def test_set_pi_bonds():
ethene = Species(name='ethene',
charge=0,
mult=1,
atoms=[
Atom('C', -2.20421, 0.40461, 0.00000),
Atom('C', -0.87115, 0.38845, 0.00000),
Atom('H', -2.76098, -0.22576, 0.68554),
Atom('H', -2.74554, 1.04829, -0.68554),
Atom('H', -0.32982, -0.25523, 0.68554),
Atom('H', -0.31437, 1.01882, -0.68554)
])
mol_graphs.make_graph(ethene)
assert ethene.graph.edges[0, 1]['pi'] is True
assert ethene.graph.edges[1, 0]['pi'] is True
assert ethene.graph.edges[0, 2]['pi'] is False
acetylene = Species(name='acetylene',
charge=0,
mult=1,
atoms=[
Atom('C', -2.14031, 0.40384, 0.00000),
Atom('C', -0.93505, 0.38923, 0.00000),
Atom('H', -3.19861, 0.41666, 0.00000),
Atom('H', 0.12326, 0.37640, 0.00000)
])
mol_graphs.make_graph(acetylene)
assert acetylene.graph.edges[0, 1]['pi'] is True
assert acetylene.graph.edges[0, 2]['pi'] is False
def test_species_isomorphism():
h2.graph = None
h2_copy = Species(name='H2', atoms=[h_a, h_b], charge=0, mult=1)
h2_copy.graph = None
with pytest.raises(NoMolecularGraph):
assert mol_graphs.species_are_isomorphic(h2, h2_copy)
# With molecular graphs the species should be isomorphic
mol_graphs.make_graph(h2)
mol_graphs.make_graph(h2_copy)
assert mol_graphs.species_are_isomorphic(h2, h2_copy)
# Shift one of the atoms far away and remake the graph
h2_copy.atoms[1].translate(vec=np.array([10, 0, 0]))
mol_graphs.make_graph(h2_copy)
assert mol_graphs.species_are_isomorphic(h2, h2_copy) is False
# Generating a pair of conformers that are isomporhpic should return that
# the species are again isomorphic
h2.conformers = [
Conformer(name='h2_conf', atoms=[h_a, h_b], charge=0, mult=1)
]
h2_copy.conformers = [
Conformer(name='h2_conf', atoms=[h_a, h_b], charge=0, mult=1)
]
assert mol_graphs.species_are_isomorphic(h2, h2_copy)
def test_species_class():
assert hasattr(mol, 'print_xyz_file')
assert hasattr(mol, 'translate')
assert hasattr(mol, 'rotate')
assert hasattr(mol, 'get_coordinates')
assert hasattr(mol, 'set_atoms')
assert hasattr(mol, 'set_coordinates')
assert mol.charge == 0
assert mol.mult == 1
assert mol.name == 'H2'
assert not mol.is_explicitly_solvated()
# A not very sensible water geometry!
water = Species(name='H2O',
charge=0,
mult=1,
atoms=[Atom('O'),
Atom('H', z=-1),
Atom('H', z=1)])
# Base class for molecules and TSs and complexes shouldn't have a
# implemented conformer method – needs to do different things based on the
# type of species to find conformers
with pytest.raises(NotImplementedError):
water.find_lowest_energy_conformer(lmethod=xtb)
def test_mapping():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.4)
h3_a = Species(name='template', charge=0, mult=1, atoms=[h_a, h_b, h_c])
mol_graphs.make_graph(species=h3_a, allow_invalid_valancies=True)
h3_b = Species(name='template', charge=0, mult=1, atoms=[h_a, h_b, h_c])
mol_graphs.make_graph(species=h3_b, allow_invalid_valancies=True)
# Isomorphic (identical) graphs should have at least one mapping between them
mapping = mol_graphs.get_mapping(h3_b.graph, h3_a.graph)
assert mapping is not None
assert type(mapping) == dict
def test_subgraph_isomorphism():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.4)
