Ring-opening reaction of a trifluorinated indolylfulgide: mode-specific photochemistry after pre-excitation.

نویسندگان

  • Simone Draxler
  • Thomas Brust
  • Stephan Malkmus
  • Jessica A DiGirolamo
  • Watson J Lees
  • Wolfgang Zinth
  • Markus Braun
چکیده

The ring-opening reaction of a trifluorinated indolylfulgide has been studied as a function of temperature and optical pre-excitation where it was found that reaction times decreased as temperature increased from 10.3 ps at 12 degrees C to 7.6 ps at 60 degrees C. Simultaneously, the quantum yields for the ring-opening reaction grew from 3.1% (12 degrees C) to 5.0% (60 degrees C). When the reaction was started from a non-equilibrium state generated by a directly preceding ring-closure process, the ring-opening reaction became faster and the quantum efficiency increased by more than a factor of three. Analysis of the experimental results points to mode-specific photochemistry in that the promoting, photochemically active modes of the photoreaction are efficiently excited by the directly preceding ring-closure reaction.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ultraschnelle photochemische Reaktionen: Perizyklische Reaktionen photochromer Indolylfulgide und primärer Energietransfer der bakteriellen Photosynthese

In this work several ultrafast photochemical processes are investigated. One focus is the characterisation of the pericyclic reactions of photochromic indolylfulgides and -fulgimides and the exploration of different possibilities to tune these reactions. The second part treats the primary energy and electron transfer steps in the photosynthesis of purple bacteria. All these ultrafast processes ...

متن کامل

Electronically excited states and photochemical reaction mechanisms of β-glucose.

Carbohydrates are important molecular components of living matter. While spectroscopic and computational studies have been performed on carbohydrates in the electronic ground state, the lack of a chromophore complicates the elucidation of the excited-state properties and the photochemistry of this class of compounds. Herein, we report on the first computational investigation of the singlet phot...

متن کامل

New insights in the photochromic spiro-dihydroindolizine/betaine-system.

We have revisited the photochromic spiro-dihydroindolizine/betaine (DHI/B) system applying state-of-the-art density functional theory (DFT) calculations in combination with stationary and time-resolved absorption measurements. DHI/B-systems are becoming increasingly important as potential molecular machines, molecular switches, and photoswitchable electron-acceptors. The knowledge of the exact ...

متن کامل

B-podands as efficient catalysts for the ring opening of epoxides in water: A versatile and atom economical method for the synthesis of vicinal azidoalcohols

For the first time B-podands have been studied as an efficient and powerful catalysts in the ring opening of epoxides with azide anion in water. The reaction afforded the corresponding 1,2-azidoalcohols with high regioselectivity under mild reaction conditions and in a highly atom economic fashion.

متن کامل

B-podands as efficient catalysts for the ring opening of epoxides in water: A versatile and atom economical method for the synthesis of vicinal azidoalcohols

For the first time B-podands have been studied as an efficient and powerful catalysts in the ring opening of epoxides with azide anion in water. The reaction afforded the corresponding 1,2-azidoalcohols with high regioselectivity under mild reaction conditions and in a highly atom economic fashion.

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Physical chemistry chemical physics : PCCP

دوره 11 25  شماره 

صفحات  -

تاریخ انتشار 2009