Femtosecond dynamics of dative bonding: concepts of reversible and dissociative electron transfer reactions.

نویسندگان

  • D Zhong
  • A H Zewail
چکیده

With fs time, speed, and angular resolution of the elementary steps in electron transfer reactions, we report direct observation of reversible and dissociative processes for dative bonding involving covalent and ionic characters. For bimolecular reactions of various donors and acceptors we find strong correlation between the structure and the dynamics. The dynamics from the transition state to final products involve two elementary processes, with different reaction times, speed, and angular distributions. For example, for the R2S.I2 (R = C2H5) system, it is shown that after charge separation, the reversible electron transfer occurs in less than 150 fs (fastest trajectory) and is followed by the rupture of the I-I bond with the release of the first I-atom in 510 fs. However, the second process of the remaining and trapped I-atom takes 1.15 ps with its speed (500 m/s) being much smaller than the first one (1,030 m/s). The S-I-I average angle is 130 degrees. These findings, on this and the other systems reported here, elucidate the mechanism and address some concepts of nonconcertedness, caging, and restricted energy redistribution.

برای دانلود 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

Electrochemical and theoretical analysis of the reactivity of shikonin derivatives: dissociative electron transfer in esterified compounds.

An electrochemical and theoretical analysis of a series of shikonin derivatives in aprotic media is presented. Results showed that the first electrochemical reduction signal is a reversible monoelectronic transfer, generating a stable semiquinone intermediate; the corresponding E(I)⁰ values were correlated with calculated values of electroaccepting power (ω(+)) and adiabatic electron affinities...

متن کامل

Modeling of Reversible Chain Transfer Catalyzed Polymerization by Moment Equations Method

A moment equations method was performed to study the Reversible chain Transfer Catalyzed Polymerization (RTCP) of styrene in 80°C. To do this, a kinetic scheme containing conventional free radical polymerization reactions and equilibrium reactions of RTCP was assumed. After obtaining mass balance equations, three moment equations were defined for free and dormant radicals and dead chains. M...

متن کامل

Interplay of reversible chain transfer and comonomer incorporation reactions in coordination copolymerization of ethylene/1–hexene

Coordinative chain transfer polymerization (CCTP) has opened a new path for the development of novel products like olefin block copolymers and chain-end functional polyolefins. However, conflicting results are frequently reported on the catalyst performance including activity and comonomer selectivity under CCTP conditions. Here we have selected two catalysts including rac-ethylenebis(1-η5-inde...

متن کامل

Electron-transfer reactions of halogenated electrophiles: a different look into the nature of halogen bonding.

The rates of oxidation of ferrocene derivatives by brominated molecules R-Br (CBr3CN, CBr4, CBr3NO2, CBr3COCBr3, CBr3CONH2, CBr3F, and CBr3H) were consistent with the predictions of the outer-sphere dissociative electron-transfer theory. The similar redox-reactions of the R-Br electrophiles with the typical halogen-bond acceptors tetramethyl-p-phenylenediamine (TMPD) or iodide were much faster ...

متن کامل

Ab Initio Quantum-Mechanical Study of the Stability of Cyclic R-Acetoxy-N-nitrosamines: Amine NfNO Dative Bonding in R-Hydroxy-N-nitrosamines Versus NfCarbocation Dative Bonding in N-Nitrosiminium Ions

The dissociations of R-hydroxy-N-nitrosopyrrolidine, 1, and R-hydroxy-N-nitrosopiperidine, 2, to form the nitrosiminium ions, 3 and 4, respectively, have been studied as models for the SN1 process of the corresponding R-acetoxy-N-nitrosamines. In excellent agreement with experiments, the ionization of the pyrrolidine derivative is found to be more endothermic at ab initio levels up to MP4(SDTQ)...

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

برای دانلود 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

عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 96 6  شماره 

صفحات  -

تاریخ انتشار 1999