An in-situ route for the fabrication of intramol. electron donor-acceptor (D-A) structured g-C3N4 photocatalysts is developed by the preorganization of urea with the precursor of electron donor units, such as 4-iodobenzaldehyde, 5-bromo-2-thiophenaldehyde and 5-bromo-2-furaldehyde, followed by thermal polymerizationIn the resulting benzene unit-, thiophene unit- and furan unit-based D-A structured g-C3N4 photocatalysts, namely, BHCNx, SCNx, and OCNx, the incorporated electron donor units (i.e., benzene units, thiophene units and furan units) link with the electron acceptors (i.e., heptazine units) through C-N and C=N covalent bonds.In comparison of bulk g-C3N4, all D-A structured g-C3N4 display notably enhanced visible-light photocatalytic oxidation activity in the degradation of emerging organic micropollutants, p-nitrophenol (PNP) and methylparaben (MPB), in which the apparent first-order kinetic constant of the optimized BHCN2, SCN2, and OCN2 is 1.6, 3.0 and 6.8 times higher than bulk g-C3N4 for PNP degradation and 1.9, 3.4 and 2.6 times higher than bulk g-C3N4 for MPB degradationImportantly, the micropollutants can be not only degraded but also mineralized completely.The catalysts are also robust in the removal of mixed emerging organic micropollutants in pharmaceutical wastewater, exhibiting potential of dealing with organic micropollutants in wastewater.Mechanism studies reveal that the unique intramol. charge transfer process in the catalysts enhances visible-light harvesting capacity, boosts directional transfer of the photogenerated charges and increases adsorption towards oxygen mols.These collective improvements can maximum utilization the photogenerated electrons and holes to yield plentiful reactive oxygen species for deep oxidization of the pollutants.