dc.contributor.author | Twum, Kwaku | |
dc.contributor.author | Iraj Sadraei, Seyed | |
dc.contributor.author | Feder, Jordan | |
dc.contributor.author | Taimoory, S. Maryamdokht | |
dc.contributor.author | Rissanen, Kari | |
dc.contributor.author | Trant, John F. | |
dc.contributor.author | Beyeh, Ngong Kodiah | |
dc.date.accessioned | 2022-02-28T09:38:57Z | |
dc.date.available | 2022-02-28T09:38:57Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Twum, K., Iraj Sadraei, S., Feder, J., Taimoory, S. M., Rissanen, K., Trant, J. F., & Beyeh, N. K. (2022). Sharing the salt bowl : counterion identity drives N-alkyl resorcinarene affinity for pyrophosphate in water. <i>Organic Chemistry Frontiers</i>, <i>9</i>(5), 1267-1275. <a href="https://doi.org/10.1039/D1QO01877A" target="_blank">https://doi.org/10.1039/D1QO01877A</a> | |
dc.identifier.other | CONVID_104377637 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/79986 | |
dc.description.abstract | N-Alkyl ammonium resorcinarene chloride receptors, NARX4, have been shown to act as high-sensitivity detectors of pyrophosphate (PPi), a biomarker of disease, in aqueous media through the chloride-to-PPi exchange [NAR(Cl)4 to NARPPi]. The nature of the anion of the macrocyclic NARX4 (X = Cl−, Br−, triflate OTf−) receptor greatly influences the PPi-affinity in aqueous media. The binding affinity for [NAR (Cl)4] is 3.61 × 105 M−1, while the NAR (Br)4 and NAR (OTf)4 show stronger binding of 5.30 × 105 M−1, and 6.10 × 105 M−1, respectively. The effects of upper rim ammonium cation, –N+H2R substituents (R = 3-hydroxypropyl, cyclohexyl, benzyl, or napththalen-1-ylmethyl), of the macrocyclic resorcinarene hosts have also been evaluated. The highest affinity was obtained using 3-hydroxypropyl groups due to the additional hydrogen bonds and the naphthyl upper-rim group that provides a larger hydrophobic surface area and favorable stacking interaction (i.e., π–π and CH–π). We note that two PPi molecules can bind to the more selective receptors through an additional interaction with the lower rim hydroxyls, making the resorcinarene a divalent binder. Comparing PPi with other phosphate anions (PO43−, AMP, ADP, and ATP) shows that the receptors are more selective for PPi due to the size and charge complementarity. Experimental (1H, 31P NMR, and isothermal titration calorimetry), and computational analyses support the reported trends for PPi selectivity even in highly competing aqueous media. | en |
dc.format.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Royal Society of Chemistry (RSC) | |
dc.relation.ispartofseries | Organic Chemistry Frontiers | |
dc.rights | CC BY 4.0 | |
dc.title | Sharing the salt bowl : counterion identity drives N-alkyl resorcinarene affinity for pyrophosphate in water | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-202202281709 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Orgaaninen kemia | fi |
dc.contributor.oppiaine | Organic Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 1267-1275 | |
dc.relation.issn | 2052-4110 | |
dc.relation.numberinseries | 5 | |
dc.relation.volume | 9 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2022 the Partner Organisations | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | biomarkkerit | |
dc.subject.yso | supramolekulaarinen kemia | |
dc.subject.yso | fosfaatit | |
dc.subject.yso | liuokset | |
dc.subject.yso | kemialliset sidokset | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p12288 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p37759 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8696 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p4335 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p10130 | |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.1039/D1QO01877A | |
jyx.fundinginformation | The authors gratefully acknowledge financial support from the Provost Graduate Research Scholarship (KT, JF), Oakland University, MI, USA, and the University of Windsor, ON, Canada. This work was made possible by the facilities of the Shared Hierarchical Academic Research Computing Network (SHARCNET: http://www.sharcnet.ca) and Compute/Calcul Canada. This work was funded in part by the Natural Sciences and Engineering Research Council of Canada (Grant # 2018-06338 to JFT), the Windsor Cancer Centre Foundation Seeds4Hope Seed Grant Funding Program (Grant # 2017-03 to JFT), and an Ontario Early Researcher Award (Grant # ER18-14-114 to JFT). | |
dc.type.okm | A1 | |