Rowan Molecule Handling Reference

Rowan Molecule Handling Reference

Overview

Rowan uses the stjames library for molecular representations. The stjames.Molecule class provides a unified interface for creating molecules from various sources and accessing molecular properties.

Table of Contents

1. Creating Molecules
2. Molecule Attributes
3. Geometry Methods
4. File I/O
5. Conversion Functions
6. Working with Atoms

Creating Molecules

From SMILES

import stjames

# Simple SMILES
mol = stjames.Molecule.from_smiles("CCO")  # Ethanol
mol = stjames.Molecule.from_smiles("c1ccccc1")  # Benzene

# With stereochemistry
mol = stjames.Molecule.from_smiles("C[C@H](O)[C@@H](O)C")  # meso-2,3-butanediol

# Charged molecules
mol = stjames.Molecule.from_smiles("[NH4+]")  # Ammonium
mol = stjames.Molecule.from_smiles("CC(=O)[O-]")  # Acetate

# Complex drug-like molecules
mol = stjames.Molecule.from_smiles("CC(=O)Oc1ccccc1C(=O)O")  # Aspirin

Note: from_smiles() automatically generates 3D coordinates.

From XYZ String

import stjames

xyz_string = """3
Water molecule
O  0.000  0.000  0.117
H  0.000  0.757 -0.469
H  0.000 -0.757 -0.469"""

mol = stjames.Molecule.from_xyz(xyz_string)

XYZ format with optional metadata in comment line:

N_atoms
charge=0 multiplicity=1 energy=-76.4 comment
Element X Y Z
...

From XYZ File

import stjames

mol = stjames.Molecule.from_file("structure.xyz")

From Extended XYZ (EXTXYZ)

Extended XYZ supports additional properties like forces and cell parameters.

import stjames

extxyz_string = """3
Lattice="10.0 0.0 0.0 0.0 10.0 0.0 0.0 0.0 10.0" Properties=species:S:1:pos:R:3:forces:R:3 energy=-76.4
O  0.000  0.000  0.117  0.01 0.02 0.03
H  0.000  0.757 -0.469  0.00 0.00 0.00
H  0.000 -0.757 -0.469  0.00 0.00 0.00"""

mol = stjames.Molecule.from_extxyz(extxyz_string)

# Access cell information
if mol.cell:
    print(f"Cell: {mol.cell.lattice_vectors}")

From RDKit Molecule

import stjames
from rdkit import Chem
from rdkit.Chem import AllChem

# Create RDKit molecule with 3D coordinates
rdkit_mol = Chem.MolFromSmiles("CCO")
rdkit_mol = Chem.AddHs(rdkit_mol)
AllChem.EmbedMolecule(rdkit_mol)
AllChem.MMFFOptimizeMolecule(rdkit_mol)

# Convert to stjames
mol = stjames.Molecule.from_rdkit(rdkit_mol)

Specifying Charge and Multiplicity

import stjames

# Neutral singlet (default)
mol = stjames.Molecule.from_smiles("CCO")

# Cation doublet
mol = stjames.Molecule.from_smiles("CCO", charge=1, multiplicity=2)

# Anion singlet
mol = stjames.Molecule.from_smiles("CC(=O)[O-]", charge=-1, multiplicity=1)

# Triplet oxygen
mol = stjames.Molecule.from_smiles("[O][O]", charge=0, multiplicity=3)

Molecule Attributes

Basic Properties

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Charge and spin
print(f"Charge: {mol.charge}")  # 0
print(f"Multiplicity: {mol.multiplicity}")  # 1

# Number of atoms
print(f"Number of atoms: {len(mol.atoms)}")

Computed Properties (after calculation)

# After running a calculation
print(f"Energy: {mol.energy} Hartree")
print(f"Dipole: {mol.dipole}")  # (x, y, z) in Debye

# Atomic properties
print(f"Mulliken charges: {mol.mulliken_charges}")
print(f"Mulliken spin densities: {mol.mulliken_spin_densities}")

Thermochemistry (after frequency calculation)

# After frequency calculation
print(f"ZPE: {mol.zero_point_energy} Hartree")
print(f"Thermal correction to enthalpy: {mol.thermal_correction_enthalpy}")
print(f"Thermal correction to Gibbs: {mol.thermal_correction_gibbs}")
print(f"Gibbs free energy: {mol.gibbs_free_energy} Hartree")

Vibrational Modes (after frequency calculation)

for mode in mol.vibrational_modes:
    print(f"Frequency: {mode.frequency} cm⁻¹")
    print(f"Reduced mass: {mode.reduced_mass} amu")
    print(f"IR intensity: {mode.ir_intensity} km/mol")
    print(f"Displacements: {mode.displacements}")

Periodic Cell

if mol.cell:
    print(f"Lattice vectors: {mol.cell.lattice_vectors}")
    print(f"Is periodic: True")

