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Rational design of near-infrared (NIR) absorbing molecules is crucial for developing photofunctional materials. Here, we synthesized dinuclear and mononuclear Re(i) tricarbonyl phthalocyanine complexes that exhibit a sharp intense Q band in the NIR region. The unsymmetric coordination of electron-deficient metal unit(s) concomitantly produced a remarkable red shift of the Q band and improved the tolerance of the phthalocyanine ring to oxidation. This study presents a simple and effective strategy for the construction of NIR absorbers with
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