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A Practical Guide to the Design of Molecular Crystals
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Abstract This Tutorial Review, aimed at both the novice and the seasoned solid-state chemist, provides a succinct overview of key findings that have, over the last half century, advanced our ability to make molecular crystals with targeted structures and desired properties. The article critically evaluates the efficiency and reliability of the well-established guidelines used by experimentalists in crystal engineering and highlights statistical and computational tools that are both advantageous to crystal design and accessible to experimental solid-state chemists.
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Citations
Cites
van der Waals Volumes and Radii
Bondi, A. (1964) · The Journal of Physical Chemistry · doi:10.1021/j100785a001 · Cited by 19,350
Structure validation in chemical crystallography
Spek, A. L. (2009) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s090744490804362x · Cited by 15,432
The Cambridge Structural Database
Groom, C. R., Bruno, I. J., Lightfoot, M. P., & Ward, S. C. (2016) · Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials · doi:10.1107/s2052520616003954 · Cited by 10,297
Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals
Bernstein, J., Davis, R. E., Shimoni, L., & Chang, N. (1995) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199515551 · Cited by 8,228
Spackman, M. A., & Jayatilaka, D. (2009) · CrystEngComm · doi:10.1039/b818330a · Cited by 7,991
The Hydrogen Bond in the Solid State
Steiner, T. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020104)41:1<48::aid-anie48>3.0.co;2-u · Cited by 6,247
An introduction to hydrogen bonding
(1998) · Choice Reviews Online · doi:10.5860/choice.35-3309 · Cited by 6,199
Supramolecular Synthons in Crystal Engineering—A New Organic Synthesis
Desiraju, G. R. (1995) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199523111 · Cited by 4,856
Encoding and decoding hydrogen-bond patterns of organic compounds
Etter, M. C. (1990) · Accounts of Chemical Research · doi:10.1021/ar00172a005 · Cited by 4,591
Cavallo, G., Metrangolo, P., Milani, R., Pilati, T., Priimagi, A., Resnati, G., & Terraneo, G. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00484 · Cited by 4,035
Desiraju, G., & Steiner, T. (2001) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198509707.001.0001 · Cited by 3,791
New software for searching the Cambridge Structural Database and visualizing crystal structures
Bruno, I. J., Cole, J. C., Edgington, P. R., Kessler, M., Macrae, C. F., McCabe, P., Pearson, J., & Taylor, R. (2002) · Acta Crystallographica Section B Structural Science · doi:10.1107/s0108768102003324 · Cited by 3,126
Band alignment of rutile and anatase TiO2
Scanlon, D. O., Dunnill, C. W., Buckeridge, J., Shevlin, S. A., Logsdail, A. J., Woodley, S. M., Catlow, C. R. A., Powell, M. J., Palgrave, R. G., Parkin, I. P., et al. (2013) · Nature Materials · doi:10.1038/nmat3697 · Cited by 2,319
Clark, T., Hennemann, M., Murray, J. S., & Politzer, P. (2007) · Journal of Molecular Modeling · doi:10.1007/s00894-006-0130-2 · Cited by 2,314
Computational Methods in Drug Discovery
Sliwoski, G., Kothiwale, S., Meiler, J., & Lowe, E. W. (2014) · Pharmacological Reviews · doi:10.1124/pr.112.007336 · Cited by 2,160
Photodimerization in the solid state
Schmidt, G. M. J. (1971) · Pure and Applied Chemistry · doi:10.1351/pac197127040647 · Cited by 2,095
Hydrogen Bridges in Crystal Engineering: Interactions without Borders
Desiraju, G. R. (2002) · Accounts of Chemical Research · doi:10.1021/ar010054t · Cited by 2,057
Definition of the halogen bond (IUPAC Recommendations 2013).
