Carbonyl hypoiodites from pivalic and trimesic acid and their silver(I) intermediates
| dc.contributor.author | Ward, Jas S. | |
| dc.contributor.author | Martõnova, Jevgenija | |
| dc.contributor.author | Wilson, Laura M. E. | |
| dc.contributor.author | Kramer, Eric | |
| dc.contributor.author | Aav, Riina | |
| dc.contributor.author | Rissanen, Kari | |
| dc.date.accessioned | 2022-09-14T08:38:18Z | |
| dc.date.available | 2022-09-14T08:38:18Z | |
| dc.date.issued | 2022 | |
| dc.identifier.citation | Ward, J. S., Martõnova, J., Wilson, L. M. E., Kramer, E., Aav, R., & Rissanen, K. (2022). Carbonyl hypoiodites from pivalic and trimesic acid and their silver(I) intermediates. <i>Dalton Transactions</i>, <i>51</i>(38), 14646-14653. <a href="https://doi.org/10.1039/d2dt01988d" target="_blank">https://doi.org/10.1039/d2dt01988d</a> | |
| dc.identifier.other | CONVID_156485036 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/83247 | |
| dc.description.abstract | The first tris(O–I–N) carbonyl hypoiodites have been synthesised based on trimesic acid and pyridine or 4-methylpyridine, with their structures definitively confirmed by single crystal X-ray diffraction (SCXRD). The more soluble carbonyl hypoiodites based on pivalic acid have also been studied via NMR, SCXRD, and computational analyses, enabling the study of the direct silver(I) precursor and intermediates of the resulting carbonyl hypoiodites generated using a range of substituted pyridines. | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | eng | |
| dc.publisher | Royal Society of Chemistry (RSC) | |
| dc.relation.ispartofseries | Dalton Transactions | |
| dc.rights | CC BY 4.0 | |
| dc.title | Carbonyl hypoiodites from pivalic and trimesic acid and their silver(I) intermediates | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-202209144593 | |
| 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 | 14646-14653 | |
| dc.relation.issn | 1477-9226 | |
| dc.relation.numberinseries | 38 | |
| dc.relation.volume | 51 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © The Royal Society of Chemistry 2022 | |
| dc.rights.accesslevel | openAccess | fi |
| dc.relation.grantnumber | 317259 | |
| dc.subject.yso | jodi | |
| dc.subject.yso | kemialliset sidokset | |
| dc.subject.yso | kompleksiyhdisteet | |
| dc.subject.yso | halogeenit | |
| dc.subject.yso | hopea | |
| dc.subject.yso | karbonyylit | |
| dc.format.content | fulltext | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p18902 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p10130 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p30190 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p4164 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p7409 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p14898 | |
| dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
| dc.relation.doi | 10.1039/d2dt01988d | |
| dc.relation.funder | Research Council of Finland | en |
| dc.relation.funder | Suomen Akatemia | fi |
| jyx.fundingprogram | Academy Project, AoF | en |
| jyx.fundingprogram | Akatemiahanke, SA | fi |
| jyx.fundinginformation | The authors would like to thank the University of Jyväskylä mass spectrometry service for their time and expertise, and gratefully acknowledge the Magnus Ehrnrooth Foundation (J. S. W.), the ERDF DORA travel grant (J. M.), the Estonian Research Council (R.A. grant no. PRG399), the Academy of Finland (K.R. grant no. 317259), and the University of Jyväskylä, Finland for financial support. | |
| dc.type.okm | A1 |
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