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ÏëÖªµÀ£¬CdSe−CdS£¨¸øÌ壩/»¨ÇàËØÈ¾ÁÏ£¨ÊÜÌ壩×é³ÉµÄFRETÌåϵ£¬ÓÃÕâ¸öÌåϵÄܲâÁ¿Î¶ȣ¬²âÁ¿µÄÐźÅʱ˫·¢ÉäÐźţ¿Ô­ÀíÊÇʲô£¿¼ÈÈ»»¨ÇàËØºÍCdSe−CdSµÄÓ«¹â¶ÔÈȶ¼Ãô¸Ð£¬ÎªÊ²Ã´·ÇÒª×é³É¸öFRET£¿ÕâÀïµÄË«·¢ÉäÓÐÊ²Ã´ÌØµã¼°Óŵ㣿£¨J. Am. Chem. Soc. 2012, 134, 9565−9568£©

We show here that hybrid nanomaterials based on polymerwrapped
CdSe−CdS quantum dot−quantum rod (QD−QRs)
functionalized with temperature-responsive cyanine dyes
address these issues in a single construct and exhibit enhanced
thermometric response and sensitivity when translocated to the
cytosol. By modeling optical changes in the nanocrystals
components as a function of temperature, we find that response
of this construct is also well explained by the change in
quantum yield of the CdSe−CdS QD−QRs versus the cyanine
dye and the red shift in QD−QR emission with increasing
temperature.
The molecular design of dual-emitting ratiometric nanothermometers
(NanoTs) features a red-emitting CdSe−CdS
QD−QR semiconductor nanocrystal heterostructure passivated
with an amphiphilic polymer shell, to which is appended far-red
emitting cyanine dyes (Scheme 1). QD−QRs have giant
extinction coefficients9 owing to their CdS shells, and bright
temperature-responsive luminescence due to well-behaved
shifts in their bandgap (Figure S2). Cyanine dyes10 (e.g.,
Alexa Fluor 647), on the other hand, show temperaturedependent
fluorescence quantum yields but no wavelength
shifts (Figure S3). Together, they constitute FRET pairs with
thermoresponsive character ideal for ratiometric imaging: their
internally calibrated, strong optical read-out should translate to more reliable and precise temperature measurements in cells
than is possible otherwise using conventional FRET donors like
quantum dots, which are at least an order of magnitude less
bright than QD−QRs.
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