Adsorption of the urea molecule on the B12N12 nanocage

The adsorption of the urea molecule on the external surface of the B12N12 nanocage was investigated using density functional theory (DFT) calculations. Adsorption of urea on the nanocage releases energies of about --23.70 to --29.50 kcal/mol with a significant NBO charge transfer from the urea to the nanocage. It was also found that the urea molecule can be strongly chemisorbed on the surface of the nanocage with Gibbs free energies of -7.91 to -14.81 kcal/mol. The HOMO--LUMO gap of the nanocage does not change significantly upon urea adsorption, while the Fermi level is dramatically changed from -4.27 eV in the pristine nanocage to upper energies upon urea adsorption. The geometric structure, adsorption energy, solvation effect, charge transfer, and frequency analyses of the urea adsorption on the nanocage models showed that the urea molecule could be firmly adsorbed by the nanocage and the nanocage could be a potential efficient adsorbent for the adsorption of urea.

Adsorption of the urea molecule on the B12N12 nanocage

The adsorption of the urea molecule on the external surface of the B12N12 nanocage was investigated using density functional theory (DFT) calculations. Adsorption of urea on the nanocage releases energies of about --23.70 to --29.50 kcal/mol with a significant NBO charge transfer from the urea to the nanocage. It was also found that the urea molecule can be strongly chemisorbed on the surface of the nanocage with Gibbs free energies of -7.91 to -14.81 kcal/mol. The HOMO--LUMO gap of the nanocage does not change significantly upon urea adsorption, while the Fermi level is dramatically changed from -4.27 eV in the pristine nanocage to upper energies upon urea adsorption. The geometric structure, adsorption energy, solvation effect, charge transfer, and frequency analyses of the urea adsorption on the nanocage models showed that the urea molecule could be firmly adsorbed by the nanocage and the nanocage could be a potential efficient adsorbent for the adsorption of urea.

___

  • Beheshtian, J., Peyghan, A. A., Tabar, M. B., Bagheri, Z. Appl. Surf. Sci. 2013, 266, 182-187.
  • Gao, Y., Zhao, N., Wei, W., Sun, Y. Computational and Theoretical Chemistry 2012, 992, 1–8.
  • Lee, C. J., Hsu, S. T. J. Biomed. Mater. Res. 1990, 24, 243–258.
  • Shimizu, T., Fujishige, S. J. Biomed. Mater. Res. 1983, 17, 597–612.
  • Yagi, M., Kato, S., Nishitoba, T. Nephrology 1998, 78, 433–439.
  • Wolfe, E. A., Chang, T. M. S. Int. J. Artif. Organs. 1987, 10, 269–274.
  • Peyghan, A. A., Baei, M. T., Hashemian, S. J. Clust. Sci. 2013, 24, 341–347.
  • Beheshtian, J. Kamfiroozi, M. Bagheri, Z. Ahmadi, A. Comp. Mater. Sci. 2012, 54, 115–118.
  • Baei, M. T. J. Clust. Sci. 2013, 24, 749–756.
  • Baei, M. T . Peyghan, A. A., Bagheri, Z. Bull. Korean Chem. Soc. 2012, 33, 3338–3342.
  • Baei, M. T., Bagheri, Z., Peyghan, A. A. Struct. Chem. 2012, 24, 1039–1044.
  • Seifert, G., Fowler, R. W., Mitchell, D., Porezag, D., Frauenheim, T. Chem. Phys. Lett. 1997, 268, 352–358.
  • Oku, T., Nishiwaki, A., Narita, I. Sci. Technol. Adv. Mater. 2004, 5, 635–645.
  • Kim, C., Kim, B., Lee, S. M., Jo, C., Lee, Y. H. Phys. Rev. B. 2002, 65, 165418 (1)– 165418 (6).
  • Zhao, Y., Truhlar, D. G. Acc. Chem. Res. 2008, 41, 157–167.
  • Schmidt, M.; Baldridge, K. K.; Boatz, J. A.; Elbert, S. T.; Gordon, M. S.; Jensen, J. H.; Koseki, S.; Matsunaga, N.; Nguyen, K. A.; Su, S.; et al. J. Comput. Chem. 1993, 14, 1347–1363.
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Synthesis and characterization of a novel 3-amino-1,2,4-triazole lead(II) coordination polymer

Şebnem Esen SÖZERLİ, Arzu ÖZEN, İbrahim KANİ, Deniz DEMİR

Thermal conversion of glycerol to value-added chemicals: pyridine derivatives by one-pot microwave-assisted synthesis

Duygu BAYRAMOĞLU, Gökay GÜREL, Ali SINAĞ, Mustafa GÜLLÜ

Oxidation of hydrocarbons with tetra-n-butylammonium peroxy monosulfate catalyzed by β -tetrabromo-meso-tetrakis(4-methoxyphenyl)- and β -tetrabromo-meso-tetraphenylporphyrinatomanganese(III)

Saeed RAYATI, Saeed ZAKAVI, Hossein VALINEJAD

Synthesis, spectral characterisation, electrochemical, and fluorescence studies of biologically active novel Schiff base complexes derived from E-4-(2-hydroxy-3-methoxybenzlideneamino)-N-(pyrimidin-2-yl)benzenesulfonamide

Valarmathy GOVINDARAJ, Subbalakshmi RAMANATHAN

Catalytic conversion of carbon dioxide into cyclic carbonates by Cu(II) and Ni(II) acetylacetonates anchored onto Siral 80

Senem COŞKUN, Zeynep TAŞÇI, Mahmut ULUSOY, Mürüvvet YURDAKOÇ

Antioxidant, anticholinesterase, and antimicrobial activities and fatty acid constituents of Achillea cappadocica Hausskn. et Bornm.

Abdulselam ERTAŞ, Mehmet BOĞA, Nesrin HAŞİMİ, Yeter YEŞİL, Ahmet Ceyhan GOREN, Gülaçtı TOPÇU, Ufuk KOLAK

Development of 2-acetylpyridine-4-phenyl-3-thiosemicarbazone functionalized polymeric resin for the preconcentration of metal ions prior to their ultratrace determinations by MIS-FAAS

Ali Nawaz SIYAL, Saima Qayoom MEMON, Aydan ELÇİ

Convenient synthesis of new polysubstituted isoindole-1,3-dione analogues

Ayşe TAN, Mustafa Zahrittin KAZANCIOĞLU, Derya AKTAŞ, Özlem GÜNDOĞDU, Ertan ŞAHİN, Nurhan HORASAN KİSHALI, Yunus KARA

Adsorption of the urea molecule on the B12N12 nanocage

Mohammad Taghi BAEI

Partial purification and biochemical characterization of an extremely thermo- and pH-stable esterase with great substrate affinity

Esra ÖZBEK, Yakup KOLCUOĞLU, Leyla KONAK, Ahmet ÇOLAK, Fulya ÖZ