X-ray Crystal Structure and Time-Resolved Spectroscopy of the Blue Carotenoid Violerythrin

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12640%2F10%3A00012169" target="_blank" >RIV/60076658:12640/10:00012169 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/60077344:_____/10:00355275

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

X-ray Crystal Structure and Time-Resolved Spectroscopy of the Blue Carotenoid Violerythrin

Popis výsledku v původním jazyce

Violerythrin, a blue-colored carotenoid, has been investigated by X-ray crystallography and steady-state and ultrafast time-resolved absorption spectroscopy. The X-ray crystal structure of violerythrin shows that the molecule is nearly planar with the terminal rings positioned in the s-trans conformation. The steady-state and time-resolved spectroscopic data of violerythrin do not differ significantly from those of other carbonyl carotenoids with long (N > 10) pi-electron conjugated chains. This indicates that while the four carbonyl groups in violerythrin are critical for generating the bathochromic shift that leads to the blue color of the molecule, no dramatic changes attributable to a charge-transfer state known to affect the excited-state properties of carotenoids with short polyene chains occur. This may be due to the symmetric distribution of the carbonyl groups, which would preclude such an effect. The structural requirements for a blue, neutral, carotenoid are a planar, symmet

Název v anglickém jazyce

X-ray Crystal Structure and Time-Resolved Spectroscopy of the Blue Carotenoid Violerythrin

Popis výsledku anglicky

Violerythrin, a blue-colored carotenoid, has been investigated by X-ray crystallography and steady-state and ultrafast time-resolved absorption spectroscopy. The X-ray crystal structure of violerythrin shows that the molecule is nearly planar with the terminal rings positioned in the s-trans conformation. The steady-state and time-resolved spectroscopic data of violerythrin do not differ significantly from those of other carbonyl carotenoids with long (N > 10) pi-electron conjugated chains. This indicates that while the four carbonyl groups in violerythrin are critical for generating the bathochromic shift that leads to the blue color of the molecule, no dramatic changes attributable to a charge-transfer state known to affect the excited-state properties of carotenoids with short polyene chains occur. This may be due to the symmetric distribution of the carbonyl groups, which would preclude such an effect. The structural requirements for a blue, neutral, carotenoid are a planar, symmet

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

BO - Biofyzika

OECD FORD obor

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Projekt

<a href="/cs/project/ME09037" target="_blank" >ME09037: Excitované stavy karbonylových karotenoidů a jejich role ve fotochemických reakcích</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2010

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Physical Chemistry B

ISSN

1520-6106

e-ISSN

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Svazek periodika

114

Číslo periodika v rámci svazku

26

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

10

Strana od-do

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Kód UT WoS článku

000279282600021

EID výsledku v databázi Scopus

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