東華大學圖書館 |

Language: English

Help

回圖書館首頁

手機版館藏查詢

Back

Switch To: Labeled | MARC Mode | ISBD

The application of fluorescent speci...

Boston University.

Linked to FindBook

Google Book

Amazon

博客來

The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection.

Record Type:	Electronic resources : Monograph/item
Title/Author:	The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection./
Author:	Xia, Bing.
Description:	242 p.
Notes:	Adviser: Guilford Jones, II.
Contained By:	Dissertation Abstracts International69-10B.
Subject:	Chemistry, Analytical. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3334566
ISBN:	9780549874300

The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection.
Xia, Bing.

The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection. - 242 p.

Adviser: Guilford Jones, II.

Thesis (Ph.D.)--Boston University, 2009.

This dissertation concerns the application of photochemistry in the synthesis of novel tricyclic structures which are analogues of alkaloids. The photophysical studies focused on the unusual mechanism of excited state intramolecular proton transfer (ESIPT). The previously reported ESIPT of a 3-hydroxyflavone (3HF) derivative and the [3+2] dipolar cycloaddition of the resulting oxidopyryllium species with methyl cinnamate inspired extension of the study to aza-analogues of 3HF. Irradiation of 1,2-dimethyl-3-hydroxyquinolinone (DMQ) led to the induced ESIPT product, a 3-oxidoquinolinium species that was, in turn, trapped by [3+2] dipolar cycloaddition with a series of dipolarophiles to give tricyclic (alkaloid-like) products. Photophysical studies were employed to establish a relationship between synthetic reactivity and the rate constant (kq) for quenching of quinolinone fluorescence by dipolarophiles. An efficient method for predicting reactivity resulted from the study, along with procedures for access to novel alkaloid derivatives having challenging structural features.

ISBN: 9780549874300Subjects--Topical Terms:

586156
Chemistry, Analytical.

The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection.
LDR:02874nmm 2200301 a 45 001 862858
005 20100721
008 100721s2009 ||||||||||||||||| ||eng d
020 $a 9780549874300
035 $a (UMI)AAI3334566
035 $a AAI3334566
040 $a UMI $c UMI
100 1 $a Xia, Bing. $3 1030722
245 1 4 $a The application of fluorescent species and their interactions for the development of methods in synthesis and biodetection.
300 $a 242 p.
500 $a Adviser: Guilford Jones, II.
500 $a Source: Dissertation Abstracts International, Volume: 69-10, Section: B, page: 6117.
502 $a Thesis (Ph.D.)--Boston University, 2009.
520 $a This dissertation concerns the application of photochemistry in the synthesis of novel tricyclic structures which are analogues of alkaloids. The photophysical studies focused on the unusual mechanism of excited state intramolecular proton transfer (ESIPT). The previously reported ESIPT of a 3-hydroxyflavone (3HF) derivative and the [3+2] dipolar cycloaddition of the resulting oxidopyryllium species with methyl cinnamate inspired extension of the study to aza-analogues of 3HF. Irradiation of 1,2-dimethyl-3-hydroxyquinolinone (DMQ) led to the induced ESIPT product, a 3-oxidoquinolinium species that was, in turn, trapped by [3+2] dipolar cycloaddition with a series of dipolarophiles to give tricyclic (alkaloid-like) products. Photophysical studies were employed to establish a relationship between synthetic reactivity and the rate constant (kq) for quenching of quinolinone fluorescence by dipolarophiles. An efficient method for predicting reactivity resulted from the study, along with procedures for access to novel alkaloid derivatives having challenging structural features.
520 $a Sensitive and simple bioanalytical methods for rapid quantitative detection of potential biohazards are now required in a number of venues, such as biodefense, environmental monitoring, food processing and microbiological settings. In the second part of this dissertation, the characteristic spectroscopic signature for interaction of thioflavin T (TfT) with suspended bacterial endospores was studied. A fluorescent reporter library was designed and synthesized by a newly developed route using TfT as the lead compound. Besides information regarding structure-activity relationships (SAR), specific spectroscopic reactivity toward important classes of potential bioharzards including not only dormant bacterial spores, but also vegetative bacterial cells, has been achieved employing this panel of fluorescent probes.
590 $a School code: 0017.
650 4 $a Chemistry, Analytical. $3 586156
650 4 $a Chemistry, Organic. $3 516206
650 4 $a Chemistry, Physical. $3 560527
690 $a 0486
690 $a 0490
690 $a 0494
710 2 $a Boston University. $3 1017454
773 0 $t Dissertation Abstracts International $g 69-10B.
790 $a 0017
790 1 0 $a Jones, Guilford, II, $e advisor
791 $a Ph.D.
792 $a 2009
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3334566