4.7 Article

Loading Phlorins with Fullerenes by a [4+2]-Cycloaddition Reaction: Regulation of the Regioselectivity by Pyrrole Linkage Modes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 87, Issue 5, Pages 2758-2766

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c02676

Keywords

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Funding

  1. National Natural Science Foundation of China [NSFC 22108078, 22131005, 21808156, 21971063, 22075077]
  2. Natural Science Foundation of Shanghai [20ZR1414100]
  3. Program of Shanghai Academic Research Leader [20XD1401400]
  4. Fundamental Research Funds for the Central Universities

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Sulfolenopyrrole-based normal and N-confused phlorins were constructed to study the effect of pyrrole linkage modes on the [4 + 2] cycloaddition reaction. The results showed that the confused pyrrole in the N-confused phlorin enabled the rapid formation of a monofullerenoadduct under milder conditions, while the analysis of its structure indicated that fullerene attached to the iminopyrrole part. The high regioselectivity in the [4 + 2] cycloaddition of the imino-type sulfolenopyrrole unit was also supported by density functional theory calculations.
Sulfolenopyrrole-based normal and N-confused phlorins have been constructed to address the seldom touched phlorin functionalization and simultaneously explore the effect of the pyrrole linkage modes (alpha alpha, alpha beta) on the [4 + 2] cycloaddition reaction. The common sulfolenophlorin 1 contains two sulfoleno-pyrroles with the same reactivity upon tautomerization and undergoes stepwise [4 + 2]-cycloaddition with fullerene to furnish monoadduct 1-C60 and bisadduct 1-2C60 with a total yield up to 76%. By contrast, the presence of the confused pyrrole in 2 fixes the Jr-system owing to the low tendency to tautomerize and enables the two sulfolenopyrroles to exhibit in different fashions (i.e., normal NH-type and imino-type). Notably, under milder conditions (120 degrees C), the monofullerenoadduct 2-C60 forms rapidly and has been isolated from the [4 + 2] cycloaddition reaction of 2 and fullerene as the predominant fraction, accompanied by a trace amount of bisadduct 2-2C60. Raising the temperature to 140 degrees C did not improve the yield of 2-2C60. The structural analysis of 2-C60 indicates the attachment of fullerene at the iminopyrrole part. The high regioselectivity in the [4 + 2] cycloaddition of the imino-type sulfolenopyrrole unit has been rationalized thermodynamically by the DFT calculation on the relative energy of the two diene intermediates.

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