Results of x-ray powder diffraction and magnetic measurements performed on compounds, where Ho, Er, and Lu, are presented. The Curie temperature, saturation magnetization, and spin reorientation transitions are discussed in relation to several systems, where Nb, Mo, Ti, and the x-substituent concentration is within a narrow range In these systems, the dependence of the Curie temperature versus the unit cell volume, for a given R partner, suggests combined size and electronic effects produced by the T atom. The strengths of the rare-earth–iron and iron-iron exchange interactions are evaluated in the mean-field framework, and analyzed with reference to compounds, with Re, Nb, Mo, Ti, Cr, and V. Based on (i) the phenomenological mean-field model accounting for the sublattice of conduction band electrons, (ii) Brooks’ reinterpretation of Campbell’s formulation of the intersublattice exchange, and (iii) Wigner-Seitz cell analysis, we explore the role played by the conduction band electrons, particularly the nd-type electrons 4, 5), on the intersublattice exchange coupling in the iron-rich class of compounds. It is proposed that the variation in the conduction-electron density, by varying the T element type and concentration, leads to a modification of the band occupancy number and consequently, of the R-Fe intersublattice exchange coupling.