Acceleration of a ground-state reaction by selective femtosecond-infrared-laser-pulse excitation

Abstract

Infrared (IR) excitation of vibrations that participate in the reaction coordinate of an otherwise thermally driven chemical reaction are believed to lead to its acceleration. Attempts at the practical realization of this concept have been hampered so far by competing processes leading to sample heating. Here we demonstrate, using femtosecond IR-pump IR-probe experiments, the acceleration of urethane and polyurethane formation due to vibrational excitation of the reactants for 1:1 mixtures of phenylisocyanate and cyclohexanol, and toluene-2,4-diisocyanate and 2,2,2-trichloroethane-1,1-diol, respectively. We measured reaction rate changes upon selective vibrational excitation with negligible heating of the sample and observed an increase of the reaction rate up to 24%. The observation is rationalized using reactant and transition-state structures obtained from quantum chemical calculations. We subsequently used IR-driven reaction acceleration to write a polyurethane square on sample windows using a femtosecond IR pulse.

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Figure 1
Figure 2: Energetics (in kcal mol−1) and geometries for the reaction of PHI with CH-ol in THF for reactant R1, R2, the TS and product CC.
Figure 3: IR absorbance changes with time after mixing PHI and CH-ol without illumination (black lines) and with laser excitation at 3,500 cm−1 (red lines) for times at 0 and 300 min, PHI and CH-ol at 0.75 M, and 0.1 mm sample thickness.
Figure 4: Absorbance difference spectra averaged with respect to selected delay time intervals upon excitation of CH-ol ν(OH) at about 3,500 cm−1 of a 1:1 mixture of CH-ol and PHI in THF.
Figure 5: Polyurethane square generated with IR excitation of a TDI and TCD solution at 2,270 cm−1 due to IR-pulse-induced reaction acceleration.

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Acknowledgements

The work was supported by the Deutsche Forschungsgemeinschaft (grants nos Ku952/6 and He5206/3, CRC 1078 ‘Protonation Dynamics in Protein Function’, Project B07, CRC 1114 ‘Scaling Cascades in Complex Systems’, Project B05). The authors thank N.P. Ernsting for discussions and the group of S. Reich for Raman microscopy experiments.

Author information

T.S. performed the femtosecond experiments on CH-ol and PHI, analysed the data and contributed to writing the paper. Y.Y. performed the femtosecond experiments on CH-ol and PHI. V.K. performed acceleration measurements, photolithography measurements, analysed the data and contributed to writing the paper. F.K. provided the samples. A.A.A. performed the quantum chemical calculations, analysed their results and contributed to writing the paper. K.H. and O.K. contributed to all measurements, calculations and analysis and wrote the paper. All authors commented on the manuscript.

Correspondence to Karsten Heyne.

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Competing interests

V.K., F.K. and K.H. are listed as inventors on a patent application describing infrared-light-induced yield optimization of chemical reactions. These patents are pending in the EU (EP2014056220) and the USA (US 2016/0051963). K.H. is also listed on a patent describing a method for polymerizing monomer units and/or oligomer units by means of infrared light pulses. This patent includes US patent no. 1412448 and EU patent no. EP 2718005. The other authors declare no competing financial interests.

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Stensitzki, T., Yang, Y., Kozich, V. et al. Acceleration of a ground-state reaction by selective femtosecond-infrared-laser-pulse excitation. Nature Chem 10, 126–131 (2018). https://doi.org/10.1038/nchem.2909

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