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Alkoxylated dehydrobenzo[12]annulene on Au(111): from single molecules to quantum dot molecular networks.

Chemical communications (Cambridge, England)

Schouteden K, Ivanova T, Li Z, Iancu V, Tahara K, Tobe Y, Adisoejoso J, De Feyter S, Van Haesendonck C, Janssens E.
PMID: 26060847
Chem Commun (Camb). 2015 Jul 11;51(54):10917-20. doi: 10.1039/c5cc03255e.

We demonstrate the effective confinement of surface electrons in the pores of molecular networks formed by dehydrobenzo[12]annulene (DBA) molecules with butoxy groups (DBA-OC4) on Au(111). Investigation of the network formation starting from single molecules reveals a considerable interaction of...

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Schouteden K, Ivanova T, Li Z, et al. Alkoxylated dehydrobenzo[12]annulene on Au(111): from single molecules to quantum dot molecular networks. Chem Commun (Camb). 2015;51(54):10917-20doi: 10.1039/c5cc03255e.
Schouteden, K., Ivanova, T., Li, Z., Iancu, V., Tahara, K., Tobe, Y., Adisoejoso, J., De Feyter, S., Van Haesendonck, C., & Janssens, E. (2015). Alkoxylated dehydrobenzo[12]annulene on Au(111): from single molecules to quantum dot molecular networks. Chemical communications (Cambridge, England), 51(54), 10917-20. https://doi.org/10.1039/c5cc03255e
Schouteden, Koen, et al. "Alkoxylated dehydrobenzo[12]annulene on Au(111): from single molecules to quantum dot molecular networks." Chemical communications (Cambridge, England) vol. 51,54 (2015): 10917-20. doi: https://doi.org/10.1039/c5cc03255e
Schouteden K, Ivanova T, Li Z, Iancu V, Tahara K, Tobe Y, Adisoejoso J, De Feyter S, Van Haesendonck C, Janssens E. Alkoxylated dehydrobenzo[12]annulene on Au(111): from single molecules to quantum dot molecular networks. Chem Commun (Camb). 2015 Jul 11;51(54):10917-20. doi: 10.1039/c5cc03255e. PMID: 26060847.
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Dynamic control over supramolecular handedness by selecting chiral induction pathways at the solution-solid interface.

Nature chemistry

Fang Y, Ghijsens E, Ivasenko O, Cao H, Noguchi A, Mali KS, Tahara K, Tobe Y, De Feyter S.
PMID: 27325099
Nat Chem. 2016 Jul;8(7):711-7. doi: 10.1038/nchem.2514. Epub 2016 May 09.

A dominant theme within the research on two-dimensional chirality is the sergeant-soldiers principle, wherein a small fraction of chiral molecules (sergeants) is used to skew the handedness of achiral molecules (soldiers) to generate a homochiral surface. Here, we have...

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Fang Y, Ghijsens E, Ivasenko O, et al. Dynamic control over supramolecular handedness by selecting chiral induction pathways at the solution-solid interface. Nat Chem. 2016;8(7):711-7doi: 10.1038/nchem.2514.
Fang, Y., Ghijsens, E., Ivasenko, O., Cao, H., Noguchi, A., Mali, K. S., Tahara, K., Tobe, Y., & De Feyter, S. (2016). Dynamic control over supramolecular handedness by selecting chiral induction pathways at the solution-solid interface. Nature chemistry, 8(7), 711-7. https://doi.org/10.1038/nchem.2514
Fang, Yuan, et al. "Dynamic control over supramolecular handedness by selecting chiral induction pathways at the solution-solid interface." Nature chemistry vol. 8,7 (2016): 711-7. doi: https://doi.org/10.1038/nchem.2514
Fang Y, Ghijsens E, Ivasenko O, Cao H, Noguchi A, Mali KS, Tahara K, Tobe Y, De Feyter S. Dynamic control over supramolecular handedness by selecting chiral induction pathways at the solution-solid interface. Nat Chem. 2016 Jul;8(7):711-7. doi: 10.1038/nchem.2514. Epub 2016 May 09. PMID: 27325099.
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Scanning probe microscopy induced surface modifications of the topological insulator Bi.

