CaltechAUTHORS
  A Caltech Library Service

Anisotropy of Pairwise Interactions between Hexadecanes in Water Measured by AFM Force Spectroscopy

Ray, Chad and Gu, Chao and Brown, Jason R. and Kirkpatrick, Andrea and Akhremitchev, Boris B. (2008) Anisotropy of Pairwise Interactions between Hexadecanes in Water Measured by AFM Force Spectroscopy. Journal of Physical Chemistry C, 112 (46). pp. 18164-18172. ISSN 1932-7447. https://resolver.caltech.edu/CaltechAUTHORS:20161014-160237225

[img] PDF (Detailed description of the data manipulation; all histograms of rupture forces and loading rates) - Supplemental Material
See Usage Policy.

585Kb

Use this Persistent URL to link to this item: https://resolver.caltech.edu/CaltechAUTHORS:20161014-160237225

Abstract

The pulling coordinate dependence of hexadecane dimer dissociation in water was studied using AFM-based single molecule force spectroscopy. Hexadecanes were covalently bound to both the AFM cantilever and to the glass substrates through hydrophilic poly-(ethylene glycol) tethers. The polymer tether was attached either to the end of hexadecane or in the middle of the molecule. Experimentally studied configurations of hexadecanes tethered to the AFM probe and to the glass substrate include a symmetric end-attached configuration (EE), an asymmetric end-attached vs middle-attached configuration (ME), and a symmetric middle-attached configuration (MM). Kinetic parameters of the distance to the transition state barrier (barrier width) and activation energy of dissociation were extracted from the statistical analysis of double tether rupture events. The rupture force analysis employs a recently introduced two-bond model that corrects for errors induced by potential multiple simultaneous rupture events and accounts for the tether stiffening effects. Effects of the shape of intermolecular potential were considered by using the Bell−Evans and Hummer−Szabo force spectroscopy models. The activation energies to dissociation were similar for all configurations while the barrier width was significantly shorter for the MM and ME configurations than for EE configurations. Primitive models that include touching or merging spherical or cylindrical shapes were considered. These models were inconsistent with the extracted kinetic parameters. It is suggested that the observed anisotropy may be a result of conformational transition of hexadecane from extended to collapsed state during dimerization. A flexible four-bead model of hexadecane was introduced to account for conformational flexibility. Using the length and solvent accessible surface area of hexadecane, the four-bead model gave molecular dissociation parameters consistent with the experimental data. This suggests that conformational flexibility is an important factor in hydrophobic interactions between alkane chains.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/jp806580fDOIArticle
http://pubs.acs.org/doi/abs/10.1021/jp806580fPublisherArticle
http://pubs.acs.org/doi/suppl/10.1021/jp806580fPublisherSupporting Information
Additional Information:© 2008 American Chemical Society. Received: July 24, 2008; Revised Manuscript Received: September 11, 2008. Publication Date (Web): October 23, 2008. The authors thank Duke University and NSF Grant No. CHE-0719043 for financial support. The authors also gratefully acknowledge financial support from the ARO (W911NF-04-100191) and Gilbert Walker.
Funders:
Funding AgencyGrant Number
Duke UniversityUNSPECIFIED
NSFCHE-0719043
Army Research Office (ARO)W911NF-04-100191
Gilbert WalkerUNSPECIFIED
Issue or Number:46
Record Number:CaltechAUTHORS:20161014-160237225
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20161014-160237225
Official Citation:Anisotropy of Pairwise Interactions between Hexadecanes in Water Measured by AFM Force Spectroscopy Chad Ray, Chao Gu, Jason R. Brown, Andrea Kirkpatrick, and Boris B. Akhremitchev The Journal of Physical Chemistry C 2008 112 (46), 18164-18172 DOI: 10.1021/jp806580f
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:71126
Collection:CaltechAUTHORS
Deposited By: George Porter
Deposited On:17 Oct 2016 19:40
Last Modified:03 Oct 2019 16:04

Repository Staff Only: item control page