h_d = Atom(atomic_symbol='H', x=0.0, y=0.0, z=2.1)
h4 = Species(name='H4', atoms=[h_a, h_b, h_c, h_d], charge=0, mult=1)
mol_graphs.make_graph(h4)
assert mol_graphs.is_subgraph_isomorphic(larger_graph=h4.graph, smaller_graph=h2.graph) is True
# H3 in a triangular arrangement should not be sub-graph isomorphic to linear H4
h_e = Atom(atomic_symbol='H', x=0.3, y=0.0, z=0.3)
h3 = Species(name='H_H', charge=0, mult=1, atoms=[h_a, h_b, h_e])
mol_graphs.make_graph(h3, allow_invalid_valancies=True)
assert mol_graphs.is_subgraph_isomorphic(larger_graph=h4.graph, smaller_graph=h3.graph) is False
def test_species_copy():
species = Species(name='h', charge=0, mult=2, atoms=[Atom('H')])
species_copy = species.copy()
species_copy.charge = 1
assert species.charge != species_copy.charge
species_copy.mult = 3
assert species.mult != species_copy.mult
atom = species_copy.atoms[0]
atom.translate(vec=np.array([1.0, 1.0, 1.0]))
assert np.linalg.norm(species.atoms[0].coord - atom.coord) > 1
def test_not_isomorphic():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.0)
h2_b = Species(name='template', charge=0, mult=1, atoms=[h_a, h_c])
mol_graphs.make_graph(species=h2_b, rel_tolerance=0.3)
assert mol_graphs.is_isomorphic(h2.graph, h2_b.graph) is False
def test_not_isomorphic2():
c = Atom(atomic_symbol='C', x=0.0, y=0.0, z=0.7)
ch = Species(name='ch', atoms=[h_a, c], charge=0, mult=2)
mol_graphs.make_graph(ch)
assert mol_graphs.is_isomorphic(h2.graph, ch.graph) is False
def test_correct_imag_mode():
os.chdir(os.path.join(here, 'data'))
bond_rearrangement = BondRearrangement(breaking_bonds=[(4, 1), (4, 18)],
forming_bonds=[(1, 18)])
g09 = G09()
g09.available = True
calc = Calculation(name='tmp',
molecule=ReactantComplex(
Reactant(smiles='CC(C)(C)C1C=CC=C1')),
method=g09,
keywords=Config.G09.keywords.opt_ts)
calc.output.filename = 'correct_ts_mode_g09.log'
calc.output.set_lines()
f_displaced_atoms = get_displaced_atoms_along_mode(calc,
mode_number=6,
disp_magnitude=1.0)
f_species = Species(name='f_displaced',
atoms=f_displaced_atoms,
charge=0,
mult=1) # Charge & mult are placeholders
b_displaced_atoms = get_displaced_atoms_along_mode(calc,
mode_number=6,
disp_magnitude=-1.0)
b_species = Species(name='b_displaced',
atoms=b_displaced_atoms,
charge=0,
mult=1)
# With the correct mode no other bonds are made
assert not imag_mode_generates_other_bonds(
ts=calc.molecule,
f_species=f_species,
b_species=b_species,
bond_rearrangement=bond_rearrangement)
calc.output.filename = 'incorrect_ts_mode_g09.log'
calc.output.set_lines()
assert not imag_mode_has_correct_displacement(calc, bond_rearrangement)
os.chdir(here)
def test_edge_cases():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.6)
# For H3 with a slightly longer bond on one side there should only be 1 'bond'
h3 = Species(name='H2', atoms=[h_a, h_b, h_c], charge=0, mult=1)
mol_graphs.make_graph(h3)
assert h3.graph.number_of_edges() == 1
assert h3.graph.number_of_nodes() == 3
def test_ts_template():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.4)
ts_template = Species(name='template', charge=0, mult=1,
atoms=[h_a, h_b, h_c])
