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Pillararene

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Ring molecule able to store other molecules within itself

Pillararenes are macrocycles composed of hydroquinone or dialkoxybenzene units (5 to 10) linked in the para position by methylene bridges. They are structurally similar to the cucurbiturils and calixarenes that play an important part in host–guest chemistry. The first pillararene was the five membered dimethoxypillararene.

Chemical structure of pillararene

History

1,4-Dimethoxypillararene, the first pillararene, was reported in 2008 by Tomoki Ogoshi et al. They catalyzed the condensation of 1,4-dimethoxybenzene and paraformaldehyde using a Lewis acid to obtain 1,4-dimethoxypillararene (DMpillararene). The methoxy groups of DMpillararene were then deprotected using boron tribromide and removed to give pillararene. Ogoshi and Kanai decided naming the new family of host macrocycles "pillararene", since they are cylindrical or pillar-like in shape and composed of aromatic or "arene" moieties. Chemists often refer to them as "pillarenes" orally as this is easier to pronounce and remember. It is pertinent to mention that Rathore and Kochi first observed pillararenes in 1995, but were unable to characterize, and reported as a polymer-like material being formed along with diarylmethanes during the transformation of bis(methoxymethyl)-p-hydroquinone ether.

Structure

Pillararenes are composed of hydroquinone units linked by methylene bridges at para-positions. It features a symmetrical pillar architecture with two identical cavity gates. Pillararene is the most conformationally stable member in this family. Due to the close proximity of many electron-rich hydroquinones, the cavity of pillararenes are able to form strong association complexes with electron-poor species. Also, derivatives of the pillararenes can be generated by modifying the hydroxyl groups at all positions or selectively on one or two positions.

Planar chirality

Enantiomers of Pillararene

The orientation of the hydroquinone oxygens on both rims of the pillararene allow the macrocycle to exhibit planar chirality. When the substituent on the hydroquinone oxygen is small enough to fit through the cavity of the pillararene, allowing for oxygen-through-the-annulus rotation to occur, racemization occurs. If this substituent is large enough to prevent rotation, optically active pillararene macrocycles can be isolated.

Assignment of the absolute stereochemical designation of one hydroquinone unit of planar chiral DMpillararene. The pilot atom is shown in purple, and the three atoms used to assign the absolute stereochemistry are labeled and shown as spheres.

A pillararene macrocycle, with n hydroquinone units, has n planes of chirality. DMpillararene has five planes of chirality which are "in sync" in the lowest energy conformational isomer due to unfavorable steric interactions between the methoxy groups of neighboring 1,4-dimethoxy-phenylene units. The absolute stereochemical designation of these planes of chirality in pillararene structures can be assigned following modified Cahn-Ingold-Prelog priority rules. The pilot atom for one of the five planes of chirality in pillararene is assigned to the highest priority atom that is not in the chiral plane - the first carbon atom of the neighboring phenylene unit. The three adjacent in-plane atoms are then assigned, starting with the methylene carbon attached to the pilot atom as priority 1, and the directly connected phenylene carbon as 2, and the carbon atom connected to the methoxy group as 3. When viewed from the side of the pilot atom, if the three atoms form a clockwise direction when followed in order of priority, the molecule is assigned as R(p), otherwise it is assigned as S(p).

Synthesis

Homopillararenes

Three strategies are mainly used to obtain pillararenes (Scheme 1). All of three strategies use an acid as catalyst.

  1. The Lewis acid or trifluoromethanesulfonic acid catalyzed condensation of 1,4-dialkoxybenzene and paraformaldehyde at room temperature.
  2. The condensation of 1,4-dialkoxy-2,5bis(alkoxymethyl)benzene catalyzed by p-toluenesulfonic acid.
  3. Cyclooligomerization of 2,5-dialkoxybenzyl alcohols or 2,5-dialkoxybenzyl bromides with an appropriate Lewis acid as the catalyst.

Copillararenes

In 2010, Feihe Huang et al. introduced three new ways to synthesize copillararenes, which are composed of different repeating units. It is easier to selectively functionalize copillararenes, helping to generate interesting physical properties, conformations, and host–guest binding interactions. There are two possible ways to make copillararenes: to selectively modify repeating monomers of homopillararenes, or to use two different monomers to carry out co-oligomerization.

