دورية أكاديمية
Bilirubin analogues as model compounds for exciton coupling.
العنوان: | Bilirubin analogues as model compounds for exciton coupling. |
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المؤلفون: | Lyskov I; ARC Centre of Excellence in Exciton Science, Australia., Anda A, Wong YX, Tilley AJ, Hall CR, Thia J, Russo SP, Wong WWH, Cole JH, Smith TA |
المصدر: | Physical chemistry chemical physics : PCCP [Phys Chem Chem Phys] 2020 Jul 21; Vol. 22 (27), pp. 15567-15572. Date of Electronic Publication: 2020 Jul 02. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 100888160 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1463-9084 (Electronic) Linking ISSN: 14639076 NLM ISO Abbreviation: Phys Chem Chem Phys Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: Cambridge [England] : Royal Society of Chemistry, c1999- |
مواضيع طبية MeSH: | Density Functional Theory*, Antioxidants/*chemistry , Bilirubin/*chemistry, Antioxidants/chemical synthesis ; Bilirubin/analogs & derivatives ; Bilirubin/chemical synthesis ; Molecular Structure ; Static Electricity |
مستخلص: | A series of phycobilin analogues have been investigated in terms of coupled excitonic systems. These compounds consist of a monomer, a tetrapyrrole structurally similar to bilirubin (bR), and two conjugated bR analogues. Spectroscopic and computational methods have been used to investigate the degree of interchromophore coupling. We find the synthesised bR analogue shows stronger excitonic coupling than bR, owing to a different molecular geometry. The excitonic coupling in the conjugated molecules can be controlled by modifying the bridge side-group. New computed energy levels for bR using the DFT/MRCI method are also presented, which improve on published values and re-assign the character of excited singlet states. |
المشرفين على المادة: | 0 (Antioxidants) RFM9X3LJ49 (Bilirubin) |
تواريخ الأحداث: | Date Created: 20200703 Date Completed: 20201208 Latest Revision: 20201214 |
رمز التحديث: | 20240829 |
DOI: | 10.1039/d0cp01421d |
PMID: | 32613218 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1463-9084 |
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DOI: | 10.1039/d0cp01421d |