TY - JOUR

T1 - Microwave measurements and ab initio calculations of structural and electronic properties of N -Et-1,2-azaborine

AU - Tanjaroon, Chakree

AU - Daly, Adam

AU - Marwitz, Adam J.V.

AU - Liu, Shih Yuan

AU - Kukolich, Stephen

N1 - Funding Information:
This material is based upon work supported by the National Science Foundation under Grant Nos. CHE-0721505 and CHE-0809053. We are very grateful to the NSF for providing funding for this research. We thank Laszlo Sarkozy for the development of a new spectral analysis program which aided in finding weak transitons.

PY - 2009

Y1 - 2009

N2 - Rotational transitions for N -Et-1,2-azaborine were measured in the 5-13 GHz range using a Flygare-Balle type Fourier transform spectrometer system. Twelve distinct rotational transitions with over 130 resolved hyperfine components, which included a-dipole and b-dipole transitions, were measured and analyzed to obtain rotational constants and 11B and 14N nuclear quadrupole coupling constants in the principal rotational axis system. Rotational constants obtained are A=4477.987(4), B=1490.5083(7), and C=1230.6728(6) MHz. The quadrupole coupling constants for 11B are eQqaa=-1.82(1), (eQqbb-eQqcc)=-3.398 (4) MHz, and for 14N, eQqaa=1.25(1), (eQqbb-eQq cc)=0.662(4) MHz. Quantum electronic structure calculations predict a ground-state structure with the ethyl group perpendicular to the azaborine plane and rotational constants in very good agreement with the measured structure and rotational constants. The theoretical conformational analysis of the ethyl group rotation around the N-C bond in relation to the heterocyclic ring yielded an asymmetric torsional potential energy surface with barrier heights of about 900 and 1350 cm-1 for the N-Et-1,2-zaborine. Results of the measurements and calculations indicate that the basic molecular structure of N-Et-1,2-azaborine is similar to ethylbenzene. Electrostatic potential calculations qualitatively show that π-electron density is somewhat delocalized around the 1,2-azaborine ring.

AB - Rotational transitions for N -Et-1,2-azaborine were measured in the 5-13 GHz range using a Flygare-Balle type Fourier transform spectrometer system. Twelve distinct rotational transitions with over 130 resolved hyperfine components, which included a-dipole and b-dipole transitions, were measured and analyzed to obtain rotational constants and 11B and 14N nuclear quadrupole coupling constants in the principal rotational axis system. Rotational constants obtained are A=4477.987(4), B=1490.5083(7), and C=1230.6728(6) MHz. The quadrupole coupling constants for 11B are eQqaa=-1.82(1), (eQqbb-eQqcc)=-3.398 (4) MHz, and for 14N, eQqaa=1.25(1), (eQqbb-eQq cc)=0.662(4) MHz. Quantum electronic structure calculations predict a ground-state structure with the ethyl group perpendicular to the azaborine plane and rotational constants in very good agreement with the measured structure and rotational constants. The theoretical conformational analysis of the ethyl group rotation around the N-C bond in relation to the heterocyclic ring yielded an asymmetric torsional potential energy surface with barrier heights of about 900 and 1350 cm-1 for the N-Et-1,2-zaborine. Results of the measurements and calculations indicate that the basic molecular structure of N-Et-1,2-azaborine is similar to ethylbenzene. Electrostatic potential calculations qualitatively show that π-electron density is somewhat delocalized around the 1,2-azaborine ring.

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U2 - 10.1063/1.3270157

DO - 10.1063/1.3270157

M3 - Article

C2 - 20001041

AN - SCOPUS:72449155544

VL - 131

JO - Journal of Chemical Physics

JF - Journal of Chemical Physics

SN - 0021-9606

IS - 22

M1 - 224312

ER -