Desiraju, G. R., Ho, P. S., Kloo, L., Legon, A. C., Marquardt, R., Metrangolo, P., Politzer, P., Resnati, G., & Rissanen, K. (2013) · Pure and Applied Chemistry · doi:10.1351/pac-rec-12-05-10 · Cited by 1,957
Halogen Bonding Based Recognition Processes: A World Parallel to Hydrogen Bonding
Metrangolo, P., Neukirch, H., Pilati, T., & Resnati, G. (2005) · Accounts of Chemical Research · doi:10.1021/ar0400995 · Cited by 1,915
Definition of the hydrogen bond (IUPAC Recommendations 2011)
Arunan, E., Desiraju, G. R., Klein, R. A., Sadlej, J., Scheiner, S., Alkorta, I., Clary, D. C., Crabtree, R. H., Dannenberg, J. J., Hobza, P., et al. (2011) · Pure and Applied Chemistry · doi:10.1351/pac-rec-10-01-02 · Cited by 1,886
The C−H···O Hydrogen Bond: Structural Implications and Supramolecular Design
Desiraju, G. R. (1996) · Accounts of Chemical Research · doi:10.1021/ar950135n · Cited by 1,870
Organic Optoelectronic Materials: Mechanisms and Applications
Ostroverkhova, O. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00127 · Cited by 1,680
Crystal Engineering: From Molecule to Crystal
Desiraju, G. R. (2013) · Journal of the American Chemical Society · doi:10.1021/ja403264c · Cited by 1,517
An analysis of the attrition of drug candidates from four major pharmaceutical companies
Waring, M. J., Arrowsmith, J., Leach, A. R., Leeson, P. D., Mandrell, S., Owen, R. M., Pairaudeau, G., Pennie, W. D., Pickett, S. D., Wang, J., et al. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd4609 · Cited by 1,450
Integrated Materials Design of Organic Semiconductors for Field-Effect Transistors
Mei, J., Diao, Y., Appleton, A. L., Fang, L., & Bao, Z. (2013) · Journal of the American Chemical Society · doi:10.1021/ja400881n · Cited by 1,443
Mackenzie, C. F., Spackman, P. R., Jayatilaka, D., & Spackman, M. A. (2017) · IUCrJ · doi:10.1107/s205225251700848x · Cited by 1,435
Polymorphism in Molecular Crystals
Bernstein, J. (2007) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199236565.001.0001 · Cited by 1,346
Halogen Bonding in Supramolecular Chemistry
Gilday, L. C., Robinson, S. W., Barendt, T. A., Langton, M. J., Mullaney, B. R., & Beer, P. D. (2015) · Chemical Reviews · doi:10.1021/cr500674c · Cited by 1,339
The C-H.cntdot..cntdot..cntdot.O hydrogen bond in crystals: what is it?
Desiraju, G. R. (1991) · Accounts of Chemical Research · doi:10.1021/ar00010a002 · Cited by 1,272
Organic chemical crystallography
Kitaǐgorodskiǐ, A. I. (1961) · Consultants Bureau eBooks · Cited by 1,127
The Cambridge Structural Database in Retrospect and Prospect
Groom, C. R., & Allen, F. H. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201306438 · Cited by 1,124
Quantifying Intermolecular Interactions: Guidelines for the Molecular Recognition Toolbox
Hunter, C. A. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200301739 · Cited by 1,097
Molecular crystals and molecules
(1974) · Materials Research Bulletin · doi:10.1016/0025-5408(74)90199-8 · Cited by 1,092
Khadka, P., Ro, J., Kim, H., Kim, I., Kim, J. T., Kim, H., Cho, J. M., Yun, G., & Lee, J. (2014) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2014.05.005 · Cited by 998
Retrieval of Crystallographically-Derived Molecular Geometry Information
Bruno, I. J., Cole, J. C., Kessler, M., Luo, J., Motherwell, W. D. S., Purkis, L. H., Smith, B. R., Taylor, R., Cooper, R. I., Harris, S. E., et al. (2004) · Journal of Chemical Information and Computer Sciences · doi:10.1021/ci049780b · Cited by 983
Pharmaceutical cocrystals: along the path to improved medicines
Duggirala, N. K., Perry, M. L., Almarsson, Ö., & Zaworotko, M. J. (2016) · Chemical Communications · doi:10.1039/c5cc08216a · Cited by 928
Structures of Complexes Formed by Halogen Molecules with Aromatic and with Oxygenated Solvents1
Mulliken, R. S. (1950) · Journal of the American Chemical Society · doi:10.1021/ja01157a151 · Cited by 923
Simard, M., Su, D., & Wuest, J. D. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00012a057 · Cited by 844
Dunitz, J. D., & Bernstein, J. (1995) · Accounts of Chemical Research · doi:10.1021/ar00052a005 · Cited by 843
The Nature of the Hydrogen Bond
Gilli, G., & Gilli, P. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199558964.001.0001 · Cited by 819
