M.B. Murphy

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Name:
Organization: City University of Hong Kong , HongKong
Department: Department of Biology and Chemistry
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Wanqing Wu;Hoi-Kuan Kong;Hongguang Li;Yu-Man Ho;Yuan Gao;Jianhua Hao;Margaret B. Murphy;Michael Hon-Wah Lam;Ka-Leung Wong;Chi-Sing Lee
European Journal of Organic Chemistry 2011 Volume 2011( Issue 26) pp:5054-5060
Publication Date(Web):
DOI:10.1002/ejoc.201100570

Abstract

A new class of organic molecular probes (13) based on a 1,3-disubstituted diethynylbenzene core has been developed. Both 1 and 2 (with the esters of 1 replaced by diethylamides in 2) show good linear and three-photon induced photophysical properties with two-photon absorption cross-sections (185–210 cm4 s photon–1 molecule–1) that are suitable for biological applications in live specimens. The propeller π-conjugated systems of 3 (a C3 analogue of 1) shows threefold enhancement for the two-photon absorption cross-section (650 cm4 s photon–1 molecule–1). Solvatochromism was observed in the fluorescence spectra of all these molecular probes; in acidic medium (pH = 4–5) their fluorescence emissions are slightly blueshifted with a threefold enhancement in intensity relative to those observed under basic conditions (pH = 10–11). In the fluorometric titration study against a variety of bioactive small molecules, only 2 shows strong binding affinity (log KB > 7) towards citrates and bicarbonates with approximately 30 nm redshift. The in vitro emission spectra of 2 obtained show the same emission upon addition of anions to the solution. The results of these studies could provide new molecular-design strategies for two-photo absorption (TPA) chromophores and new materials for two/multi-photon imaging in vitro.

Co-reporter:H.W. Leung, T.B. Minh, M.B. Murphy, James C.W. Lam, M.K. So, Michael Martin, Paul K.S. Lam, B.J. Richardson
Environment International (July 2012) Volume 42() pp:1-9
Publication Date(Web):1 July 2012
DOI:10.1016/j.envint.2011.03.004
Occurrence, removal, consumption and environmental risks of sixteen antibiotics were investigated in several sewage treatment plants (STPs) featuring different treatment levels in Hong Kong, China. Cefalexin, ofloxacin and erythromycin-H2O were predominant with concentrations of 1020–5640, 142–7900 and 243–4740 ng/L in influent, respectively; their mass loads were comparable to levels reported in urban regions in China and were at the high end of the range reported for western countries. The target antibiotics behaved differently depending on the treatment level employed at the STPs and relatively higher removal efficiencies (> 70%) were observed for cefalexin, cefotaxime, amoxicillin, sulfamethoxazole and chloramphenicol during secondary treatment. ß-lactams were especially susceptible to removal via the activated sludge process while macrolides were recalcitrant (< 20%) in the dissolved phase. Two fluoroquinolones, ofloxacin (4%) and norfloxacin (52%), differed greatly in their removal efficiencies, probably because of disparities in their pKa values which resulted in different sorption behaviour in sludge. Overall antibiotic consumption in Hong Kong was back-calculated based on influent mass flows and compared with available prescription and usage data. This model was verified by a good approximation of 82% and 141% to the predicted consumption of total ofloxacin, but a less accurate estimate was obtained for erythromycin usage. Risk assessment indicated that algae are susceptible to the environmental concentrations of amoxicillin as well as the mixture of the nine detected antibiotics in receiving surface waters.Research Highlights► Sixteen antibiotics quantified in sewage treatment plants in Hong Kong. ► Cefalexin, ofloxacin and erythromycin-H2O were predominant in influent. ► Higher removal efficiencies of some antibiotics after secondary treatment. ► Amoxicillin and a mixture of nine detected antibiotics may pose a risk to algae.
Benzene, 1,5-dibromo-2-(2,4-dibromophenoxy)-4-methoxy-
Benzene, 4-bromo-1-(2,4-dibromophenoxy)-2-methoxy-
Phenol, 3-chloro-2-(2,4-dibromophenoxy)-
1-Propyne, 3-[2,2,2-trifluoro-1,1-bis(trifluoromethyl)ethoxy]-
Benzene, 2-bromo-1-(2,4-dibromophenoxy)-4-methoxy-
Phenol, 5-bromo-2-(2,4-dibromophenoxy)-
PHENOL, 4,6-DIBROMO-3-CHLORO-2-(2,4-DIBROMOPHENOXY)-
BENZENE, 1,5-DIBROMO-2-CHLORO-3-(2,4-DIBROMOPHENOXY)-4-METHOXY-
PHENOL, 2-(2,4-DIBROMOPHENOXY)-
1-PROPANESULFONIC ACID, 1,1,2,2,3,3,3-HEPTAFLUORO-