» Articles » PMID: 32983269

Synthetic Approaches to Bowl-shaped π-conjugated Sumanene and Its Congeners

Overview
Specialty Chemistry
Date 2020 Sep 28
PMID 32983269
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Since the first synthetic report in 2003 by Sakurai et al., sumanene (derived from the Indian 'Hindi as well as Sanskrit word' "Suman", which means "Sunflower"), a beautifully simple yet much effective bowl-shaped -symmetric polycyclic aromatic hydrocarbon having three benzylic positions clipped between three phenyl rings in the triphenylene framework has attracted a tremendous attention of researchers worldwide. Therefore, since its first successful synthesis, a variety of functionalized sumanenes as well as heterosumanenes have been developed because of their unique physiochemical properties. For example, bowl-to-bowl inversion, bowl depth, facial selectivity, crystal packing, metal complexes, intermolecular charge transfer systems, cation-π complexation, electron conductivity, optical properties and so on. Keeping the importance of this beautiful scaffold in mind, we compiled all the synthetic routes available for the construction of sumanene and its heteroatom derivatives including Mehta's first unsuccessful effort up to the latest achievements. Our major goal to write this review article was to provide a quick summary of where the field has been, where it stands at present, and where it might be going in near future. Although several reviews have been published on sumanene chemistry dealing with different aspects but this is the first report that comprehensively describes the 'all-in-one' chemistry of the sumanene architecture since its invention to till date. We feel that this attractive review article will definitely help the scientific community working not only in the area of organic synthesis but also in materials science and technology.

Citing Articles

-Symmetric Indole-Based Truxenes: Design, Synthesis, and Photophysical Studies.

Alvi S, Sil A, Maity S, Singh V, Guchhait B, Ali R ACS Omega. 2024; 9(8):9098-9108.

PMID: 38434898 PMC: 10905574. DOI: 10.1021/acsomega.3c07770.


Syntheses, Structures and Reactivity of Metal Complexes of Trindane, Trindene, Truxene, Decacyclene and Related Ring Systems: Manifestations of Three-Fold Symmetry.

Lock P, Reginato N, Bruno-Colmenarez J, McGlinchey M Molecules. 2023; 28(23).

PMID: 38067526 PMC: 10707772. DOI: 10.3390/molecules28237796.


Application of Monoferrocenylsumanenes Derived from Sonogashira Cross-Coupling or Reactions in Highly Sensitive and Selective Cesium Cation Electrochemical Sensors.

Kasprzak A, Gajda-Walczak A, Kowalczyk A, Wagner B, Nowicka A, Nishimoto M J Org Chem. 2023; 88(7):4199-4208.

PMID: 36916291 PMC: 10088032. DOI: 10.1021/acs.joc.2c02767.


Dithieno[3,2-:2',3'-]thiophene (DTT): an emerging heterocyclic building block for future organic electronic materials & functional supramolecular chemistry.

Ali R, Siddiqui R RSC Adv. 2022; 12(55):36073-36102.

PMID: 36545080 PMC: 9756821. DOI: 10.1039/d2ra05768a.


An Efficient and Versatile Deep Eutectic Solvent-Mediated Green Method for the Synthesis of Functionalized Coumarins.

Rather I, Ali R ACS Omega. 2022; 7(12):10649-10659.

PMID: 35382332 PMC: 8973037. DOI: 10.1021/acsomega.2c00293.


References
1.
Ngamsomprasert N, Dang J, Higashibayashi S, Yakiyama Y, Sakurai H . Sumanene derivatives functionalized at the internal carbon. Chem Commun (Camb). 2016; 53(4):697-700. DOI: 10.1039/c6cc08970d. View

2.
Topolinski B, Schmidt B, Higashibayashi S, Sakurai H, Lentz D . Sumanenylferrocenes and their solid state self-assembly. Dalton Trans. 2013; 42(38):13809-12. DOI: 10.1039/c3dt51569a. View

3.
Kasprzak A, Kowalczyk A, Jagielska A, Wagner B, Nowicka A, Sakurai H . Tris(ferrocenylmethidene)sumanene: synthesis, photophysical properties and applications for efficient caesium cation recognition in water. Dalton Trans. 2020; 49(29):9965-9971. DOI: 10.1039/d0dt01506g. View

4.
Li X, Zhu Y, Shao J, Wang B, Zhang S, Shao Y . Non-pyrolytic, large-scale synthesis of trichalcogenasumanene: a two-step approach. Angew Chem Int Ed Engl. 2014; 53(2):535-8. DOI: 10.1002/anie.201308781. View

5.
Armakovic S, Armakovic S, Setrajcic J, Jacimovski S, Holodkov V . Sumanene and its adsorption properties towards CO, CO₂ and NH₃ molecules. J Mol Model. 2014; 20(4):2170. DOI: 10.1007/s00894-014-2170-3. View