Literature DB >> 25686771

Cycloalkyl-aminomethylrhodamines: pH dependent photophysical properties tuned by cycloalkane ring size.

Chuangjun Liu1, Quinn A Best, Brian Suarez, Jack Pertile, Matthew E McCarroll, Colleen N Scott.   

Abstract

A series of fluorescent pH probes based on the spiro-cyclic rhodamine core, n class="Chemical">aminomethylrhodamines (AMR), was synthesized and the effect of cycloalkane ring size on the acid/base properties of the AMR system was explored. The study involved a series of rhodamine 6G (cAMR6G) and rhodamine B (cAMR) pH probes with cycloalkane ring sizes from C-3 to C-6 on the spiro-cyclic amino group. It is known that the pKa value of cycloalkylamines can be tuned by different ring sizes in accordance with the Baeyer ring strain theory. Smaller ring amines have lower pKa value, i.e., they are less basic, such that the relative order in cycloalkylamine basicity is: cyclohexyl > cyclopentyl > cyclobutyl > cyclopropyl. Herein, it was found that the pKa values of the cAMR and cAMR6G systems can also be predicted by Baeyer ring strain theory. The pKa values for the cAMR6G series were shown to be higher than the cAMR series by a value of approximately 1.

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Year:  2015        PMID: 25686771      PMCID: PMC4396821          DOI: 10.1007/s10895-015-1519-z

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  11 in total

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8.  Anilinomethylrhodamines: pH sensitive probes with tunable photophysical properties by substituent effect.

Authors:  Quinn A Best; Chuangjun Liu; Paul D van Hoveln; Matthew E McCarroll; Colleen N Scott
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  1 in total

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  1 in total

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