Natural isotopic abundance: 0.00204.

Reference

[2013Sta]

Method

Continuous wave – cavity ring down spectroscopy.

Equations

Equations 47 and 52 in chapter “Introduction”.

Statistical errors

One standard deviation in units of the least significant full size digit.

Remarks

The integrated intensities are given in units of cm/molecule at 296 K.

Their values correspond to the sum of their individual line intensities, calculated with a cut-off equal to 1 × 10−28 cm/molecule at 296 K.

Dipole transition moment operator constant is given in Debye.

Calculated constants are purposely given with a supplementary digit, in index form, in order to reproduce the line intensities to experimental accuracy.

Spectroscopic parameters are given in chapter “16O18O16O Vibrational Energy and Rotational and Centrifugal Distortion Constants of the (025), (501), and (dark4) Interacting States. Band Centers of the 2ν2 + 5ν3, and 5ν1 + ν3 Bands”.

The isotopic composition of the elements used for the calculation of the natural isotopic abundance is taken from [2007Coh].

Abbreviations

SE: Statistical error.

 

{A,B} = AB + BA

Band

Integrated intensity

Transformed dipole transition moment operator

Parameters

SE

2ν2 + 5ν3

4.69 × 10−24

   

A-type band

 

φZ × 104

0.54029

54

  

{φZ, J2} × 107

−0.4276

75

  

\( \left\{{\varphi}_Z,{J}_Z^2\right\}\times {10}^8 \)

0.3237

86

5ν1 + ν3

3.79 × 10−24

   

A-type band

 

φZ × 104

0.49210

84

Symbols and abbreviations

Short form

Full form

υ 1 υ 2 υ 3

Upper vibrational level in normal mode notation

J x ,J y ,J z

Molecule-fixed components of J

SE

Statistical error