Structure and reactivity of alkoxycarbonyl (ester)-terminated monolayers on silicon: Sum frequency generation spectroscopy

Journal of Physical Chemistry B

Volumn 110, Issue 10, 2006, Pages 4892-4899

  Asanuma, Hidehiko ^a   Noguchi, Hidenori ^b   Uosaki, Kohei ^b   Yu, Hua Zhong ^a  

^a SIMON FRASER UNIVERSITY   (Canada)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CRYSTALLINE MATERIALS; MONOLAYERS; SEMICONDUCTOR DEVICES; SILICON COMPOUNDS; SPECTROSCOPIC ANALYSIS;

BIOLOGICAL MACROMOLECULES; CARBOXYLIC ACID-TERMINATED MONOLAYERS; SEMICONDUCTOR-BASED BIOSENSING DEVICES;

ESTERS;

EID: 33645519014     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp056131+     Document Type: Article

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61. -; 0, 120, and 240° for nonresonance); the average of the three values was used for calculating the hydrolysis efficiency, while the differences between them were used to calculate the uncertainty.
62. 2 signals. Absolute peak intensities are also affected by variations of the laser intensity during prolonged operation; therefore, a more reliable estimate of the ester hydrolysis efficiency is obtained from the rotational anisotropy data (Figure 6) that takes the NR contribution as the internal reference.