Abstract
Novel bridged phthalein dyes substituted with a diisopropylamide ortho to the bridge are stable at high pH; with a chromogenically active auxochrome ortho to the meso carbon, a hypsochromic shift, band narrowing, and an increased molar absorptivity of the near-infrared absorbance are observed relative to the regioisomer in which the chromogenically active auxochrome is para.
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