Mechanism

Pillararenes are traditionally formed through a thermodynamically controlled Friedel-Crafts cyclooligomerization. A practical and effective trifluoromethanesulfonic acid (TfOH)-catalyzed cyclooligomerization strategy was also developed for the synthesis of functionalized pillararenes and copillararenes from 1,4-dialkoxybenzenes with paraformaldehyde under mild reaction conditions, and the reaction mechanism of solution-phase catalytic synthesis of pillararenes was investigated by room-temperature X-band ESR spectroscopy, mass spectroscopy, NMR and control experiments, suggesting a free radical process initially and a Friedel–Crafts alkylation process during the consequent coupling and ring-closure stage.

Selective Synthesis of Pillararene

Pillararene can be targeted as the major product of the Friedel-Crafts cyclooligomerization by using bulky alkoxy groups on the monomer, switching the Lewis acid catalyst or by using a bulky chlorinated solvent. Ogoshi and coworkers reported the synthesis of a pillararene with 1,4-Bis(methylcyclohexyl ether)phenylene units in an 87% yield by using chlorocyclohexane as the solvent. The bulky chlorinated solvent was suggested to act as a template for the formation of the larger pillararene.

Higher Pillararenes

The higher pillararene homologues, pillararene, have been synthesized through the ring expansion of pillararene.

Biomedical applications

A molecular model of carboxylated-pillararene with the anti-Alzheimer drug memantine, showing the total encapsulation of the drug within the macrocycle's cavity. The host–guest complex is stabilized by hydrophobic effects within the cavity, hydrogen bonding, and electrostatic interactions.

While native pillararenes display no solubility in water, and are therefore unsuitable for biomedical applications, a range of water-soluble pillararenes have been reported which have application in drug delivery. In particular, water-soluble carboxylated-pillararenes (where n = 6 or 7) have already shown potential in both drug delivery and bio-diagnostics because they are highly soluble, form host–guest complexes with a range of drug and medicine-based compounds, and appear to be relatively non-toxic. The cavity of carboxylated-pillararene is too small to include most drug molecules and therefore is not useful in drug delivery. To form a host–guest complex with the pillararenes, the drug must have a cationic charge; its ability to hydrogen-bond with the pillararenes is less important. Two planar dye molecules, like proflavine, can be simultaneously encapsulated within the cavity of a single caboxylated-pillararene. Because encapsulation within the cavity of carboxylated-pillararene quenches the fluorescence of proflavine, this gives rise to "on" and "off' states to the dye which may have application in bio-diagnostics.

Other potential applications

Pillararenes have been shown to have potential applications in molecular machinery, sensing, nanoparticle synthesis, artificial transmembrane channels, as components in complex, supramolecular controlled drug delivery systems, construction of porous materials for gas/guest absorption, organic light-emitting materials, and ionic liquids. Binding with dibromoalkanes.

Researchers at Jilin University have reported that a percarboxylated derivative of pillararene inhibits the assembly of the human papillomavirus.

Pillararene shows promise in overcoming the development of antimicrobial resistance and biofilm formation as well as reducing the toxicity of bacterial endotoxins (lipopolysaccharides).