Geometry Methods

Distance Between Atoms

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Distance between atoms 0 and 1 (in Angstroms)
d = mol.distance(0, 1)
print(f"C-C bond length: {d:.3f} Å")

Angle Between Three Atoms

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Angle formed by atoms 0-1-2 (C-C-O)
angle = mol.angle(0, 1, 2, degrees=True)
print(f"C-C-O angle: {angle:.1f}°")

# In radians
angle_rad = mol.angle(0, 1, 2, degrees=False)

Dihedral Angle

import stjames

mol = stjames.Molecule.from_smiles("CCCC")

# Dihedral angle for atoms 0-1-2-3
dihedral = mol.dihedral(0, 1, 2, 3, degrees=True)
print(f"Dihedral: {dihedral:.1f}°")

# Use positive domain (0 to 360)
dihedral_pos = mol.dihedral(0, 1, 2, 3, degrees=True, positive_domain=True)

Translation

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Translate by vector
translated = mol.translated([1.0, 0.0, 0.0])  # Move 1 Å in x direction

File I/O

Export to XYZ

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Get XYZ string
xyz_str = mol.to_xyz(comment="Ethanol optimized structure")
print(xyz_str)

# Write to file
mol.to_xyz(comment="Ethanol", out_file="ethanol.xyz")

Export to Extended XYZ

import stjames

mol = stjames.Molecule.from_smiles("CCO")

# Include energy in comment
xyz_str = mol.to_xyz(comment=f"energy={mol.energy}")

Conversion Functions

SMILES to Molecule (Rowan Utility)

import rowan

# Quick conversion using Rowan's utility
mol = rowan.smiles_to_stjames("CCO")

Molecule Lookup by Name

import rowan

# Convert common names to SMILES
smiles = rowan.molecule_lookup("aspirin")
print(smiles)  # "CC(=O)Oc1ccccc1C(=O)O"

smiles = rowan.molecule_lookup("caffeine")
print(smiles)  # "Cn1cnc2c1c(=O)n(c(=O)n2C)C"

# Use with workflow submission
mol = stjames.Molecule.from_smiles(rowan.molecule_lookup("ibuprofen"))
workflow = rowan.submit_pka_workflow(mol, name="Ibuprofen pKa")

Working with Atoms

Atom Class

Each atom in mol.atoms is an Atom object.

import stjames

mol = stjames.Molecule.from_smiles("CCO")

for i, atom in enumerate(mol.atoms):
    print(f"Atom {i}: {atom.element}")
    print(f"  Position: ({atom.x:.3f}, {atom.y:.3f}, {atom.z:.3f})")

Atom Attributes

Getting Coordinates as Array

import stjames
import numpy as np

mol = stjames.Molecule.from_smiles("CCO")

# Extract positions as numpy array
positions = np.array([[atom.x, atom.y, atom.z] for atom in mol.atoms])
print(f"Positions shape: {positions.shape}")  # (N_atoms, 3)

Common Patterns

Batch Molecule Creation

import stjames

smiles_list = ["CCO", "CC(=O)O", "c1ccccc1", "c1ccccc1O"]

molecules = []
for smi in smiles_list:
    try:
        mol = stjames.Molecule.from_smiles(smi)
        molecules.append(mol)
    except Exception as e:
        print(f"Failed to create molecule from {smi}: {e}")

print(f"Created {len(molecules)} molecules")

Modifying Charge/Multiplicity

import stjames

# Create neutral molecule
mol = stjames.Molecule.from_smiles("c1ccccc1")

# Create cation version
mol_cation = stjames.Molecule.from_smiles("c1ccccc1", charge=1, multiplicity=2)

# Or modify existing (if supported)
# Note: May need to recreate from coordinates

Combining Geometry Analysis

import stjames

mol = stjames.Molecule.from_smiles("CCCC")

# Analyze butane conformer
print("Butane geometry analysis:")
print(f"  C1-C2 bond: {mol.distance(0, 1):.3f} Å")
print(f"  C2-C3 bond: {mol.distance(1, 2):.3f} Å")
print(f"  C3-C4 bond: {mol.distance(2, 3):.3f} Å")
print(f"  C-C-C angle: {mol.angle(0, 1, 2, degrees=True):.1f}°")
print(f"  C-C-C-C dihedral: {mol.dihedral(0, 1, 2, 3, degrees=True):.1f}°")

Electron Sanity Check

The stjames.Molecule class validates that charge and multiplicity are consistent with the number of electrons:

import stjames

# This will fail validation
try:
    # Oxygen with wrong multiplicity
    mol = stjames.Molecule.from_smiles("[O][O]", charge=0, multiplicity=1)
except ValueError as e:
    print(f"Validation error: {e}")

# Correct: triplet oxygen
mol = stjames.Molecule.from_smiles("[O][O]", charge=0, multiplicity=3)

The validation ensures:

• Number of electrons = sum(atomic_numbers) - charge
• Multiplicity is compatible with electron count (odd/even)