Literature DB >> 17105258

Self-assembly of facially amphiphilic dendrimers on surfaces.

Yangbin Chen1, Ashootosh V Ambade, Dharma Rao Vutukuri, S Thayumanavan.   

Abstract

Facially amphiphilic dendrimers have been shown to provide significant difference in surface behavior due to subtle changes in structure. The monodendrons are capable of providing hydrophobic surfaces, while the didendrons provide superhydrophobic surfaces. This provides an example of how a molecular level change could result in significant changes in surface behavior. This difference is attributed to the conformational differences exhibited by these dendrimers on surfaces.

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Year:  2006        PMID: 17105258      PMCID: PMC2518940          DOI: 10.1021/ja065625x

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  7 in total

1.  Toward globular macromolecules with functionalized interiors: design and synthesis of dendrons with an interesting twist.

Authors:  P Bharathi; H Zhao; S Thayumanavan
Journal:  Org Lett       Date:  2001-06-14       Impact factor: 6.005

2.  Invertible amphiphilic homopolymers.

Authors:  Subhadeep Basu; Dharma Rao Vutukuri; Subarana Shyamroy; Britto S Sandanaraj; S Thayumanavan
Journal:  J Am Chem Soc       Date:  2004-08-18       Impact factor: 15.419

3.  A lotus-leaf-like superhydrophobic surface: a porous microsphere/nanofiber composite film prepared by electrohydrodynamics.

Authors:  Lei Jiang; Yong Zhao; Jin Zhai
Journal:  Angew Chem Int Ed Engl       Date:  2004-08-20       Impact factor: 15.336

4.  Dendrimers with both polar and apolar nanocontainer characteristics.

Authors:  Dharma Rao Vutukuri; Subhadeep Basu; S Thayumanavan
Journal:  J Am Chem Soc       Date:  2004-12-08       Impact factor: 15.419

5.  Homopolymer micelles in heterogeneous solvent mixtures.

Authors:  Subhadeep Basu; Dharma Rao Vutukuri; S Thayumanavan
Journal:  J Am Chem Soc       Date:  2005-12-07       Impact factor: 15.419

6.  Comparison of facially amphiphilic biaryl dendrimers with classical amphiphilic ones using protein surface recognition as the tool.

Authors:  Akamol Klaikherd; Britto S Sandanaraj; Dharma Rao Vutukuri; S Thayumanavan
Journal:  J Am Chem Soc       Date:  2006-07-19       Impact factor: 15.419

7.  The Localization of Guests in Water-Soluble Oligoethyleneoxy-Modified Poly(propylene imine) Dendrimers This work was supported by the Netherlands Foundation for Chemical Research (CW), with financial aid from the Netherlands Organisation for Scientific Research (NWO). The authors thank Stefan Meskers, Harry Dekkers, Marcel van Genderen, and Rint Sijbesma for stimulating discussions. DSM Research is acknowleged for providing the poly(propyleneimine) dendrimers. M.B. and R.K. acknowledge financial support under the TMR/LSF program of the European Union (No. ERBFMGECT980134) to the EMBL Hamburg outstation.

Authors: 
Journal:  Angew Chem Int Ed Engl       Date:  2000-04       Impact factor: 15.336

  7 in total
  5 in total

1.  Smaller building blocks form larger assemblies: aggregation behavior of biaryl-based dendritic facial amphiphiles.

Authors:  Ashootosh V Ambade; Sivakumar V Aathimanikandan; Derek van der Poll; S Thayumanavan
Journal:  J Org Chem       Date:  2007-10-04       Impact factor: 4.354

2.  Synthesis of a pH-independent bifurcated amphiphile.

Authors:  Kaitlin A Willham; Boyd A Laurent; Scott M Grayson
Journal:  Tetrahedron Lett       Date:  2008-03-24       Impact factor: 2.415

3.  Janus-type dendrimer-like poly(ethylene oxide)s.

Authors:  Xiaoshuang Feng; Daniel Taton; Emmanuel Ibarboure; Elliot L Chaikof; Yves Gnanou
Journal:  J Am Chem Soc       Date:  2008-08-06       Impact factor: 15.419

4.  Stimuli Sensitive Amphiphilic Dendrimers.

Authors:  R Rajasekhar Reddy; Krishna R Raghupathi; Diego Amado Torres; S Thayumanavan
Journal:  New J Chem       Date:  2012-02-01       Impact factor: 3.591

5.  Supramolecular disassembly of facially amphiphilic dendrimer assemblies in response to physical, chemical, and biological stimuli.

Authors:  Krishna R Raghupathi; Jing Guo; Oyuntuya Munkhbat; Poornima Rangadurai; S Thayumanavan
Journal:  Acc Chem Res       Date:  2014-06-17       Impact factor: 22.384

  5 in total

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