Hi Chris,

Using the single-scattering and multiple-scattering paths that have the same 
scattering atoms is not double counting. In general, including all the paths 
from a Feff calculation is what you ought to do to account for all of the 
EXAFS.  But many paths will have weak contributions, and so can often be 
neglected.

It gets more tricky to avoid double-counting if you mix paths from multiple 
Feff calculations, but it sounds like that is not what you're doing.

Cheers,

--Matt


________________________________
From: Ifeffit <ifeffit-boun...@millenia.cars.aps.anl.gov> on behalf of Chris 
Pollock <cjp...@cornell.edu>
Sent: Tuesday, April 2, 2024 6:18 PM
To: XAFS Analysis using Ifeffit <Ifeffit@millenia.cars.aps.anl.gov>
Subject: [Ifeffit] Imidazole multiple scattering in Artemis

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Hi everyone,
I've been using Artremis for quite a while, but have only recently come across 
a case where the inclusion of multiple scattering seems to be important for 
fitting some data and wanted to ask what is probably a super basic question to 
make sure I don't mess anything up.

I've recently collected some data on a metalloenzyme with a quite 
histidine-rich active site and, since it's been shown previously that multiple 
scattering is important for fitting the longer range scattering for these types 
of systems, I wanted to make sure I capture this in my Artemis fits.  The data 
appear to show scattering contributions from N3, C2, and N1 in the imidazole 
ring, and FEFF seems to agree that those paths are the most important, though 
it calculates the MS intensity to be significantly greater than the single 
scattering for the farther N (N1).  So, my super naive question is:  To include 
multiple scattering paths in the fits--say, the Fe-N3-N1 triangle--is it 
correct to include the Fe-N3-N1 multiple scattering path in addition to the 
Fe-N3 and Fe-N1 single scattering paths, or would that effectively be double 
counting the farther nitrogen (N1)?

Thanks in advance!
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