Yayın:
Phenolic Compounds in Black Grape by the Electronic and Thermochemical Studies

dc.date.accessioned2026-01-05T22:34:29Z
dc.date.issued2022-03-29
dc.description.abstractThis investigation analyzes the effects of light and genotype on the biosynthesis of anthocyanins. The applied plant material, including dye grape varieties, accumulates anthocyanins in the skin and the pulp and hybrid populations. Anthocyanins are secondary plant metabolites with the response of most of the red to purple pigmentation existing in fruits, vegetables, and flowers. During grape berry development, these compounds are accumulated from maturation until ripening and are responsible for pigmentation found in red skin berries. Several cations linked to anthocyanins in H2O molecules have been investigated for studying the color difference of various compounds in the low limitations of pH value. In this accomplishment, cations attached to Mal, Peo, Del, Pet, and Cya in water has been simulated, converting flavylium cations to the blue quinonoidal bases at a lower amount of pH using the IR approach by installing the beer-lambert law for getting the physicochemical properties of absorbance, intensity and of the structures. The changes of enthalpy between complexes of anthocyanins-cations have been discussed due to carbonyl groups and double bonds by the (B)-ring chelated of cyanidin, delphinidin, and petunidin anthocyanins in different media of gas and water which illustrates the stability and color of anthocyanin-cations chelated to Mal, Peo, Del, Pet, and Cya colorful pigments in a weakly acidic medium.
dc.description.urihttps://doi.org/10.33263/briac132.162
dc.identifier.doi10.33263/briac132.162
dc.identifier.eissn2069-5837
dc.identifier.openairedoi_________::7eab46c26a2b77cf994984ed167e2589
dc.identifier.scopus2-s2.0-85205872619
dc.identifier.startpage162
dc.identifier.urihttps://hdl.handle.net/20.500.12597/43219
dc.identifier.volume13
dc.identifier.wos000828464500050
dc.language.isoeng
dc.publisherAMG Transcend Association
dc.relation.ispartofBiointerface Research in Applied Chemistry
dc.rightsOPEN
dc.titlePhenolic Compounds in Black Grape by the Electronic and Thermochemical Studies
dc.typeArticle
dspace.entity.typePublication
local.api.response{"authors":null,"openAccessColor":"gold","publiclyFunded":false,"type":"publication","language":{"code":"eng","label":"English"},"countries":null,"subjects":null,"mainTitle":"Phenolic Compounds in Black Grape by the Electronic and Thermochemical Studies","subTitle":null,"descriptions":["<jats:p>This investigation analyzes the effects of light and genotype on the biosynthesis of anthocyanins. The applied plant material, including dye grape varieties, accumulates anthocyanins in the skin and the pulp and hybrid populations. Anthocyanins are secondary plant metabolites with the response of most of the red to purple pigmentation existing in fruits, vegetables, and flowers. During grape berry development, these compounds are accumulated from maturation until ripening and are responsible for pigmentation found in red skin berries. Several cations linked to anthocyanins in H2O molecules have been investigated for studying the color difference of various compounds in the low limitations of pH value. In this accomplishment, cations attached to Mal, Peo, Del, Pet, and Cya in water has been simulated, converting flavylium cations to the blue quinonoidal bases at a lower amount of pH using the IR approach by installing the beer-lambert law for getting the physicochemical properties of absorbance, intensity and of the structures. The changes of enthalpy between complexes of anthocyanins-cations have been discussed due to carbonyl groups and double bonds by the (B)-ring chelated of cyanidin, delphinidin, and petunidin anthocyanins in different media of gas and water which illustrates the stability and color of anthocyanin-cations chelated to Mal, Peo, Del, Pet, and Cya colorful pigments in a weakly acidic medium.</jats:p>"],"publicationDate":"2022-03-29","publisher":"AMG Transcend Association","embargoEndDate":null,"sources":["Crossref"],"formats":null,"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_abf2","label":"OPEN","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":{"name":"Biointerface Research in Applied Chemistry","issnPrinted":null,"issnOnline":"2069-5837","issnLinking":null,"ep":null,"iss":null,"sp":"162","vol":"13","edition":null,"conferencePlace":null,"conferenceDate":null},"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"doi_________::7eab46c26a2b77cf994984ed167e2589","originalIds":["10.33263/briac132.162","50|doiboost____|7eab46c26a2b77cf994984ed167e2589"],"pids":[{"scheme":"doi","value":"10.33263/briac132.162"}],"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":2,"influence":2.6084284e-9,"popularity":3.4074417e-9,"impulse":2,"citationClass":"C5","influenceClass":"C5","impulseClass":"C5","popularityClass":"C5"}},"instances":[{"pids":[{"scheme":"doi","value":"10.33263/briac132.162"}],"type":"Article","urls":["https://doi.org/10.33263/briac132.162"],"publicationDate":"2022-03-29","refereed":"peerReviewed"}],"isGreen":false,"isInDiamondJournal":false}
local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus

Dosyalar

Koleksiyonlar