doi:10.3762/bjoc.12.194
  • Rechmann, J.; Sarfraz, A.; Götzinger, A. C.; Dirksen, E.; Müller, T.; Erbe, A. Surface Functionalization of Oxide-Covered Zinc and Iron with Phosphonated Phenylethynyl Phenothiazine. Langmuir : the ACS journal of surfaces and colloids 2015, 31, 7306–7316. doi:10.1021/acs.langmuir.5b01370
  • Rednic, M. I.; Hădade, N. D.; Bogdan, E.; Grosu, I. Macrocycles embedding phenothiazine or similar nitrogen and/or sulphur containing heterocycles. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2014, 81, 263–293. doi:10.1007/s10847-014-0455-x
  • Pereţeanu, I. S.; Müller, T. Synthesis and electronic properties of 3,7-dianilino substituted N-hexyl phenothiazines. Organic & biomolecular chemistry 2013, 11, 5127–5135. doi:10.1039/c3ob40815a
  • Medruţ, I.; Turdean, R.; Gropeanu, R.; Pop, F.; Toupet, L.; Hădade, N. D.; Bogdan, E.; Grosu, I. Macrocycles with a phenothiazine core: synthesis, structural analysis, and electronic properties. Tetrahedron Letters 2013, 54, 1107–1111. doi:10.1016/j.tetlet.2012.12.068
  • Bieliauskas, A.; Martynaitis, V.; Getautis, V.; Malinauskas, T.; Jankauskas, V.; Kamarauskas, E.; Holzer, W.; Šačkus, A. Synthesis of electroactive hydrazones derived from 3-(10-alkyl-10H-phenothiazin-3-yl)-2-propenals and their corresponding 3,3′-bispropenals. Tetrahedron 2012, 68, 3552–3559. doi:10.1016/j.tet.2012.03.010
  • Hauck, M.; Turdean, R.; Memminger, K.; Schönhaber, J.; Rominger, F.; Müller, T. Luminescent, Redox-Active Diphenothiazine Dumbbells Expanded by Conjugated Arenes and Heteroarenes. The Journal of organic chemistry 2010, 75, 8591–8603. doi:10.1021/jo101997t
Other Beilstein-Institut Open Science Activities