Self-Assembly of Fluorescent Inclusion Complexes in Competitive Media Including the Interior of Living Cells
journal contributionposted on 05.12.2007, 00:00 by Jeremiah J. Gassensmith, Easwaran Arunkumar, Lorna Barr, Jeffrey M. Baumes, Kristy M. DiVittorio, James R. Johnson, Bruce C. Noll, Bradley D. Smith
Anthracene-containing tetralactam macrocycles are prepared and found to have an extremely high affinity for squaraine dyes in chloroform (log Ka = 5.2). Simply mixing the two components produces highly fluorescent, near-infrared inclusion complexes in quantitative yield. An X-ray crystal structure shows the expected hydrogen bonding between the squaraine oxygens and the macrocycle amide NH residues, and a high degree of cofacial aromatic stacking. The kinetics and thermodynamics of the assembly process are very sensitive to small structural changes in the binding partners. For example, a macrocycle containing two isophthalamide units associates with the squaraine dye in chloroform 400 000 times faster than an analogous macrocycle containing two 2,6-dicarboxamidopyridine units. Squaraine encapsulation also occurs in highly competitive media such as mixed aqueous/organic solutions, vesicle membranes, and the organelles within living cells. The highly fluorescent inclusion complexes possess emergent properties; that is, as compared to the building blocks, the complexes have improved chemical stabilities, red-shifted absorption/emission maxima, and different cell localization propensities. These are useful properties for new classes of near-infrared fluorescent imaging probes.
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squaraine dyesinclusion complexesCompetitive Mediaassembly processsquaraine dyemacrocycle amide NH residuesSquaraine encapsulationsquaraine oxygensvesicle membranesisophthalamide units associatesbuilding blockschloroform 400 000 timeslog Kaimaging probescell localization propensitiesbinding partners400 000Fluorescent Inclusion Complexeschemical stabilities