The Theory of Intermolecular Forces
Stone, A. (2013) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199672394.001.0001 · Cited by 817
The Nature and Geometry of Intermolecular Interactions between Halogens and Oxygen or Nitrogen
Lommerse, J. P. M., Stone, A. J., Taylor, R., & Allen, F. H. (1996) · Journal of the American Chemical Society · doi:10.1021/ja953281x · Cited by 806
Bernstein, J., Davey, R. J., & Henck, J. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19991203)38:23<3440::aid-anie3440>3.0.co;2-# · Cited by 774
Building co-crystals with molecular sense and supramolecular sensibility
Aakeröy, C. B., & Salmon, D. J. (2005) · CrystEngComm · doi:10.1039/b505883j · Cited by 770
Recent advances in crystal engineering
Aakeröy, C. B., Champness, N. R., & Janiak, C. (2010) · CrystEngComm · doi:10.1039/b919819a · Cited by 746
C−H···F Interactions in the Crystal Structures of Some Fluorobenzenes
Thalladi, V. R., Weiss, H.-C., Bläser, D., Boese, R., Nangia, A., & Desiraju, G. R. (1998) · Journal of the American Chemical Society · doi:10.1021/ja981198e · Cited by 731
Molecular packing modes. Carboxylic acids
Leiserowitz, L. (1976) · Acta Crystallographica Section B · doi:10.1107/s0567740876003968 · Cited by 702
Facts and fictions about polymorphism
Cruz-Cabeza, A. J., Reutzel-Edens, S. M., & Bernstein, J. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00227c · Cited by 678
Acid–base crystalline complexes and the pKa rule
Cruz-Cabeza, A. J. (2012) · CrystEngComm · doi:10.1039/c2ce26055g · Cited by 673
Gavezzotti, A. (1983) · Journal of the American Chemical Society · doi:10.1021/ja00354a007 · Cited by 595
Crystal structures of drugs: advances in determination, prediction and engineering
Datta, S., & Grant, D. J. W. (2004) · Nature Reviews Drug Discovery · doi:10.1038/nrd1280 · Cited by 583
Desiraju, G. R. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201002960 · Cited by 575
Turner, M. J., Grabowsky, S., Jayatilaka, D., & Spackman, M. A. (2014) · The Journal of Physical Chemistry Letters · doi:10.1021/jz502271c · Cited by 549
Modular and predictable assembly of porous organic molecular crystals
Jones, J. T. A., Hasell, T., Wu, X., Bacsa, J., Jelfs, K. E., Schmidtmann, M., Chong, S. Y., Adams, D. J., Trewin, A., Schiffman, F., et al. (2011) · Nature · doi:10.1038/nature10125 · Cited by 521
Hydrogen bond-directed cocrystallization and molecular recognition properties of diarylureas
Etter, M. C., Urbanczyk-Lipkowska, Z., Zia-Ebrahimi, M., & Panunto, T. W. (1990) · Journal of the American Chemical Society · doi:10.1021/ja00179a028 · Cited by 507
Functional materials discovery using energy–structure–function maps
Pulido, A., Chen, L., Kaczorowski, T., Holden, D., Little, M. A., Chong, S. Y., Slater, B. J., McMahon, D. P., Bonillo, B., Stackhouse, C. J., et al. (2017) · Nature · doi:10.1038/nature21419 · Cited by 506
Crystal Engineering: A Textbook
Desiraju, G. R., Vittal, J. J., & Ramanan, A. (2011) · Co-Published with Indian Institute of Science (IISc), Bangalore, India eBooks · doi:10.1142/8060 · Cited by 498
Structural Aspects of Interatomic Charge-Transfer Bonding
Hassel, O. (1970) · Science · doi:10.1126/science.170.3957.497 · Cited by 470
Organic Donor–Acceptor Complexes as Novel Organic Semiconductors
Zhang, J., Xu, W., Sheng, P., Zhao, G., & Zhu, D. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00124 · Cited by 441
Dunitz, J. D. (2004) · ChemBioChem · doi:10.1002/cbic.200300801 · Cited by 423
Some aspects of organic pigments
Hao, Z.-M., & Iqbal, A. F. M. (1997) · Chemical Society Reviews · doi:10.1039/cs9972600203 · Cited by 407
Disappearing Polymorphs Revisited
Bučar, D., Lancaster, R. W., & Bernstein, J. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201410356 · Cited by 395
Self-citationStructural Competition between Hydrogen Bonds and Halogen Bonds
Aakeröy, C. B., Fasulo, M., Schultheiss, N., Desper, J., & Moore, C. (2007) · Journal of the American Chemical Society · doi:10.1021/ja073201c · Cited by 394
Bui, T. T. T., Dahaoui, S., Lecomte, C., Desiraju, G. R., & Espinosa, E. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200805739 · Cited by 378
Crystal engineering, Where from? Where to?