Nanotechnology

Netsou AM, Thupakula U, Debehets J, Chen T, Hirsch B, Volodin A, Li Z, Song F, Won Seo J, De Feyter S, Schouteden K, Van Haesendonck C.
PMID: 28656908
Nanotechnology. 2017 Aug 18;28(33):335706. doi: 10.1088/1361-6528/aa7c28. Epub 2017 Jun 28.

We investigated the topological insulator (TI) Bi

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Netsou AM, Thupakula U, Debehets J, et al. Scanning probe microscopy induced surface modifications of the topological insulator Bi. Nanotechnology. 2017;28(33):335706doi: 10.1088/1361-6528/aa7c28.
Netsou, A. M., Thupakula, U., Debehets, J., Chen, T., Hirsch, B., Volodin, A., Li, Z., Song, F., Won Seo, J., De Feyter, S., Schouteden, K., & Van Haesendonck, C. (2017). Scanning probe microscopy induced surface modifications of the topological insulator Bi. Nanotechnology, 28(33), 335706. https://doi.org/10.1088/1361-6528/aa7c28
Netsou, Asteriona-Maria, et al. "Scanning probe microscopy induced surface modifications of the topological insulator Bi." Nanotechnology vol. 28,33 (2017): 335706. doi: https://doi.org/10.1088/1361-6528/aa7c28
Netsou AM, Thupakula U, Debehets J, Chen T, Hirsch B, Volodin A, Li Z, Song F, Won Seo J, De Feyter S, Schouteden K, Van Haesendonck C. Scanning probe microscopy induced surface modifications of the topological insulator Bi. Nanotechnology. 2017 Aug 18;28(33):335706. doi: 10.1088/1361-6528/aa7c28. Epub 2017 Jun 28. PMID: 28656908.
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Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles.

Chemistry (Weinheim an der Bergstrasse, Germany)

Schwab MG, Takase M, Mavrinsky A, Pisula W, Feng X, Gámez JA, Thiel W, Mali KS, de Feyter S, Müllen K.
PMID: 25867924
Chemistry. 2015 Jun 01;21(23):8426-34. doi: 10.1002/chem.201406602. Epub 2015 Apr 13.

A series of novel toroidal cyclo-2,9-tris-1,10-phenanthroline macrocycles with an unusual hexaaza cavity are reported. Nickel-mediated Yamamoto aryl-aryl coupling was found to be a versatile tool for the cyclotrimerization of functionalized 1,10-phenathroline precursors. Due to the now improved processability, both...

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Schwab MG, Takase M, Mavrinsky A, et al. Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry. 2015;21(23):8426-34doi: 10.1002/chem.201406602.
Schwab, M. G., Takase, M., Mavrinsky, A., Pisula, W., Feng, X., Gámez, J. A., Thiel, W., Mali, K. S., de Feyter, S., & Müllen, K. (2015). Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry (Weinheim an der Bergstrasse, Germany), 21(23), 8426-34. https://doi.org/10.1002/chem.201406602
Schwab, Matthias Georg, et al. "Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,23 (2015): 8426-34. doi: https://doi.org/10.1002/chem.201406602
Schwab MG, Takase M, Mavrinsky A, Pisula W, Feng X, Gámez JA, Thiel W, Mali KS, de Feyter S, Müllen K. Torands Revisited: Metal Sequestration and Self-Assembly of Cyclo-2,9-tris-1,10-phenanthroline Hexaaza Macrocycles. Chemistry. 2015 Jun 01;21(23):8426-34. doi: 10.1002/chem.201406602. Epub 2015 Apr 13. PMID: 25867924.
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Self-assembled air-stable supramolecular porous networks on graphene.

ACS nano

Li B, Tahara K, Adisoejoso J, Vanderlinden W, Mali KS, De Gendt S, Tobe Y, De Feyter S.
PMID: 24206021
ACS Nano. 2013 Dec 23;7(12):10764-72. doi: 10.1021/nn4039047. Epub 2013 Nov 18.

Functionalization and modification of graphene at the nanometer scale is desirable for many applications. Supramolecular assembly offers an attractive approach in this regard, as many organic molecules form well-defined patterns on surfaces such as graphite via physisorption. Here we...

