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| Main Authors: | , |
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| Format: | Preprint |
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2024
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| Online Access: | https://arxiv.org/abs/2409.03994 |
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| _version_ | 1866912017262051328 |
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| author | Ireland, Robbie T. McKemmish, Laura K. |
| author_facet | Ireland, Robbie T. McKemmish, Laura K. |
| contents | Despite the fact that most quantum chemistry basis sets are designed for accurately modelling valence chemistry, these general-purpose basis sets continue to be widely used to model core-dependent properties. Core-specialised basis sets are designed with specific features to accurately represent the behaviour of the core region. This design typically incorporates Gaussian primitives with higher exponents to capture core behaviour effectively, as well as some decontraction of basis functions to provide flexibility in describing the core electronic wave function. The highest Gaussian exponent and the degree of contraction for both $s$- and $p$-basis functions effectively characterise these design aspects.
In this study, we compare the design and performance of general-purpose basis sets against several literature basis sets specifically designed for three core-dependent properties: J coupling constants, hyperfine coupling constants, and magnetic shielding constants (used for calculating chemical shifts). Our findings consistently demonstrate a significant reduction in error when employing core-specialised basis sets, often at a marginal increase in computational cost compared to the popular 6-31G** basis set. Notably, for expedient calculations of J coupling, hyperfine coupling and magnetic shielding constants, we recommend the use of the pcJ-1, EPR-II, and pcSseg-1, basis sets respectively. For higher accuracy, the pcJ-2, EPR-III, and pcSseg-2 basis sets are recommended. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2409_03994 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | On the Specialisation of Gaussian Basis Sets for Core-Dependent Properties Ireland, Robbie T. McKemmish, Laura K. Chemical Physics Despite the fact that most quantum chemistry basis sets are designed for accurately modelling valence chemistry, these general-purpose basis sets continue to be widely used to model core-dependent properties. Core-specialised basis sets are designed with specific features to accurately represent the behaviour of the core region. This design typically incorporates Gaussian primitives with higher exponents to capture core behaviour effectively, as well as some decontraction of basis functions to provide flexibility in describing the core electronic wave function. The highest Gaussian exponent and the degree of contraction for both $s$- and $p$-basis functions effectively characterise these design aspects. In this study, we compare the design and performance of general-purpose basis sets against several literature basis sets specifically designed for three core-dependent properties: J coupling constants, hyperfine coupling constants, and magnetic shielding constants (used for calculating chemical shifts). Our findings consistently demonstrate a significant reduction in error when employing core-specialised basis sets, often at a marginal increase in computational cost compared to the popular 6-31G** basis set. Notably, for expedient calculations of J coupling, hyperfine coupling and magnetic shielding constants, we recommend the use of the pcJ-1, EPR-II, and pcSseg-1, basis sets respectively. For higher accuracy, the pcJ-2, EPR-III, and pcSseg-2 basis sets are recommended. |
| title | On the Specialisation of Gaussian Basis Sets for Core-Dependent Properties |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2409.03994 |