References

  1. Ogoshi, T.; Kanai, S.; Fujinami, S.; Yamagisi, T.; Nakamoto, Y. (2008). "Para-bridged symmetrical pillar 5 arenes: Their Lewis acid catalyzed synthesis and host–guest property". J. Am. Chem. Soc. 130 (15): 5022–5023. doi:10.1021/ja711260m. PMID 18357989.
  2. Cao, D.; Kou, Y.; Liang, J.; Chen, Z.; Wang, L.; Meier, H.; A Facile and Efficient Preparation of Pillararenes and a Pillarquinone. Angew. Chem. Int. Ed. 2009, 48, 9721-9723.
  3. Tan, L.-L.; Zhang, Y.; Li, B.; Wang, K.; Zhang, S. X.-A.; Tao, Y.; Yang, Y.-W. Selective Recognition of "Solvent" Molecules in Solution and the Solid State by 1,4-Dimethoxypillararene Driven by Attractive Forces. New J. Chem. 2014, 38, 845-851.
  4. Rathore, R.; Kochi, J. K. Radical-Cation Catalysis in the Synthesis of Diphenylmethanes via the Dealkylative Coupling of Benzylic Ethers. J. Org. Chem. 1995, 60, 7479–7490.
  5. Ivanov, M. V.; Wang, D.; Navale, T. S.; Lindeman, S. V.; Rathore, R. From Intramolecular (Circular) in an Isolated Molecule to Intermolecular Hole Delocalization in a Two‐Dimensional Solid‐State Assembly: The Case of Pillarene. Angew. Chem. Int. Ed. 2018, 57, 2144-2149.
  6. Strutt, N. L.; Forgan, R. S.; Spruell, J. M.; Botros, Y. Y.; Stoddart, J. F. Monofunctionalized Pillararene as a Host for Alkanediamines. J. Am. Chem. Soc. 2011, 133, 5668-5671.
  7. Ogoshi, T.; Masaki, K.; Shiga, R.; Kitajima, K.; Yamagishi, T.-a. Org. Lett. 2011, 13, 1264
  8. Strutt, N. L., Fairen-Jimenez, D.; Iehl, J.; Lalonde, M. B.; Snurr, R. Q.; Farha, O. K.; Hupp, J. T.; Stoddart, J. F. J. Am. Chem. Soc. 2012, 134, 17436.
  9. Strutt, N. L., Schneebeli, S. T.; Stoddart, J. F. Stereochemical Inversion in Difunctionalised Pillararenes. Supramol. Chem., 2013, 25, 596–608.
  10. Ke, C.; Strutt, N. L.; Li, H.; Hou, X.; Hartlieb, K.; McGonigal, P. R.; Ma, Z.; Iehl, J.; Stern, C. L.; Cheng, C.; Zhu, Z.; Vermeulen, N. A.; Meade, T. J.; Botros, Y. Y.; Stoddart, J. F. Pillararene as a Co-Factor in Templating Rotaxane Formation. J. Am. Chem. Soc. 2013, 135, 17019-17030.
  11. Xue, M.; Yang, Y.; Chi, X.; Zhang, Z.; Huang, F., Pillararenes, A New Class of Macrocycles for Supramolecular Chemistry. Acc. Chem. Res. 2012, 45 (8), 1294–1308.
  12. Liu, L.; Cao, D.; Jin, Y.; Tao, H.; Kou, Y.; Meier, H., Efficient Synthesis of CopillarArenes and Their Host–Guest Properties with Dibromoalkanes. Org. Biomol. Chem. 2011, 9, 7007-7010.
  13. Liu, L.; Cao, D.; Jin, Y.; Tao, H.; Kou, Y.; Meier, H., Efficient Synthesis of CopillarArenes and Their Host–Guest Properties with Dibromoalkanes. Org. Biomol. Chem. 2011, 9, 7007-7010.
  14. Zhang, Z.; Xia, B.; Han, C.; Yu, Y.; Huang, F. Syntheses of Copillararenes by Co-oligomerization of Different Monomers, Organic Letters, 2010, 12, 3285-3287.
  15. Holler, M.; Allenbach, N.; Sonet, J.; Nierengarten, J.-F. The high yielding synthesis of pillararenes under Friedel-Crafts conditions explained by dynamic covalent bond formation. Chem. Commun. 2012, 48, 2576.
  16. Wang, K.; Tan, L.-L.; Chen, D.-X.; Song, N.; Xi, G.; Zhang, S. X.-A.; Li, C.; Yang, Y.-W. One-Pot Synthesis of Pillararenes Catalyzed by a Minimum Amount of TfOH and a Solution-Phase Mechanistic Study. Org. Biomol. Chem. 2012, 10, 9405-9409.
  17. Synthesis and host–guest properties of pillararenes. Sci. China Chem. 2012, 55, 223-228.
  18. The template effect of solvents on high yield synthesis, co-cyclization of pillararenes and interconversion between pillar- and pillararenes. Chem. Commun. 2014, 50, 5774-5777.
  19. Tomoki Ogoshi, Naosuke Ueshima, Fumiyasu Sakakibara, Tada-aki Yamagishi, and Takeharu Haino. Conversion from Pillararene to Pillararenes by Ring Expansion and Encapsulation of C60 by Pillararenes with Nanosize Cavities. Org. Lett. 2014, 16, 2896-2899. doi:10.1021/ol501039u.