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Li B, Tahara K, Adisoejoso J, et al. Self-assembled air-stable supramolecular porous networks on graphene. ACS Nano. 2013;7(12):10764-72doi: 10.1021/nn4039047.
Li, B., Tahara, K., Adisoejoso, J., Vanderlinden, W., Mali, K. S., De Gendt, S., Tobe, Y., & De Feyter, S. (2013). Self-assembled air-stable supramolecular porous networks on graphene. ACS nano, 7(12), 10764-72. https://doi.org/10.1021/nn4039047
Li, Bing, et al. "Self-assembled air-stable supramolecular porous networks on graphene." ACS nano vol. 7,12 (2013): 10764-72. doi: https://doi.org/10.1021/nn4039047
Li B, Tahara K, Adisoejoso J, Vanderlinden W, Mali KS, De Gendt S, Tobe Y, De Feyter S. Self-assembled air-stable supramolecular porous networks on graphene. ACS Nano. 2013 Dec 23;7(12):10764-72. doi: 10.1021/nn4039047. Epub 2013 Nov 18. PMID: 24206021.
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Formation of Multicomponent Star Structures at the Liquid/Solid Interface.

Langmuir : the ACS journal of surfaces and colloids

Tahara K, Kaneko K, Katayama K, Itano S, Nguyen CH, Amorim DD, De Feyter S, Tobe Y.
PMID: 26061362
Langmuir. 2015 Jun 30;31(25):7032-40. doi: 10.1021/acs.langmuir.5b01507. Epub 2015 Jun 19.

To demonstrate key roles of multiple interactions between multiple components and multiple phases in the formation of an uncommon self-assembling pattern, we present here the construction of a porous hexagonal star (h-star) structure using a trigonal molecular building block...

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Tahara K, Kaneko K, Katayama K, et al. Formation of Multicomponent Star Structures at the Liquid/Solid Interface. Langmuir. 2015;31(25):7032-40doi: 10.1021/acs.langmuir.5b01507.
Tahara, K., Kaneko, K., Katayama, K., Itano, S., Nguyen, C. H., Amorim, D. D., De Feyter, S., & Tobe, Y. (2015). Formation of Multicomponent Star Structures at the Liquid/Solid Interface. Langmuir : the ACS journal of surfaces and colloids, 31(25), 7032-40. https://doi.org/10.1021/acs.langmuir.5b01507
Tahara, Kazukuni, et al. "Formation of Multicomponent Star Structures at the Liquid/Solid Interface." Langmuir : the ACS journal of surfaces and colloids vol. 31,25 (2015): 7032-40. doi: https://doi.org/10.1021/acs.langmuir.5b01507
Tahara K, Kaneko K, Katayama K, Itano S, Nguyen CH, Amorim DD, De Feyter S, Tobe Y. Formation of Multicomponent Star Structures at the Liquid/Solid Interface. Langmuir. 2015 Jun 30;31(25):7032-40. doi: 10.1021/acs.langmuir.5b01507. Epub 2015 Jun 19. PMID: 26061362.
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Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly.

Chemical communications (Cambridge, England)

Li B, Puigmartí-Luis J, Jonas AM, Amabilino DB, De Feyter S.
PMID: 25027031
Chem Commun (Camb). 2014 Nov 11;50(87):13216-9. doi: 10.1039/c4cc03676j. Epub 2014 Jul 16.

Self-assembly of a TTF derivative capable of forming self-assembled monolayers at the surface of graphite displays hierarchical growth of multilayers and concentric nanorings upon evaporation of the solvent as observed by AFM.

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Li B, Puigmartí-Luis J, Jonas AM, et al. Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly. Chem Commun (Camb). 2014;50(87):13216-9doi: 10.1039/c4cc03676j.
Li, B., Puigmartí-Luis, J., Jonas, A. M., Amabilino, D. B., & De Feyter, S. (2014). Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly. Chemical communications (Cambridge, England), 50(87), 13216-9. https://doi.org/10.1039/c4cc03676j
Li, Bing, et al. "Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly." Chemical communications (Cambridge, England) vol. 50,87 (2014): 13216-9. doi: https://doi.org/10.1039/c4cc03676j
Li B, Puigmartí-Luis J, Jonas AM, Amabilino DB, De Feyter S. Hierarchical growth of curved organic nanowires upon evaporation induced self-assembly. Chem Commun (Camb). 2014 Nov 11;50(87):13216-9. doi: 10.1039/c4cc03676j. Epub 2014 Jul 16. PMID: 25027031.
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Anti-restenosis Trials.