Braga, D. (2003) · Chemical Communications · doi:10.1039/b306269b · Cited by 371
Sokolov, A. N., Atahan-Evrenk, S., Mondal, R., Akkerman, H. B., Sánchez-Carrera, R. S., Granados-Focil, S., Schrier, J., Mannsfeld, S. C. B., Zoombelt, A. P., Bao, Z., et al. (2011) · Nature Communications · doi:10.1038/ncomms1451 · Cited by 356
Role of organic fluorine in crystal engineering
Chopra, D., & Row, T. N. G. (2011) · CrystEngComm · doi:10.1039/c0ce00538j · Cited by 335
IsoStar: A library of information about nonbonded interactions
Bruno, I. J., Cole, J. C., Lommerse, J. P. M., Rowland, R. S., Taylor, R., & Verdonk, M. L. (1997) · Journal of Computer-Aided Molecular Design · doi:10.1023/a:1007934413448 · Cited by 325
De novo design of structure-directing agents for the synthesis of microporous solids
Lewis, D. W., Willock, D. J., Catlow, C. R. A., Thomas, J. M., & Hutchings, G. J. (1996) · Nature · doi:10.1038/382604a0 · Cited by 312
The Prediction, Morphology, and Mechanical Properties of the Polymorphs of Paracetamol
Beyer, T., Day, G. M., & Price, S. L. (2001) · Journal of the American Chemical Society · doi:10.1021/ja0102787 · Cited by 302
How molecules stick together in organic crystals: weak intermolecular interactions
Dunitz, J. D., & Gavezzotti, A. (2009) · Chemical Society Reviews · doi:10.1039/b822963p · Cited by 301
The C–H… O Hydrogen Bond in Crystals
JUNE SUTOR, D. (1962) · Nature · doi:10.1038/195068a0 · Cited by 283
Cinčić, D., Friščić, T., & Jones, W. (2008) · Chemistry – A European Journal · doi:10.1002/chem.200701184 · Cited by 261
Fournier, J., Maris, T., Wuest, J. D., Guo, W., & Galoppini, E. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0276772 · Cited by 253
Clarke, H. D., Arora, K. K., Bass, H., Kavuru, P., Ong, T. T., Pujari, T., Wojtas, L., & Zaworotko, M. J. (2010) · Crystal Growth & Design · doi:10.1021/cg901345u · Cited by 248
Current approaches to predicting molecular organic crystal structures
Day, G. M. (2011) · Crystallography Reviews · doi:10.1080/0889311x.2010.517526 · Cited by 236
Why don't we find more polymorphs?