  20. Gu, Alice; Wheate, Nial (2021). "Macrocycles as drug-enhancing excipients in pharmaceutical formulations". Journal of Inclusion Phenomena and Macrocyclic Chemistry. 100 (1–2): 55–69. doi:10.1007/s10847-021-01055-9. S2CID 233139034.
  21. Wheate, Nial; Dickson, Kristie-Ann; Kim, Ryung Rae; Nematollahi, Alireza; Macquart, Rene; Kayser, Veysel; Yu, Guocan; Church, W. Bret; Marsh, Deborah (2016). "Host–Guest Complexes of Carboxylated Pillararenes With Drugs". Journal of Pharmaceutical Sciences. 105 (12): 3615–3625. doi:10.1016/j.xphs.2016.09.008. PMID 27776769.
  22. Hou, X.; Ke, C.; Cheng, C.; Song, N.; Blackburn, A. K.; Sarjeant, A. A.; Botros, Y. Y.; Yang, Y.-W.; Stoddart, J. F. Efficient Syntheses of Pillararene-Based Heterorotaxanes Using a Cooperative Capture Strategy. Chem. Commun. 2014, 50, 6196-6199.
  23. Taylor, Andrew J.; Wilmore, Jamie T.; Beer, Paul D. (2024). "Halogen bonding BODIPY-appended pillar[5]arene for the optical sensing of dicarboxylates and a chemical warfare agent simulant". Chemical Communications. doi:10.1039/D4CC03748K.
  24. Li, H.; Chen, D.-X.; Sun, Y.-L.; Zheng, Y. B.; Tan, L.-L.; Weiss, P. S.; Yang, Y.-W. Viologen-Mediated Assembly of and Sensing with Carboxylatopillararene-Modified Au Nanoparticles. J. Am. Chem. Soc. 2013, 135, 1570-1576.
  25. Yao, Y.; Xue, M.; Chi, X.; Ma, Y.; He, J.; Abliz, Z.; Huang, F. A New Water-Soluble Pillararene: Synthesis and Application in the Preparation of Gold Nanoparticles. Chem. Commun. 2012, 48, 6505−6507.
  26. Si, W.; Chen, L.; Hu, X.-B.; Tang, G.; Chen, Z.; Hou, J.-L.; Li, Z.-T. Selective Artificial Transmembrane Channels for Protons by Formation of Water Wires. Angew. Chem. Int. Ed. 2011, 50, 12564–12568.
  27. Sun, Y.-L.; Yang, Y.-W.; Chen, D.-X.; Wang, G.; Zhou, Y.; Wang, C.-Y.; Stoddart, J. F. Mechanized Silica Nanoparticles Based on Pillararenes for On-Command Cargo Release. Small 2013, 9, 3224-3229.
  28. Duan, Q.; Cao, Y.; Li, Y.; Hu, X.; Xiao, T.; Lin, C.; Pan, Y.; Wang, L. pH-Responsive Supramolecular Vesicles Based on Water-Soluble Pillararene and Ferrocene Derivative for Drug Delivery. J. Am. Chem. Soc. 2013, 135, 10542–10549.
  29. Strutt, N. L.; Fairen-Jimenez, D.; Iehl, J.; LaLonde, M. B.; Snurr, R. Q.; Farha, O. K.; Hupp, J. T.; Stoddart, J. F. Incorporation of an A1/A2-difunctionalized pillararene into a metal–organic framework. J. Am. Chem. Soc. 2012, 134, 17436—17439
  30. Tan, L.-L.; Li, H.; Tao, Y.; Zhang, S. X.-A.; Wang, B.; Yang, Y.-W. Pillarene-Based Supramolecular Organic Frameworks for Highly Selective Carbon Dioxide Storage under Ambient Conditions. Adv. Mater. 2014, 26, 7027–7031.
  31. Song, N.; Chen, D.-X.; Qiu, Y.-C.; Yang, X.-Y.; Xu, B.; Tian, W.; Yang, Y.-W. Stimuli-Responsive Blue Fluorescent Supramolecular Polymers Based on a Pillararene Tetramer. Chem. Commun. 2014, 50, 8231–8234.
  32. Song, N.; Chen, D.-X.; Xia, M.-C.; Qiu, X.-L.; Ma, K.; Xu, B.; Tian, W.; Yang, Y.-W. Supramolecular Assembly-Induced Yellow Emission of 9,10-Distyrylanthracene Bridged Bis(pillararene)s. Chem. Commun. 2014, doi:10.1039/C4CC08205B.
  33. Liu, L.; Cao, D.; Jin, Y.; Tao, H.; Kou, Y.; Meier, H., Efficient Synthesis of CopillarArenes and Their Host–Guest Properties with Dibromoalkanes. Org. Biomol. Chem. 2011, 9, 7007-7010.
  34. Zheng, D.-D.; Fu, D.-Y.; Wu, Y.-Q.;* Sun, Y.-L.; Tan, L.-L.; Zhou, T.; Ma, S.-Q.; Zha, X.; Yang, Y.-W. Efficient Inhibition of Human Papillomavirus 16 L1 Pentamer Formation by a Carboxylatopillarene and a p-Sulfonatocalixarene. Chem. Commun. 2014, 50, 3201-3203.
  35. Jonkergouw, C., Beyeh, N.K., Osmekhina, E. et al. Repurposing host-guest chemistry to sequester virulence and eradicate biofilms in multidrug resistant Pseudomonas aeruginosa and Acinetobacter baumannii. Nat Commun 14, 2141 (2023). https://doi.org/10.1038/s41467-023-37749-6
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