Dear Naeimeh Hassanzadeh Goji apparently yes. At least I found this potentially useful article in which reactions of porphyrins with certain halogenated carboxylic acids is reported. The article is entitled

Noncovalent interactions in acid–porphyrin complexes

https://pubs.rsc.org/en/content/articlelanding/2012/sc/c2sc20271a#!divAbstract

Hi Naeimeh Hassanzadeh Goji

You can see porphyrin crystal structures where strong carboxylic acids located in top and down porphyrin macrocycle and undergoing very strong Hydrogen bonding. In this paper (Article Structural elucidation and study of intermolecular interacti...

In another paper ( https://pubs.rsc.org/en/content/articlehtml/2015/ra/c5ra18310c ) where we used explosive picric acid and we observed the same phenomenon. Picric acid hydrogenating porphyrin core and undergoing strong interaction don't expect any other reactions with core nitrogen

acid–porphyrin complexation is shown to be compatible with established metal–ligand interactions in the generation of novel supramolecular assemblies in solution.

Article Nitrogen atom activation: The influence of porphyrin ring st...

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Frank T. Edelmann

Sorry for delay Dear Professor and Thanks for your precious Answers

In fact, I'm looking for a way to have a H bonding between N in Porphyrin ring and a carboxylic acid-functionalized polymer,

I have no idea if It's possible considering weak protonation ability of carboxylic end in comparison to haloganated acids..

dear Rahul Soman ! Thanks for your answer,

As I see, both of these Acids You mentioned, have electron-withdrawing groups, and are able to protonate Nitrogen atoms, Did you Try any weak acid also?

I read somewhere that Porphyrins are acid sensitive..don't they decompose in this conditions?

Naeimeh Hassanzadeh Goji tetraphenyl porphyrin derivatives are not that much acid sensitive. it won't degrade quickly. I tried weak acids but not successful in getting single crystals.

https://www.researchgate.net/profile/Rahul-Soman-2

Thanks!