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Presenter

Notes

30 min

Update with fitting to larger hydrocarbon set

View file
nameOpenFF_Gokey_ChemPer_call_2021-01-22.pdf

Trevor

  • new fitting we larger set, ~170 molecules, mainly AlkEtOH

  • Gradients are now an objective, no hessians(?)

  • Rest of procedure is similar as before

  • CBn: Why one conformer per molecule?

  • TG: Molecules are small, that is why only one conformer. Standard settings for conformer generation

  • CBy: What is the purpose of 3-4 Ang cutoff in the conformers?

  • TG: For the simple molecules only small number of molecules came out.

  • CBy: Relative energy differences between conformers are informative. Why only few alkenes, but many alkanes

  • TG: This is what is in the dataset (Alketoh)

  • CBy: The parameters (slide 3) are two categories. One that have enough data, and the ones that don’t.

  • Splitting of a1 is important, same result as last time. It is split multiple times. See slide 4

  • four membered rings seem to drive the splitting here, see splits 4,5,6

  • CBn: Can your method recover something where we exactly know the result?

  • TG: Something I’m working on. Will do later, needs lots of compute.

  • CBy: SMARTS strings representation seems to be very specific for dataset. They will fail badly with other molecules.

  • Looking at “variances” of the parameters.

  • Splitting of a1 reduces number of bits-represented and No. of primitives

  • CBn: Additional parameters will almost always make ff better in the training set. Will be specific for the training set

  • DM: Might try to evaluate FF on validation set during the fit

  • slide 6: not completely clear how the scoring works right now. Needs some more clarification

  • DM: Maybe a small write-up would be helpful

  • TG: Yes, good idea. Was planning to do so.

  • CBy: The amount of possible splits and chemistry is very huge. Can you find common chemistry in splits. Need a way to divide space in an informative way.

  • Next steps: only alkane dataset, make a case where we know the answer and see if we arrive there. Start with one bond and one angle. generally improve experimental design.





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