Current interventional cardiology reports

de Feyter PJ, Vos J, Rensing BJ.
PMID: 11096683
Curr Interv Cardiol Rep. 2000 Nov;2(4):326-331.

The high frequency of restenosis after percutaneous coronary angioplasty is still a major clinical problem. It occurs in 30% to 60% of patients and limits the long-term success of angioplasty. Many clinical trials have been conducted to resolve this...

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de Feyter PJ, Vos J, Rensing BJ. Anti-restenosis Trials. Curr Interv Cardiol Rep. 2000;2(4):326-331
de Feyter PJ, Vos, J., & Rensing, B. J. (2000). Anti-restenosis Trials. Current interventional cardiology reports, 2(4), 326-331.
de Feyter PJ, et al. "Anti-restenosis Trials." Current interventional cardiology reports vol. 2,4 (2000): 326-331.
de Feyter PJ, Vos J, Rensing BJ. Anti-restenosis Trials. Curr Interv Cardiol Rep. 2000 Nov;2(4):326-331. PMID: 11096683.
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Synthesis, separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative.

Chemical communications (Cambridge, England)

Gomar-Nadal E, Abdel-Mottaleb MM, De Feyter S, Veciana J, Rovira C, Amabilino DB, De Schryver FC.
PMID: 12739671
Chem Commun (Camb). 2003 Apr 07;(7):906-7. doi: 10.1039/b300731f.

The synthesis, isolation and STM imaging on graphite of the cis and trans isomers of a TTF reveal isomer-dependent packing, and constitutes a way to study the non-covalent interactions at play in these systems.

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Gomar-Nadal E, Abdel-Mottaleb MM, De Feyter S, et al. Synthesis, separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative. Chem Commun (Camb). 2003;(7):906-7doi: 10.1039/b300731f.
Gomar-Nadal, E., Abdel-Mottaleb, M. M., De Feyter, S., Veciana, J., Rovira, C., Amabilino, D. B., & De Schryver, F. C. (2003). Synthesis, separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative. Chemical communications (Cambridge, England), (7), 906-7. https://doi.org/10.1039/b300731f
Gomar-Nadal, Elba, et al. "Synthesis, separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative." Chemical communications (Cambridge, England) vol. ,7 (2003): 906-7. doi: https://doi.org/10.1039/b300731f
Gomar-Nadal E, Abdel-Mottaleb MM, De Feyter S, Veciana J, Rovira C, Amabilino DB, De Schryver FC. Synthesis, separation, and isomer-dependent packing in two dimensions--detected by scanning tunnelling microscopy--of a TTF derivative. Chem Commun (Camb). 2003 Apr 07;(7):906-7. doi: 10.1039/b300731f. PMID: 12739671.
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Photoluminescence intensity fluctuations and electric-field-induced photoluminescence quenching in individual nanoclusters of poly(phenylenevinylene).

Chemphyschem : a European journal of chemical physics and physical chemistry

Scheblykin I, Zoriniants G, Hofkens J, De Feyter S, Van der Auweraer M, De Schryver FC.
PMID: 12674598
Chemphyschem. 2003 Mar 17;4(3):260-7. doi: 10.1002/cphc.200390042.

Substantial fluctuations of the fluorescence intensity have been detected for single clusters of poly(phenylenevinylene) containing more than 75 polymer chains or 30,000 monomer units. To the best of our knowledge, this is the first time such fluctuations (which resemble...

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Scheblykin I, Zoriniants G, Hofkens J, et al. Photoluminescence intensity fluctuations and electric-field-induced photoluminescence quenching in individual nanoclusters of poly(phenylenevinylene). Chemphyschem. 2003;4(3):260-7doi: 10.1002/cphc.200390042.
Scheblykin, I., Zoriniants, G., Hofkens, J., De Feyter, S., Van der Auweraer, M., & De Schryver, F. C. (2003). Photoluminescence intensity fluctuations and electric-field-induced photoluminescence quenching in individual nanoclusters of poly(phenylenevinylene). Chemphyschem : a European journal of chemical physics and physical chemistry, 4(3), 260-7. https://doi.org/10.1002/cphc.200390042
Scheblykin, Ivan, et al. "Photoluminescence intensity fluctuations and electric-field-induced photoluminescence quenching in individual nanoclusters of poly(phenylenevinylene)." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 4,3 (2003): 260-7. doi: https://doi.org/10.1002/cphc.200390042
Scheblykin I, Zoriniants G, Hofkens J, De Feyter S, Van der Auweraer M, De Schryver FC. Photoluminescence intensity fluctuations and electric-field-induced photoluminescence quenching in individual nanoclusters of poly(phenylenevinylene). Chemphyschem. 2003 Mar 17;4(3):260-7. doi: 10.1002/cphc.200390042. PMID: 12674598.
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Femtochemistry of Norrish type-I reactions: IV. Highly excited ketones--experimental.

