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- W2574311426 abstract "Abstract Carbatriphyrin(3.1.1) is the structural isomer of biphenylcorrole and achieved by switching the bonding mode of biphenyl unit from 3,3′ to 2,3′ which turns the corrole into a triphyrin analogue. The presence of a m ‐arene unit in the framework restricts the overall conjugation and thus leads to a nonaromatic macrocycle. The protonation experiments afford a trifluoroacetate ion complex. The coordination chemistry reveals that the bottom approach of boron(III) ion forms weak C−H⋅⋅⋅B interactions, however a top approach stabilizes the organoborane complex and the product distribution relies on the basicity of the proton scavengers. These results are unambiguously confirmed by single‐crystal X‐ray analyses." @default.
- W2574311426 created "2017-01-26" @default.
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- W2574311426 creator A5081952488 @default.
- W2574311426 creator A5085320347 @default.
- W2574311426 date "2017-02-14" @default.
- W2574311426 modified "2023-10-16" @default.
- W2574311426 title "Carbatriphyrin(3.1.1)-A Distinct Coordination Approach of B<sup>III</sup> to Generate Organoborane and Weak C−H⋅⋅⋅B Interactions" @default.
- W2574311426 cites W1846858789 @default.
- W2574311426 cites W1915398327 @default.
- W2574311426 cites W1915453845 @default.
- W2574311426 cites W1976676084 @default.
- W2574311426 cites W1978850019 @default.
- W2574311426 cites W1991481512 @default.
- W2574311426 cites W1992074545 @default.
- W2574311426 cites W1999403499 @default.
- W2574311426 cites W2004145702 @default.
- W2574311426 cites W2004980486 @default.
- W2574311426 cites W2007709651 @default.
- W2574311426 cites W2009529986 @default.
- W2574311426 cites W2011781503 @default.
- W2574311426 cites W2017024750 @default.
- W2574311426 cites W2017580294 @default.
- W2574311426 cites W2026742872 @default.
- W2574311426 cites W2037870884 @default.
- W2574311426 cites W2037905458 @default.
- W2574311426 cites W2038079583 @default.
- W2574311426 cites W2039571723 @default.
- W2574311426 cites W2042239958 @default.
- W2574311426 cites W2047027124 @default.
- W2574311426 cites W2055910958 @default.
- W2574311426 cites W2057562352 @default.
- W2574311426 cites W2062488673 @default.
- W2574311426 cites W2070304736 @default.
- W2574311426 cites W2070797924 @default.
- W2574311426 cites W2072104136 @default.
- W2574311426 cites W2074059728 @default.
- W2574311426 cites W2080745068 @default.
- W2574311426 cites W2086919086 @default.
- W2574311426 cites W2087395600 @default.
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- W2574311426 cites W2112373670 @default.
- W2574311426 cites W2113919180 @default.
- W2574311426 cites W2117851140 @default.
- W2574311426 cites W2118641701 @default.
- W2574311426 cites W2122746064 @default.
- W2574311426 cites W2125384750 @default.
- W2574311426 cites W2133205554 @default.
- W2574311426 cites W2135034266 @default.
- W2574311426 cites W2138979752 @default.
- W2574311426 cites W2143877952 @default.
- W2574311426 cites W2144821086 @default.
- W2574311426 cites W2147754111 @default.
- W2574311426 cites W2148517659 @default.
- W2574311426 cites W2150518729 @default.
- W2574311426 cites W2159136536 @default.
- W2574311426 cites W2165181332 @default.
- W2574311426 cites W2167344739 @default.
- W2574311426 cites W2168779290 @default.
- W2574311426 cites W2171596556 @default.
- W2574311426 cites W2184258549 @default.
- W2574311426 cites W2195366495 @default.
- W2574311426 cites W2264178839 @default.
- W2574311426 cites W2288565508 @default.
- W2574311426 cites W2291182811 @default.
- W2574311426 cites W2314193242 @default.
- W2574311426 cites W2317621835 @default.
- W2574311426 cites W2317638461 @default.
- W2574311426 cites W2326633903 @default.
- W2574311426 cites W2329106886 @default.
- W2574311426 cites W2329424602 @default.
- W2574311426 cites W2415855715 @default.
- W2574311426 cites W2949615918 @default.
- W2574311426 cites W4210336194 @default.
- W2574311426 cites W4230479053 @default.
- W2574311426 cites W4232705977 @default.
- W2574311426 cites W4233660688 @default.
- W2574311426 cites W4233886515 @default.
- W2574311426 cites W4234282022 @default.
- W2574311426 cites W4234472203 @default.
- W2574311426 cites W4234613543 @default.
- W2574311426 cites W4237692357 @default.
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- W2574311426 cites W4250992989 @default.
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- W2574311426 cites W4361867951 @default.
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- W2574311426 doi "https://doi.org/10.1002/chem.201605332" @default.
- W2574311426 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28106933" @default.
- W2574311426 hasPublicationYear "2017" @default.
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