mol_graphs.make_graph(species=ts_template, allow_invalid_valancies=True)
ts_template.graph.edges[0, 1]['active'] = True
ts = Species(name='template', charge=0, mult=1, atoms=[h_a, h_b, h_c])
mol_graphs.make_graph(species=ts, allow_invalid_valancies=True)
ts.graph.edges[1, 2]['active'] = True
mapping = mol_graphs.get_mapping_ts_template(ts.graph, ts_template.graph)
assert mapping is not None
assert type(mapping) == dict
assert mol_graphs.is_isomorphic(ts.graph, ts_template.graph, ignore_active_bonds=True)
def test_species_solvent():
assert mol.solvent is None
solvated_mol = Species(name='H2',
atoms=[h1, h2],
charge=0,
mult=1,
solvent_name='water')
assert type(solvated_mol.solvent) == Solvent
def test_truncated_active_graph():
h_c = Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.4)
h_d = Atom(atomic_symbol='H', x=0.0, y=0.0, z=2.1)
ts = Species(name='template', charge=0, mult=1, atoms=[h_a, h_b, h_c, h_d])
mol_graphs.make_graph(species=ts, allow_invalid_valancies=True)
# H--active--H--H--H should truncate by keeping only the nearest neighbours to the first two atoms
truncated_graph = mol_graphs.get_truncated_active_mol_graph(ts.graph, active_bonds=[(0, 1)])
assert truncated_graph.number_of_nodes() == 3
assert truncated_graph.number_of_edges() == 2
def test_remove_bonds():
b3h6 = Species(name='diborane', charge=0, mult=1,
atoms=[Atom('B', -1.97106, 0.36170, -0.23984),
Atom('H', -0.91975, -0.06081, 0.43901),
Atom('H', -2.14001, -0.24547, -1.26544),
Atom('H', -2.99029, 0.31275, 0.39878),
Atom('B', -0.49819, 1.17500, 0.23984),
Atom('H', 0.52102, 1.22392, -0.39880),
Atom('H', -0.32919, 1.78217, 1.26543),
Atom('H', -1.54951, 1.59751, -0.43898)])
mol_graphs.make_graph(species=b3h6)
assert b3h6.graph.number_of_edges() == 6
assert b3h6.graph.number_of_nodes() == 8
# Boron atoms should be 3 fold valent
assert len(list(b3h6.graph.neighbors(0))) == 3
assert len(list(b3h6.graph.neighbors(4))) == 3
def imag_mode_has_correct_displacement(calc,
bond_rearrangement,
disp_mag=1.0,
delta_threshold=0.3,
req_all=True):
"""
Check whether the imaginary mode in a calculation with a hessian forms and
breaks the correct bonds
Arguments:
calc (autode.calculation.Calculation):
bond_rearrangement (autode.bond_rearrangement.BondRearrangement):
Keyword Arguments:
disp_mag (float):
delta_threshold (float): Required ∆r on a bond for the bond to be
considered as forming
req_all (bool): Require all the bonds to have the correct displacements
Returns:
(bool):
"""
logger.info('Checking displacement on imaginary mode forms the correct'
' bonds')
ts_species = deepcopy(calc.molecule)
f_displaced_atoms = get_displaced_atoms_along_mode(calc,
mode_number=6,
disp_magnitude=disp_mag)
f_species = Species(name='f_displaced',
atoms=f_displaced_atoms,
charge=0,
mult=1) # Charge & mult are placeholders
b_displaced_atoms = get_displaced_atoms_along_mode(
calc, mode_number=6, disp_magnitude=-disp_mag)
b_species = Species(name='b_displaced',
atoms=b_displaced_atoms,
charge=0,
mult=1)
if imag_mode_generates_other_bonds(ts_species, f_species, b_species,
bond_rearrangement):
logger.warning('Imaginary mode generates bonds that are not active..')
