A new carbazole-based 90° dipyridyl donor 3,6-di(4-pyridylethynyl) carbazole (L) containing carbazole-ethynyl functionality is synthesized in reasonable yield using the Sonagashira coupling reaction. Multinuclear NMR, electrospray ionization-mass spectrometry (ESI-MS), including single crystal X-ray diffraction analysis characterized this 90° building unit. The stoichiometry combination of L with several Pd(II)/Pt(II)-based 90° acceptors (1a-1d) yielded [2 + 2] self-assembled metallacycles (2a-2d) under mild conditions in quantitative yields [1a = cis-(dppf)Pd(OTf) 2; 1b = cis-(dppf)Pt(OTf) 2; 1c = cis-(tmen)Pd(NO 3) 2; 1d = 3,6-bis{trans-Pt(C=C)(PEt 3) 2(NO 3)} carbazole]. All these macrocycles were characterized by various spectroscopic techniques, and the molecular structure of 2a was unambiguously determined by single crystal X-ray diffraction analysis. Incorporation of ethynyl functionality to the carbazole backbone causes the resulted macrocycles (2a-2d) to be π-electron rich and thereby exhibit strong emission characteristics. The macrocycle 2a has a large internal concave aromatic surface. The fluorescence quenching study suggests that 2a forms a ∼1:1 complex with C 60 with a high association constant of K sv = 1.0 × 10 5 M -1. © 2012 American Chemical Society.