Chemphyschem : a European journal of chemical physics and physical chemistry

Sølling TI, Diau EW, Kötting C, De Feyter S, Zewail AH.
PMID: 12465478
Chemphyschem. 2002 Jan 18;3(1):79-97. doi: 10.1002/1439-7641(20020118)3:1<79::AID-CPHC79>3.0.CO;2-#.

Femtosecond dynamics of Norrish type-I reactions of cyclic and acyclic ketones have been investigated in real time for a series of 13 compounds using femtosecond-resolved time-of-flight mass spectrometry. A general physical description of the ultrafast processes of ketones excited...

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Sølling TI, Diau EW, Kötting C, et al. Femtochemistry of Norrish type-I reactions: IV. Highly excited ketones--experimental. Chemphyschem. 2002;3(1):79-97doi: 10.1002/1439-7641(20020118)3:1<79::AID-CPHC79>3.0.CO;2-#.
Sølling, T. I., Diau, E. W., Kötting, C., De Feyter, S., & Zewail, A. H. (2002). Femtochemistry of Norrish type-I reactions: IV. Highly excited ketones--experimental. Chemphyschem : a European journal of chemical physics and physical chemistry, 3(1), 79-97. https://doi.org/10.1002/1439-7641(20020118)3:1<79::AID-CPHC79>3.0.CO;2-#
Sølling, Theis I, et al. "Femtochemistry of Norrish type-I reactions: IV. Highly excited ketones--experimental." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 3,1 (2002): 79-97. doi: https://doi.org/10.1002/1439-7641(20020118)3:1<79::AID-CPHC79>3.0.CO;2-#
Sølling TI, Diau EW, Kötting C, De Feyter S, Zewail AH. Femtochemistry of Norrish type-I reactions: IV. Highly excited ketones--experimental. Chemphyschem. 2002 Jan 18;3(1):79-97. doi: 10.1002/1439-7641(20020118)3:1<79::AID-CPHC79>3.0.CO;2-#. PMID: 12465478.
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Ultrasound Appearances of Coronary Stents as Obtained by Three-Dimensional Intracoronary Ultrasound Imaging In Vitro.

The Journal of invasive cardiology

Bruining N, von Birgelen C, de Feyter PJ, Roelandt JR, Serruys PW.
PMID: 10762809
J Invasive Cardiol. 1998 Jul;10(6):332-338.

Intracoronary ultrasound (ICUS) is an imaging technique which can provide a cross-sectional image of coronary arteries and implanted stents. Different stents may have individual ICUS imaging characteristics. To investigate the imaging characteristics and three-dimensional (3-D) reconstruction of different coronary...

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Bruining N, von Birgelen C, de Feyter PJ, et al. Ultrasound Appearances of Coronary Stents as Obtained by Three-Dimensional Intracoronary Ultrasound Imaging In Vitro. J Invasive Cardiol. 1998;10(6):332-338
Bruining, N., von Birgelen C, de Feyter PJ, Roelandt, J. R., & Serruys, P. W. (1998). Ultrasound Appearances of Coronary Stents as Obtained by Three-Dimensional Intracoronary Ultrasound Imaging In Vitro. The Journal of invasive cardiology, 10(6), 332-338.
Bruining, et al. "Ultrasound Appearances of Coronary Stents as Obtained by Three-Dimensional Intracoronary Ultrasound Imaging In Vitro." The Journal of invasive cardiology vol. 10,6 (1998): 332-338.
Bruining N, von Birgelen C, de Feyter PJ, Roelandt JR, Serruys PW. Ultrasound Appearances of Coronary Stents as Obtained by Three-Dimensional Intracoronary Ultrasound Imaging In Vitro. J Invasive Cardiol. 1998 Jul;10(6):332-338. PMID: 10762809.
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Showing 1 to 12 of 301 entries