Vitor C. Weiss , Giliandro Farias , Suélen M. Amorim , André L. Amorim , Daniele C. Durigon , Fernando R. Xavier , Regina de F.P.M. Moreira , Adailton J. Bortoluzzi , Rosely A. Peralta
{"title":"水溶性Re(I)光corms释放CO的理论和实验机理研究","authors":"Vitor C. Weiss , Giliandro Farias , Suélen M. Amorim , André L. Amorim , Daniele C. Durigon , Fernando R. Xavier , Regina de F.P.M. Moreira , Adailton J. Bortoluzzi , Rosely A. Peralta","doi":"10.1016/j.ica.2025.122788","DOIUrl":null,"url":null,"abstract":"<div><div>The use of photoCORMs to release carbon monoxide in a specific biological target has been widely studied because their therapeutic properties. This work presents the synthesis and photochemical and mechanistic insight of the CO photorelease of three water-soluble Re(I) photoCORMs: [Re(aaz)(CO)<sub>3</sub>]Cl (<strong>1</strong>), [Re(Me<sub>2</sub>aaz)(CO)<sub>3</sub>]Cl (<strong>2</strong>), and [Re(tacn)(CO)<sub>3</sub>]Cl (<strong>3</strong>) (aaz = 6-amino-6-methylperhydro-1,4-diazepine; Me<sub>2</sub>aaz = 6-amino-1,4,6-trimethyl-1,4-diazacycloheptane; and tacn = 1,4,7-triazacyclononane). All compounds presented photo-triggered carbon monoxide release when exposed to UV light (λ<sub>254</sub> = 254 ± 10 nm), affording bis and monocarbonyl intermediates identified via spectroscopic, electrochemical, and mass techniques. The quantum yields and rates of CO release were determined where its release mechanism probably involves a three-step mechanistic pathway. Despite recent studies, the mechanism of CO release associated with Re(I) photoCORMs and spin-orbit coupling has not been explored in-depth, and it could be a critical factor in developing new and more efficient photoCORMs.</div></div>","PeriodicalId":13599,"journal":{"name":"Inorganica Chimica Acta","volume":"587 ","pages":"Article 122788"},"PeriodicalIF":2.7000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Theoretical and experimental mechanistic insights of CO release by water soluble Re(I) photoCORMs\",\"authors\":\"Vitor C. Weiss , Giliandro Farias , Suélen M. Amorim , André L. Amorim , Daniele C. Durigon , Fernando R. Xavier , Regina de F.P.M. Moreira , Adailton J. Bortoluzzi , Rosely A. Peralta\",\"doi\":\"10.1016/j.ica.2025.122788\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The use of photoCORMs to release carbon monoxide in a specific biological target has been widely studied because their therapeutic properties. This work presents the synthesis and photochemical and mechanistic insight of the CO photorelease of three water-soluble Re(I) photoCORMs: [Re(aaz)(CO)<sub>3</sub>]Cl (<strong>1</strong>), [Re(Me<sub>2</sub>aaz)(CO)<sub>3</sub>]Cl (<strong>2</strong>), and [Re(tacn)(CO)<sub>3</sub>]Cl (<strong>3</strong>) (aaz = 6-amino-6-methylperhydro-1,4-diazepine; Me<sub>2</sub>aaz = 6-amino-1,4,6-trimethyl-1,4-diazacycloheptane; and tacn = 1,4,7-triazacyclononane). All compounds presented photo-triggered carbon monoxide release when exposed to UV light (λ<sub>254</sub> = 254 ± 10 nm), affording bis and monocarbonyl intermediates identified via spectroscopic, electrochemical, and mass techniques. The quantum yields and rates of CO release were determined where its release mechanism probably involves a three-step mechanistic pathway. Despite recent studies, the mechanism of CO release associated with Re(I) photoCORMs and spin-orbit coupling has not been explored in-depth, and it could be a critical factor in developing new and more efficient photoCORMs.</div></div>\",\"PeriodicalId\":13599,\"journal\":{\"name\":\"Inorganica Chimica Acta\",\"volume\":\"587 \",\"pages\":\"Article 122788\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganica Chimica Acta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0020169325002543\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganica Chimica Acta","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0020169325002543","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Theoretical and experimental mechanistic insights of CO release by water soluble Re(I) photoCORMs
The use of photoCORMs to release carbon monoxide in a specific biological target has been widely studied because their therapeutic properties. This work presents the synthesis and photochemical and mechanistic insight of the CO photorelease of three water-soluble Re(I) photoCORMs: [Re(aaz)(CO)3]Cl (1), [Re(Me2aaz)(CO)3]Cl (2), and [Re(tacn)(CO)3]Cl (3) (aaz = 6-amino-6-methylperhydro-1,4-diazepine; Me2aaz = 6-amino-1,4,6-trimethyl-1,4-diazacycloheptane; and tacn = 1,4,7-triazacyclononane). All compounds presented photo-triggered carbon monoxide release when exposed to UV light (λ254 = 254 ± 10 nm), affording bis and monocarbonyl intermediates identified via spectroscopic, electrochemical, and mass techniques. The quantum yields and rates of CO release were determined where its release mechanism probably involves a three-step mechanistic pathway. Despite recent studies, the mechanism of CO release associated with Re(I) photoCORMs and spin-orbit coupling has not been explored in-depth, and it could be a critical factor in developing new and more efficient photoCORMs.
期刊介绍:
Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews.
Topics covered include:
• chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies;
• synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs);
• reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models;
• applications of inorganic compounds, metallodrugs and molecule-based materials.
Papers composed primarily of structural reports will typically not be considered for publication.