return False
# Product could be either the forward displaced molecule or the backwards
# equivalent
for product in (f_species, b_species):
fbond_bbond_correct_disps = []
for fbond in bond_rearrangement.fbonds:
ts_dist = ts_species.get_distance(*fbond)
p_dist = product.get_distance(*fbond)
# Displaced distance towards products should be shorter than the
# distance at the TS if the bond is forming
if ts_dist - p_dist > delta_threshold:
fbond_bbond_correct_disps.append(True)
else:
fbond_bbond_correct_disps.append(False)
for bbond in bond_rearrangement.bbonds:
ts_dist = ts_species.get_distance(*bbond)
p_dist = product.get_distance(*bbond)
# Displaced distance towards products should be longer than the
# distance at the TS if the bond is breaking
if p_dist - ts_dist > delta_threshold:
fbond_bbond_correct_disps.append(True)
else:
fbond_bbond_correct_disps.append(False)
logger.info(f'List of forming and breaking bonds that have the '
f'correct properties {fbond_bbond_correct_disps}')
if all(fbond_bbond_correct_disps) and req_all:
logger.info(f'{product.name} afforded the correct bond '
f'forming/breaking reactants -> products')
return True
if not req_all and any(fbond_bbond_correct_disps):
logger.info('At least one bond had the correct displacement')
return True
logger.warning('Displacement along the imaginary mode did not form and '
'break the correct bonds')
return False
from autode.wrappers.ORCA import orca
from autode.wrappers.XTB import xtb
from autode.atoms import Atom
from autode.solvent.solvents import Solvent
from autode.exceptions import NoAtomsInMolecule
from copy import deepcopy
import numpy as np
import pytest
import os
here = os.path.dirname(os.path.abspath(__file__))
h1 = Atom('H')
h2 = Atom('H', z=1.0)
mol = Species(name='H2', atoms=[h1, h2], charge=0, mult=1)
def test_species_class():
assert hasattr(mol, 'print_xyz_file')
assert hasattr(mol, 'translate')
assert hasattr(mol, 'rotate')
assert hasattr(mol, 'get_coordinates')
assert hasattr(mol, 'set_atoms')
assert hasattr(mol, 'set_coordinates')
assert mol.charge == 0
assert mol.mult == 1
assert mol.name == 'H2'
def test_isomorphic_graphs():
h2_alt = Species(name='H2', atoms=[h_b, h_a], charge=0, mult=1)
mol_graphs.make_graph(h2_alt)
assert mol_graphs.is_isomorphic(h2.graph, h2_alt.graph) is True
def test_set_lowest_energy_conformer():
from autode.mol_graphs import make_graph
hb = Atom('H', z=0.7)
hydrogen = Species(name='H2', atoms=[h1, hb], charge=0, mult=1)
make_graph(hydrogen)
hydrogen_wo_e = Species(name='H2', atoms=[h1, hb], charge=0, mult=1)
hydrogen_with_e = Species(name='H2', atoms=[h1, hb], charge=0, mult=1)
hydrogen_with_e.energy = -1
hydrogen.conformers = [hydrogen_wo_e, hydrogen_with_e]
hydrogen._set_lowest_energy_conformer()
# Conformers without energy should be skipped
assert hydrogen.energy == -1
# Conformers with a different molecular graph should be skipped
h_atom = Species(name='H', atoms=[Atom('H')], charge=0, mult=1)
h_atom.energy = -2
hydrogen.conformers = [hydrogen_with_e, h_atom]
assert hydrogen.energy == -1
from autode.pes.pes_2d import PES2d
from autode.pes.pes import get_closest_species
from autode.species.complex import ReactantComplex, ProductComplex
from autode.atoms import Atom
from autode.species.species import Species
from autode.mol_graphs import make_graph
from autode.exceptions import NoClosestSpecies
from autode.pes.pes import FormingBond, BreakingBond
from autode.reactions.reaction import Reaction
from autode.species.molecule import Reactant, Product
import pytest
import numpy as np
mol = Species(name='H2', charge=0, mult=1, atoms=[Atom(atomic_symbol='H', x=0.0, y=0.0, z=0.0),
Atom(atomic_symbol='H', x=0.0, y=0.0, z=1.0)])
make_graph(mol)
reactant = ReactantComplex(mol, mol)
product = ProductComplex(mol, mol)