Price, S. L. (2013) · Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials · doi:10.1107/s2052519213018861 · Cited by 231
Hydrogen bonding vs. halogen bonding: the solvent decides
Robertson, C. C., Wright, J. S., Carrington, E. J., Perutz, R. N., Hunter, C. A., & Brammer, L. (2017) · Chemical Science · doi:10.1039/c7sc01801k · Cited by 222
Efficient Co-crystal Screening Using Solution-Mediated Phase Transformation
Zhang, G. G. Z., Henry, R. F., Borchardt, T. B., & Lou, X. (2007) · Journal of Pharmaceutical Sciences · doi:10.1002/jps.20949 · Cited by 217
Making crystals from crystals: a green route to crystal engineering and polymorphism
Braga, D., & Grepioni, F. (2005) · Chemical Communications · doi:10.1039/b504668h · Cited by 211
The Nature of the Intermolecular Forces Operative in Biological Processes
Pauling, L., & Delbrück, M. (1940) · Science · doi:10.1126/science.92.2378.77 · Cited by 211
Evaluating the Energetic Driving Force for Cocrystal Formation
Taylor, C. R., & Day, G. M. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.7b01375 · Cited by 206
Halogen bonds in some dihalogenated phenols: applications to crystal engineering
Mukherjee, A., & Desiraju, G. R. (2014) · IUCrJ · doi:10.1107/s2052252513025657 · Cited by 204
Type II halogen···halogen contacts are halogen bonds
Metrangolo, P., & Resnati, G. (2014) · IUCrJ · doi:10.1107/s205225251303491x · Cited by 189
Maschio, L., Civalleri, B., Ugliengo, P., & Gavezzotti, A. (2011) · The Journal of Physical Chemistry A · doi:10.1021/jp203132k · Cited by 179
Reflections on the Hydrogen Bond in Crystal Engineering
Desiraju, G. R. (2011) · Crystal Growth & Design · doi:10.1021/cg200100m · Cited by 173
Knowledge-based model of hydrogen-bonding propensity in organic crystals
Galek, P. T. A., Fábián, L., Motherwell, W. D. S., Allen, F. H., & Feeder, N. (2007) · Acta Crystallographica Section B Structural Science · doi:10.1107/s0108768107030996 · Cited by 170
Research applications of the Cambridge Structural Database (CSD)
Allen, F. H., & Taylor, R. (2004) · Chemical Society Reviews · doi:10.1039/b309040j · Cited by 166
On the inclusion of solvent molecules in the crystal structures of organic compounds
Görbitz, C. H., & Hersleth, H.-P. (2000) · Acta Crystallographica Section B Structural Science · doi:10.1107/s0108768100000501 · Cited by 128
Space-group frequencies for organic compounds
Mighell, A. D., Himes, V. L., & Rodgers, J. R. (1983) · Acta Crystallographica Section A Foundations of Crystallography · doi:10.1107/s0108767383001464 · Cited by 124
A rough guide to molecular solid solutions: design, synthesis and characterization of mixed crystals
Lusi, M. (2018) · CrystEngComm · doi:10.1039/c8ce00691a · Cited by 122
It Isn’t, It Is: The C–H···X (X = O, N, F, Cl) Interaction Really Is Significant in Crystal Packing
Taylor, R. (2016) · Crystal Growth & Design · doi:10.1021/acs.cgd.6b00736 · Cited by 108
Predicted energy–structure–function maps for the evaluation of small molecule organic semiconductors
Campbell, J. E., Yang, J., & Day, G. M. (2017) · Journal of Materials Chemistry C · doi:10.1039/c7tc02553j · Cited by 107
Lemmerer, A., Adsmond, D. A., Esterhuysen, C., & Bernstein, J. (2013) · Crystal Growth & Design · doi:10.1021/cg4006357 · Cited by 104
DDT Polymorphism and the Lethality of Crystal Forms
Yang, J., Hu, C., Zhu, X., et al. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201703028 · Cited by 97
Stilinović, V., Horvat, G., Hrenar, T., Nemec, V., & Cinčić, D. (2017) · Chemistry - A European Journal · doi:10.1002/chem.201605686 · Cited by 91
New solid forms of artemisinin obtained through cocrystallisation
Karki, S. B., Friščić, T., Fábián, L., & Jones, W. (2010) · CrystEngComm · doi:10.1039/c0ce00428f · Cited by 85
