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This just not works and there are\n profound reasons behind...hence this update would never be merged to\n master and will stay here as a memento.\n\nWhat I mean?\n\n> if I apply a SSR to the total bond correlation, which is a mutual info\n I could naively expect that, given MI = 2S1 - S2, the SSR would give:\n\n MI|SSR = 2 * S1|SSR - S2|SSR\n\n This notation is truly misleading and could lead to severe paradoxes,\n like thinking that SSR and algebraic operations do not commute.\n\nHow is this solved?\n\n> changing how we phrase and write the terms, i.e. we can write\n\n MI|SSR = 2 * S1|SSR - S2|SSR\n\n but we need to make sure to understand that S1|SSR is NOT the local\n entanglement and S2|SSR the quasilocal entanglement under the SSR.\n\n————————————————————————————————————————————————————————————————————————\n\nLET'S CLARIFY THE CONCEPT...\n\nElaborating a bit I believe we may want to keep a clear cut between the\nmathematical and the physical names.\n\n- Von Neumann entropies and mutual information are mathematical objects,\n and the latter is defined in terms for the former.\n\n- Local (and quasilocal) entanglement and total correlation are physical\n quantities, that happen to correspond to one mathematical object under\n some assumptions, but to some other thing under other assumptions.\n\nWithout SSRs everything is simple cause the (quasi)local entanglement is\ngiven by the relevant von Neumann entropies of the relevant RDMs and the\ntotal correlation is the mutual information between two orbitals, hence\nwe have additivity in the sense that the total correlation comes from an\nalgebraic sum of local and quasilocal entanglement.\n\nWith SSRs there's care to be taken since local & quasilocal entanglement\nare not von Neumann entropies, yet the total correlation is still defined\nas a mutual information, acting on a filtered RDM.\nHence it comes from an algebraic sum of von Neumann entropies, but not of\nentanglement measures, since they are not von Neumann entropies.\n\n—————————————————————————————————————————————————————————————————————————\n\nLET'S TRY TO FIND AN IMPROVED NOTATION THEN...\n\nSo, let's call E1 the measure of entanglement between a single site and\nthe whole. S1 is instead just the mathematical definition of von Neumann\nentropy of the RDM1 (same for E2, S2 and RDM2 for the dimer quantities,\ninstead of single site).\n\nWhithout SSRs we have that E1 = S1, E2 = S2 and MI = 2S1 - S2, hence the\nalgebra works fine cause you literally have MI == 2E1 - E2.\n\nBut with SSRs it's not true that E1 = S1 and E2 = S2.\nFor E2 I'm not sure, we would need to derive something following the\nideas in that JCTC for the dimer case.\nBut for E1 the formula is definitely not S1|{SSR on the RDM1}.\nIt is a completely different formula than the von Neumann entropy acting\non the untouched RDM for the single site.\nIt can be derived of course as coming from imposing the SSR on the whole\nDM, but this is irrelavant here.\n\nThat's why when you compute MI with the SSR you do something to the RDM2\nand then get some S1|SSR and S2|SSR to plug in the MI|SSR formula, but\nyou don't have additivity with E1|SSR and E2|SSR, cause these two aren't\nvon Neumann entropies anymore.\nWhy the dimer and single site entanglement are not von Neumann entropies\nanymore? Because applying SSRs to the whole DM you make it in general an\nimpure state and von Neumann entropies of its reduced systems are not\nmeasures of entanglement anymore.\n\n————————————————————————————————————————————————————————————————————————\n\nFINALLY A COMMENT ON WHY S1|SSR IS EXACTLY THE SAME AS S1\n\nThis is another source of confusion... S2|SSR is different from S2, but\nnot a correct expression for E2|SSR, ok. Further, while we know there is\nan inequality associated to the SSRs (E2|SSR ≤ E2) this is not valid for\nS2 and S2|SSR.\n\nBut having S1|SSR == S1 can become even more confusing... we are doing a\nrestriction on the RDM2 and this leads to a different S2, but how can it\nleave unchanged S1, a functional of RDM1, which is a trace of RDM2?\n\nHere my best (technical) answer:\n\n We know SSRs are local. Hence each local N or parity has to be\n conserved. When we trace from either an untouched or SSR RDM2,\n we need to keep the \"to be traced site\" state fixed. 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