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Pillars of crystal engineering: crystal energies and symmetry operators
Pillars of crystal engineering: crystal energies and symmetry operators
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Pillars of crystal engineering: crystal energies and symmetry operators

Gavezzotti, A.

CrystEngComm, 2018, Vol.20 (18), p.2511-2518 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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Pillars of crystal engineering: crystal energies and symmetry operatorsElectronic supplementary information (ESI) available: Full tables of structure identifiers and details of the derivations. See DOI: 10.1039/c8ce00274f
Pillars of crystal engineering: crystal energies and symmetry operatorsElectronic supplementary information (ESI) available: Full tables of structure identifiers and details of the derivations. See DOI: 10.1039/c8ce00274f
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Pillars of crystal engineering: crystal energies and symmetry operatorsElectronic supplementary information (ESI) available: Full tables of structure identifiers and details of the derivations. See DOI: 10.1039/c8ce00274f

Gavezzotti, A

2018-05

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3
Self-organization of small organic molecules in liquids, solutions and crystals: static and dynamic calculations
Self-organization of small organic molecules in liquids, solutions and crystals: static and dynamic calculations
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Self-organization of small organic molecules in liquids, solutions and crystals: static and dynamic calculations

Gavezzotti, A. ; Filippini, G.

Chemical communications (Cambridge, England), 1998-02 (3), p.287-294 [Periódico revisado por pares]

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4
From molecular to crystal structure; polynuclear aromatic hydrocarbons
From molecular to crystal structure; polynuclear aromatic hydrocarbons
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From molecular to crystal structure; polynuclear aromatic hydrocarbons

DESIRAJU, G. R ; GAVEZZOTTI, A

Journal of the Chemical Society. Chemical communications, 1989 (10), p.621-623

Cambridge: Royal Society of Chemistry

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5
Molecular structure of p-nitrobiphenyl. A comparison of the results of X-ray crystal analysis with semi-empirical calculations of conformation
Molecular structure of p-nitrobiphenyl. A comparison of the results of X-ray crystal analysis with semi-empirical calculations of conformation
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Molecular structure of p-nitrobiphenyl. A comparison of the results of X-ray crystal analysis with semi-empirical calculations of conformation

Casalone, G. ; Gavezzotti, A. ; Simonetta, M.

Journal of the Chemical Society, Perkin Transactions 2, 1973 (4), p.342 [Periódico revisado por pares]

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6
Crystal and molecular structure of 1,6:8,13-propane-1,3-diylidene[14]-annulene
Crystal and molecular structure of 1,6:8,13-propane-1,3-diylidene[14]-annulene
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Crystal and molecular structure of 1,6:8,13-propane-1,3-diylidene[14]-annulene

Gavezzotti, A. ; Mugnoli, A. ; Raimondi, M. ; Simonetta, M.

Journal of the Chemical Society, Perkin Transactions 2, 1972 (4), p.425 [Periódico revisado por pares]

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MOLECULAR-ORGANIZATION IN CRYSTALLINE [CO2(CO)8] AND [FE2(CO)9] AND A SEARCH FOR ALTERNATIVE PACKINGS FOR [CO2(CO)8]
MOLECULAR-ORGANIZATION IN CRYSTALLINE [CO2(CO)8] AND [FE2(CO)9] AND A SEARCH FOR ALTERNATIVE PACKINGS FOR [CO2(CO)8]
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MOLECULAR-ORGANIZATION IN CRYSTALLINE [CO2(CO)8] AND [FE2(CO)9] AND A SEARCH FOR ALTERNATIVE PACKINGS FOR [CO2(CO)8]

BRAGA, D ; GREPIONI, F ; SABATINO, P ; GAVEZZOTTI, A

Journal of the Chemical Society. Dalton transactions, 1992 (7), p.1185-1191

CAMBRIDGE: Royal Soc Chemistry

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8
Efficient computer modeling of organic materials. The atom–atom, Coulomb–London–Pauli (AA-CLP) model for intermolecular electrostatic-polarization, dispersion and repulsion energies
Efficient computer modeling of organic materials. The atom–atom, Coulomb–London–Pauli (AA-CLP) model for intermolecular electrostatic-polarization, dispersion and repulsion energies
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Efficient computer modeling of organic materials. The atom–atom, Coulomb–London–Pauli (AA-CLP) model for intermolecular electrostatic-polarization, dispersion and repulsion energies

Gavezzotti, Angelo

New journal of chemistry, 2011, Vol.35 (7), p.1360 [Periódico revisado por pares]

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9
Comparing the strength of covalent bonds, intermolecular hydrogen bonds and other intermolecular interactions for organic molecules: X-ray diffraction data and quantum chemical calculations
Comparing the strength of covalent bonds, intermolecular hydrogen bonds and other intermolecular interactions for organic molecules: X-ray diffraction data and quantum chemical calculations
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Comparing the strength of covalent bonds, intermolecular hydrogen bonds and other intermolecular interactions for organic molecules: X-ray diffraction data and quantum chemical calculations

Gavezzotti, Angelo

New journal of chemistry, 2016, Vol.40 (8), p.6848-6853 [Periódico revisado por pares]

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10
Book reviews
Book reviews
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Book reviews

Barron, A. R. ; Flavell, W. ; Gavezzotti, A. ; Plater, M. J.

Journal of Materials Chemistry, 1995, Vol.5 (5), p.801 [Periódico revisado por pares]

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