A cocrystallisation-based strategy to construct isostructural solids
Cinčić, D., Friščić, T., & Jones, W. (2008) · New Journal of Chemistry · doi:10.1039/b805816d · Cited by 83
Crystal Engineering with Iodoethynylnitrobenzenes: A Group of Highly Effective Halogen-Bond Donors
Aakeröy, C. B., Wijethunga, T. K., Desper, J. A., & Đaković, M. (2015) · Crystal Growth & Design · doi:10.1021/acs.cgd.5b00478 · Cited by 82
Honer, K., Kalfaoglu, E., Pico, C., McCann, J., & Baltrušaitis, J. (2017) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.7b02621 · Cited by 82
Kapadia, P. P., Ditzler, L. R., Baltrušaitis, J., Swenson, D. C., Tivanski, A. V., & Pigge, F. C. (2011) · Journal of the American Chemical Society · doi:10.1021/ja203001z · Cited by 81
Bučar, D., Sen, A., Mariappan, S. V. S., & MacGillivray, L. R. (2012) · Chemical Communications · doi:10.1039/c2cc15453f · Cited by 71
Self-citationSharma, C. V. K., Panneerselvam, K., Pilati, T., & Desiraju, G. R. (1993) · Journal of the Chemical Society Perkin Transactions 2 · doi:10.1039/p29930002209 · Cited by 69
The hydrogen bond between N—H or O—H and organic fluorine: favourable yes, competitive no
Taylor, R. (2017) · Acta Crystallographica Section B Structural Science Crystal Engineering and Materials · doi:10.1107/s2052520617005923 · Cited by 68
Towards an understanding of the propensity for crystalline hydrate formation by molecular compounds
Bajpai, A., Scott, H. S., Pham, T., Chen, K., Space, B., Lusi, M., Perry, M. L., & Zaworotko, M. J. (2016) · IUCrJ · doi:10.1107/s2052252516015633 · Cited by 67
Prediction of Hydrate and Solvate Formation Using Statistical Models
Takieddin, K., Khimyak, Y. Z., & Fábián, L. (2015) · Crystal Growth & Design · doi:10.1021/acs.cgd.5b00966 · Cited by 65
Corpinot, M. K., Stratford, S. A., Arhangelskis, M., Anka-Lufford, J., Halász, I., Judaš, N., Jones, W., & Bučar, D. (2016) · CrystEngComm · doi:10.1039/c6ce00293e · Cited by 60
Self-citationOrganic alloys of room temperature liquids thiophenol and selenophenol
Thomas, S. P., Sathishkumar, R., & Row, T. N. G. (2015) · Chemical Communications · doi:10.1039/c5cc03322e · Cited by 53
Organic crystal engineering beyond the Pauling hydrogen bond
Bishop, R. (2015) · CrystEngComm · doi:10.1039/c5ce01069a · Cited by 43
Are Oxygen and Sulfur Atoms Structurally Equivalent in Organic Crystals?
Corpinot, M. K., Guo, R., Tocher, D. A., Buanz, A. B. M., Gaisford, S., Price, S. L., & Bučar, D. (2016) · Crystal Growth & Design · doi:10.1021/acs.cgd.6b01669 · Cited by 42
Self-citationZbačnik, M., Pajski, M., Stilinović, V., Vitković, M., & Cinčić, D. (2017) · CrystEngComm · doi:10.1039/c7ce01332a · Cited by 39
GENERAL METHODS FOR THE CONSTRUCTION OF COMPLEX MOLECULES
Corey, E. J. (1967) · Elsevier eBooks · doi:10.1016/b978-0-08-020741-4.50004-x · Cited by 34
Engineering Molecular Crystals: Backbreaking, yet Gratifying
Bučar, D. (2017) · Crystal Growth & Design · doi:10.1021/acs.cgd.7b00210 · Cited by 30
Self-citationNowacki, W. (1943) · Helvetica Chimica Acta · doi:10.1002/hlca.19430260210 · Cited by 17
A quantitative measure of halogen bond activation in cocrystallization
Carlucci, L., & Gavezzotti, A. (2017) · Physical Chemistry Chemical Physics · doi:10.1039/c7cp03322b · Cited by 17
Cited by
Peluso, P., & Chankvetadze, B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00846 · Cited by 371
Metadata
- Authors
- Corpinot, M. K., & Bučar, D.-K.
- Venue
- Crystal Growth & Design
- Publisher
- American Chemical Society (ACS)
- Published
- 2018-12-06
- Volume
- 19
- Issue
- 2
- Pages
- 1426-1453
- ISSN
- 1528-7483 (ISSN-L)
- 1528-7505
- OpenAlex
- W2905015104
- Cited by
- 348
- References
- 116
- FWCI
- 23.47
- Type
- journal article
- Language
- en
- Open access
- hybrid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.