pes = PES2d(reactant=reactant, product=reactant,
r1s=np.linspace(1, 3, 3), r1_idxs=(0, 1),
r2s=np.linspace(1, 0, 2), r2_idxs=(2, 3))
def test_2d_pes_class():
assert reactant.n_atoms == 4
assert pes.rs.shape == (3, 2)
assert pes.species.shape == (3, 2)
from autode.species.molecule import Molecule
from autode.atoms import Atom
from autode.conformers import Conformer
from autode.input_output import xyz_file_to_atoms
from . import testutils
import networkx as nx
import numpy as np
import pytest
import os
here = os.path.dirname(os.path.abspath(__file__))
h_a = Atom(atomic_symbol='H', x=0.0, y=0.0, z=0.0)
h_b = Atom(atomic_symbol='H', x=0.0, y=0.0, z=0.7)
h2 = Species(name='H2', atoms=[h_a, h_b], charge=0, mult=1)
mol_graphs.make_graph(h2)
g = nx.Graph()
edges = [(0, 1), (1, 2), (2, 0), (0, 3), (3, 4)]
for edge in edges:
g.add_edge(*edge)
def test_graph_generation():
assert h2.graph.number_of_edges() == 1
assert h2.graph.number_of_nodes() == 2
assert h2.graph.nodes[0]['atom_label'] == 'H'
from autode.species.complex import ReactantComplex
from autode.species.species import Species
from autode.atoms import Atom
from autode.substitution import SubstitutionCentre
from autode.mol_graphs import make_graph
from autode.substitution import attack_cost
from autode.substitution import get_cost_rotate_translate
import numpy as np
nh3 = Species(name='nh3', charge=0, mult=1, atoms=[Atom('N', -3.13130, 0.40668, -0.24910),
Atom('H', -3.53678, 0.88567, 0.55690),
Atom('H', -3.33721, 1.03222, -1.03052),
Atom('H', -3.75574, -0.38765, -0.40209)])
make_graph(nh3)
ch3cl = Species(name='CH3Cl', charge=0, mult=1, atoms=[Atom('Cl', 1.63751, -0.03204, -0.01858),
Atom('C', -0.14528, 0.00318, 0.00160),
Atom('H', -0.49672, -0.50478, 0.90708),
Atom('H', -0.51741, -0.51407, -0.89014),
Atom('H', -0.47810, 1.04781, 0.00015)])
make_graph(ch3cl)
def test_attack():
reactant = ReactantComplex(nh3, ch3cl)
subst_centre = SubstitutionCentre(a_atom_idx=0, c_atom_idx=5, x_atom_idx=4, a_atom_nn_idxs=[1, 2, 3])
subst_centre.r0_ac = 1.38
from autode.pes.pes_2d import PES2d
from autode.pes.pes import get_closest_species
from autode.species.complex import ReactantComplex, ProductComplex
from autode.atoms import Atom
from autode.species.species import Species
from autode.mol_graphs import make_graph
from autode.exceptions import NoClosestSpecies
from autode.pes.pes import FormingBond, BreakingBond
from autode.reactions.reaction import Reaction
from autode.species.molecule import Reactant, Product
import pytest
import numpy as np
mol = Species(name='H2', charge=0, mult=1, atoms=[Atom('H'), Atom('H', z=1.0)])
make_graph(mol)
reactant = ReactantComplex(mol, mol)
product = ProductComplex(mol, mol)
pes = PES2d(reactant=reactant,
product=reactant,
r1s=np.linspace(1, 3, 3),
r1_idxs=(0, 1),
r2s=np.linspace(1, 0, 2),
r2_idxs=(2, 3))
def test_2d_pes_class():
assert reactant.n_atoms == 4
assert pes.rs.shape == (3, 2)
def test_is_linear():
h_atom = Species(name='h', atoms=[Atom('H')], charge=0, mult=1)
assert not h_atom.is_linear()
dihydrogen = Species(name='h2',
atoms=[Atom('H'), Atom('H', x=1)],
charge=0,
mult=1)
assert dihydrogen.is_linear()
water = Species(name='water',
charge=0,
mult=1,
atoms=[
Atom('O', x=-1.52, y=2.72),
Atom('H', x=-0.54, y=2.72),
Atom('H', x=-1.82, y=2.82, z=-0.92)
])
assert not water.is_linear()
lin_water = Species(name='linear_water',
charge=0,
mult=1,
atoms=[
Atom('O', x=-1.52, y=2.72),
Atom('H', x=-1.21, y=2.51, z=1.03),
Atom('H', x=-1.82, y=2.82, z=-0.92)
])
assert lin_water.is_linear()
close_lin_water = Species(name='linear_water',
charge=0,
mult=1,
atoms=[
Atom('O', x=-1.52, y=2.72),
Atom('H', x=-0.90, y=2.36, z=0.89),
Atom('H', x=-1.82, y=2.82, z=-0.92)
])
assert not close_lin_water.is_linear()
acetylene = Molecule(smiles='C#C')
assert acetylene.is_linear()
