The preparation of multifunctionalized luminophores with full‐color emission based on an identical core skeleton is a significative but challenging research topic. In this work, eight donor‐donor‐acceptor (D‐D‐A)‐type luminogens based on a central carbazole core bearing a C6 hydrocarbon chain were designed by using different kinds of donor and acceptor units on the left and right, and synthesized in good yields. These D‐D‐A carbazole derivatives display deep‐blue, sky‐blue, cyan, green, yellow‐green, yellow, orange and red fluorescence in the solid state, achieving full‐color emission covering the whole visible light range under UV light illumination. Notably, the dicyano‐functionalized triphenylamine‐containing carbazole derivative exhibits rare aggregation‐induced near‐infrared emission and red‐to‐near‐infrared mechano‐fluorochromism with high contrast beyond 100 nm. Furthermore, the red‐emissive luminogen can serve as a potential candidate for cell imaging and photodynamic therapy (PDT). This work not only provides reference for the construction of full‐color emissive systems but also opens a new avenue to the preparation of multifunctionalized luminophores capable of simultaneous application in near‐Infrared mechanical‐force sensors and PDT fields.