TY - JOUR
T1 - Investigating the Interaction of Anthracene and Phenanthrene with Cucurbit[n]urils (n=6-8)
T2 - Experimental and Molecular Dynamics Studies
AU - Alfadil, Amira A.
AU - Elbashir, Abdalla A.
AU - Omar, Mei Musa Ali
AU - Suliman, Fakhr Eldin O.
N1 - Funding Information:
Ms. Amira Anwar thanks Organization for Women in Science for the Developing World (OWSD) for a Ph.D. scholarship at SQU. The technical support by Central Analytical and Applied Research Unit (CAARU) at SQU is acknowledged. The authors would like to thank: the Arab-German Young Academy of Sciences and Humanities (AGYA) for research funding and the Ministry of Higher Education & Scientific Research, Commission of Scientific research and Innovation-Sudan.
Funding Information:
. Ms. Amira Anwar thanks Organization for Women in Science for the Developing World (OWSD) for a Ph.D. scholarship at SQU. The technical support by Central Analytical and Applied Research Unit (CAARU) at SQU is acknowledged. The authors would like to thank: the Arab‐German Young Academy of Sciences and Humanities (AGYA) for research funding and the Ministry of Higher Education & Scientific Research, Commission of Scientific research and Innovation‐Sudan
Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/10/7
Y1 - 2022/10/7
N2 - The supramolecular interaction of anthracene (ANT) and phenanthrene (PHN) with cucurbit[n]uril, CB[n] (n=6-8) has been investigated in aqueous media for the first time. The inclusion complexes were investigated and characterized by fluorescence spectroscopy, matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry, and 1HNMR. The stability of these complexes and the mode of inclusion in aqueous media at atomistic levels were monitored by molecular dynamic (MD) simulations. The results obtained from the experimental and MD studies have demonstrated the formation of stable 1 : 1 complexes between the two guests with all hosts in aqueous media. From the fluorescence study, the binding constants of PHN with CB[6], CB[7], and CB[8] were found to be 398±63, 544±128, and 655±162 M−1, respectively. Whereas, ANT- CB[n] formation constants are 213±37 M−1 270±35 M−1, and 356±94 M−1 for CB[6], CB[7], and CB[8], respectively. The results obtained show that the size of the cavity of the macrocycle and the polarity of the rim play an important role in the stability of the formed complex. Surprisingly, CB[6] forms an inclusion complex with ANT while it interacts by its side with PHN through dipole-dipole interaction. The larger cavity sizes of CB[7], CB[8], were found to encapsulate the two guests forming highly stable inclusion complexes.
AB - The supramolecular interaction of anthracene (ANT) and phenanthrene (PHN) with cucurbit[n]uril, CB[n] (n=6-8) has been investigated in aqueous media for the first time. The inclusion complexes were investigated and characterized by fluorescence spectroscopy, matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry, and 1HNMR. The stability of these complexes and the mode of inclusion in aqueous media at atomistic levels were monitored by molecular dynamic (MD) simulations. The results obtained from the experimental and MD studies have demonstrated the formation of stable 1 : 1 complexes between the two guests with all hosts in aqueous media. From the fluorescence study, the binding constants of PHN with CB[6], CB[7], and CB[8] were found to be 398±63, 544±128, and 655±162 M−1, respectively. Whereas, ANT- CB[n] formation constants are 213±37 M−1 270±35 M−1, and 356±94 M−1 for CB[6], CB[7], and CB[8], respectively. The results obtained show that the size of the cavity of the macrocycle and the polarity of the rim play an important role in the stability of the formed complex. Surprisingly, CB[6] forms an inclusion complex with ANT while it interacts by its side with PHN through dipole-dipole interaction. The larger cavity sizes of CB[7], CB[8], were found to encapsulate the two guests forming highly stable inclusion complexes.
KW - Anthracene
KW - Cucurbituril
KW - Inclusion Compounds
KW - Molecular Dynamics
KW - Phenanthrene
KW - Poly Aromatic Hydrocarbons (PAH)
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U2 - 10.1002/slct.202203043
DO - 10.1002/slct.202203043
M3 - Article
AN - SCOPUS:85139529135
SN - 2365-6549
VL - 7
JO - ChemistrySelect
JF - ChemistrySelect
IS - 37
M1 - e202203043
ER -