Abstract

The emission transition dipole moments of single-molecule free-base phthalocyanines at an air/glass interface were visualized using defocused wide-field fluorescence microscopy at a temporal resolution of 100-200 ms. Isolated molecules showed slow proton tautomerization, which is consistent with previous theoretical calculations in the gas phase, which predicted large activation energies.

Highlights

  • (B100 s) compared with the rate of tautomerization

  • Isolated molecules showed slow proton tautomerization, which is consistent with previous theoretical calculations in the gas phase, which predicted large activation energies

  • We report the real-time visualization of the ETDMs of single H2Pcs using defocused wide-field microscopy at a temporal resolution of 100 ms.[18,19,20,21,22,23]

Read more

Summary

Introduction

(B100 s) compared with the rate of tautomerization. In this study, we report the real-time visualization of the ETDMs of single H2Pcs using defocused wide-field microscopy at a temporal resolution of 100 ms.[18,19,20,21,22,23] We found that a H2Pc derivative shows slow tautomerization at an air/octadecyl-group-modified glass interface, which is consistent with previous DFT calculations. ISSN 1359-7345 COMMUNICATION Hiroyuki Noji et al Real-time fluorescence visualization of slow tautomerization of single free-base phthalocyanines under ambient conditions Real-time fluorescence visualization of slow tautomerization of single free-base phthalocyanines under ambient conditions†‡

Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.