Okamoto, Akiko published the artcileElectrophilic aromatic aroylation polycondensation synthesis of wholly aromatic polyketone composed of 2,2′-dimethoxy-1,1′-binaphthylylene moiety, Computed Properties of 2960-93-2, the publication is Reactive & Functional Polymers (2007), 67(11), 1243-1251, database is CAplus.
A wholly aromatic polyketone containing 2,2′-dimethoxy-1,1′-binaphthylylene moiety was successfully synthesized via electrophilic aromatic aroylation polycondensation with the aid of trifluoromethanesulfonic acid (TfOH) or phosphorus(V) oxide-methanesulfonic acid mixture (P2O5-MsOH). The polycondensation reactions employing two sets of monomers of opposite combination that should afford the same structure of repeating unit showed distinct results. The polycondensation employing 2,2′-dimethoxy-1,1′-binaphthyl (4) as the acyl-acceptant monomer proceeded to give medium-mol.-weight polymer. The polymer synthesis via transformation of biaryl 4 into the corresponding acyl-donor monomer 12 followed by polycondensation with 2,2′-dimethoxybiphenyl (1) predominated the procedure of direct usage of biaryl 4 as the acyl-acceptant monomer. Acyl-acceptant monomer has been demonstrated to play a more crucial role in determination of polymerizability than acyl-donor one.
Reactive & Functional Polymers published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C22H18O2, Computed Properties of 2960-93-2.
Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem