<P>From kinetic experiments monitoring the consumption of chalcogenide precursors by <SUP>31</SUP>P NMR, it could be concluded that the formation rates of metal chalcogenides (M–E, M = Cd or Zn and E = Se or S) were in the orde...
http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
https://www.riss.kr/link?id=A107753032
2012
-
학술저널
10827-10833(7쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>From kinetic experiments monitoring the consumption of chalcogenide precursors by <SUP>31</SUP>P NMR, it could be concluded that the formation rates of metal chalcogenides (M–E, M = Cd or Zn and E = Se or S) were in the orde...
<P>From kinetic experiments monitoring the consumption of chalcogenide precursors by <SUP>31</SUP>P NMR, it could be concluded that the formation rates of metal chalcogenides (M–E, M = Cd or Zn and E = Se or S) were in the order of ZnS < ZnSe < CdS < CdSe when one equivalent of metal oleate (M–OA) precursor reacted with one equivalent of trioctylphosphine chalcogenide (TOP–E) precursor. On the basis of the reactivity differences, various amounts of each precursor molecule could be deliberately chosen to tune the structure of the generated QDs and consequently the emission colors in the entire visible range. The excellent photochemical stability of the gradient alloy QDs could provide evidence that a good overall coverage of the shell on the core part significantly reduced defects due to lattice mismatch.</P>
<P>Graphic Abstract</P><P>From kinetic experiments monitoring the consumption of chalcogenide precursors by <SUP>31</SUP>P NMR, it could be concluded that the formation rates of metal chalcogenides (M–E, M = Cd or Zn and E = Se or S) were in the order of ZnS < ZnSe < CdS < CdSe when one equivalent of metal oleate (M–OA) precursor reacted with one equivalent of trioctylphosphine chalcogenide (TOP–E) precursor.
<IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c2jm16448e'>
</P>
Amphiphilic hyaluronic acid-based nanoparticles for tumor-specific optical/MR dual imaging