Abstract
The scaling of nuclear spin-dependent parity violating effects with increasing nuclear charge is discussed in two series of isovalent open-shell diatomic molecules. The parameter characterising the strength of parity violation in diatomic molecules is calculated in the framework of the zeroth-order regular approximation (ZORA) and found to be in good agreement with the scaling law derived for atoms in which represents a relativistic enhancement factor. The influence of electron correlation is studied on the molecular level, with spin-polarisation effects being conveniently accounted for by a previously established approximate relation between the hyperfine coupling tensor and . For high accuracy predictions of parity violating effects in radium fluoride the necessity for systematically improvable correlation calculations is emphasised.
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