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• W2913309939 endingPage "4687" @default.
• W2913309939 startingPage "4683" @default.
• W2913309939 abstract "Stable homocarbaporphyrinoids were successfully synthesized by incorporating the m-o-m and p-o-p terphenyl units into the porphyrin core. The distinct bonding modes of terphenyl in the macrocycle generated two structural isomers with two and four carbon atoms in the macrocyclic environment. The core was utilized to stabilize the RhI ion. The spectral and structural analyses revealed that the restricted (m-o-m) and allowed (p-o-p) conjugation in the macrocyclic core provide overall non-aromatic characteristics both to the free bases and their complexes." @default.
• W2913309939 created "2019-02-21" @default.
• W2913309939 creator A5008029974 @default.
• W2913309939 creator A5032719853 @default.
• W2913309939 creator A5083009638 @default.
• W2913309939 creator A5085320347 @default.
• W2913309939 date "2019-03-08" @default.
• W2913309939 modified "2023-10-01" @default.
• W2913309939 title "Homocarbaporphyrinoids: The <i>m‐o‐m</i> and <i>p‐o‐p</i> Terphenyl Embedded Expanded Porphyrin Analogues and Their Rh ^I Complexes" @default.
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• W2913309939 doi "https://doi.org/10.1002/chem.201900495" @default.
• W2913309939 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30715756" @default.
• W2913309939 hasPublicationYear "2019" @default.
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