Atomically precise, δ-doped structures forming electronic devices in Si have been routinely fabricated in recent years by using depassivation lithography in a scanning tunneling microscope (STM). While H-based precursor/monatomic resist chemistries for incorporation of donor atoms have dominated these efforts, the use of halogen-based chemistries offers a promising path toward atomic-scale manufacturing of acceptor-based devices. Here, B-doped δ-layers were fabricated in Si(100) by using BCl 3 as an acceptor dopant precursor in ultrahigh vacuum. Additionally, we demonstrate compatibility of BCl 3 with both H and Cl monatomic resists to achieve area-selective deposition on Si. In comparison to bare Si, BCl 3 adsorption selectivity ratios for H-and Cl-passivated Si were determined by secondary ion mass spectrometry depth profiling (SIMS) to be 310(10):1 and 1529(5):1, respectively. STM imaging revealed that BCl 3 adsorbed readily on bare Si at room temperature, with SIMS measurements indicating a peak B concentration greater than 1.2(1) × 10 21 cm −3 with a total areal dose of 1.85(1) × 10 14 cm −2 resulting from a 30 langmuir BCl 3 dose at 150 °C. In addition, SIMS showed a δ-layer thickness of ∼0.5 nm. Hall bar measurements of a similar sample were performed at 3.0 K, revealing a sheet resistance of ρ □ = 1.9099(4) kΩ □ −1 , a hole carrier concentration of p = 1.90(2) × 10 14 cm −2 , and a hole mobility of μ = 38.0(4) cm 2 V −1 s −1 without performing an incorporation anneal. Finally, 15 nm wide B δ-doped nanowires were fabricated from BCl 3 and were found to exhibit ohmic conduction. This validates the use of BCl 3 as a dopant precursor for atomicprecision fabrication of acceptor-doped devices in Si and enables development of simultaneous n-and p-type doped bipolar devices.