Aqueous solutions of poly(methacrylic acid)-b-polydimethylsiloxane copolymer (PMA-b-PDMS), and reference solutions of PMA homopolymer, were studied as a function of pH using fluorescent probes: pyrene (P) and 1,3-bis(1-pyrenyl)propane (P3P). In both polymers the conformational transition of PMA chains at PH > 5 was reflected in the sharp increase of the intensity ratio of the first to the third vibronic band in emission spectra of P; an excimer emission appeared for P3P, as well as for P if the probe concentration was higher than its solubility limit in water. The excimer to monomer intensity ratio of both probes is a sensitive indicator of the conformational transitions of polymer chains, but P3P is significantly more sensitive compared to pyrene. The data clearly indicated that the presence of PDMS blocks markedly facilitated the transition, even though the ratio of dimethylsiloxane to methacrylic acid units in the copolymer was low, 1:34. The absence of the P3P excimer emission at PH approximate to 3 was rationalized by assuming that clustering of sections of PMA chains around pyrene moieties imposes an extended conformation of the probe molecule. (C) 2004 Elsevier Ltd. All rights reserved.