Crystallography Open Database for SOLSA

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Searching year of publication is 2016

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1529430 C36 H41 Na O6P 1 21/c 118.646; 12.596; 14.6475
90; 112.453; 90
3179.4Dai, Zhongran; Sun, Yangyang; Xiong, Jiao; Pan, Xiaobo; Tang, Ning; Wu, Jincai
Simple sodium and potassium phenolates as catalysts for highly isoselective polymerization of rac-lactide
Catal. Sci. Technol., 2016, 6, 515
1531039 C70.45 H104.45 Cl13.38 N8 O12.05P 114.3767; 24.3477; 24.5528
90.131; 93.427; 91.09
8577.5Rodríguez-Vázquez, Nuria; García-Fandiño, Rebeca; Amorín, Manuel; Granja, Juan R.
Self-assembling α,γ-cyclic peptides that generate cavities with tunable properties
Chem. Sci., 2016, 7, 183
1532462 C16 H22 N2 OP 1 21/n 114.4834; 6.1063; 16.8547
90; 104.786; 90
1441.27Khalil, Khaled D.; Ibrahim, Enas I.; Al-Sagheer, Fakhreia A.
A novel, efficient, and recyclable biocatalyst for Michael addition reactions and its iron(iii) complex as promoter for alkyl oxidation reactions
Catal. Sci. Technol., 2016, 6, 1410
1532463 C15 H20 N2 O2P 1 21/n 114.476; 6.097; 16.8438
90; 104.788; 90
1437.39Khalil, Khaled D.; Ibrahim, Enas I.; Al-Sagheer, Fakhreia A.
A novel, efficient, and recyclable biocatalyst for Michael addition reactions and its iron(iii) complex as promoter for alkyl oxidation reactions
Catal. Sci. Technol., 2016, 6, 1410
1532464 C11 H10 Co N O4P 6/m m m21.5645; 21.5645; 9.4379
90; 90; 120
3800.9Tu, Thach N.; Nguyen, Khoa D.; Nguyen, Truong N.; Truong, Thanh; Phan, Nam T. S.
New topological Co2(BDC)2(DABCO) as a highly active heterogeneous catalyst for the amination of oxazoles via oxidative C‒H/N‒H couplings
Catal. Sci. Technol., 2016, 6, 1384
1532467 C11 H7 F2 N3 O3 SC 1 2 126.261; 5.162; 9.7804
90; 111.188; 90
1236.2Zhang, Huatang; Liu, Ruochuan; Liu, Jie; Li, Lin; Wang, Ping; Yao, Shao Q.; Xu, Zhengtao; Sun, Hongyan
A minimalist fluorescent probe for differentiating Cys, Hcy and GSH in live cells
Chem. Sci., 2016, 7, 256
1532488 C15 H10 Br N3 O2P -15.2396; 10.766; 12.305
97.556; 93.106; 95.573
683.3Vincent-Rocan, Jean-François; Ivanovich, Ryan A.; Clavette, Christian; Leckett, Kyle; Bejjani, Julien; Beauchemin, André M.
Cascade reactions of nitrogen-substituted isocyanates: a new tool in heterocyclic chemistry
Chem. Sci., 2016, 7, 315
1532489 C18 H15 N3 SP 1 21/c 19.3536; 17.701; 9.8752
90; 111.505; 90
1521.2Vincent-Rocan, Jean-François; Ivanovich, Ryan A.; Clavette, Christian; Leckett, Kyle; Bejjani, Julien; Beauchemin, André M.
Cascade reactions of nitrogen-substituted isocyanates: a new tool in heterocyclic chemistry
Chem. Sci., 2016, 7, 315
1532503 C38 H80 Fe2 O6 P2 Si8P 1 21/c 115.6926; 17.5019; 21.2042
90; 110.633; 90
5450.2Sunada, Yusuke; Ishida, Shintaro; Hirakawa, Fumiya; Shiota, Yoshihito; Yoshizawa, Kazunari; Kanegawa, Shinji; Sato, Osamu; Nagashima, Hideo; Iwamoto, Takeaki
Persistent four-coordinate iron-centered radical stabilized by π-donation
Chem. Sci., 2016, 7, 191
1532504 C26 H52 Fe N O3 P Si4P -19.4542; 11.3877; 16.3807
75.408; 87.846; 79.154
1676.1Sunada, Yusuke; Ishida, Shintaro; Hirakawa, Fumiya; Shiota, Yoshihito; Yoshizawa, Kazunari; Kanegawa, Shinji; Sato, Osamu; Nagashima, Hideo; Iwamoto, Takeaki
Persistent four-coordinate iron-centered radical stabilized by π-donation
Chem. Sci., 2016, 7, 191
1532505 C22 H49 Fe O3 P Si5P -111.1846; 11.2283; 14.972
83.758; 76.946; 60.902
1600.5Sunada, Yusuke; Ishida, Shintaro; Hirakawa, Fumiya; Shiota, Yoshihito; Yoshizawa, Kazunari; Kanegawa, Shinji; Sato, Osamu; Nagashima, Hideo; Iwamoto, Takeaki
Persistent four-coordinate iron-centered radical stabilized by π-donation
Chem. Sci., 2016, 7, 191
1532506 C37 H56 Fe O3 P Si4 SnP 21 21 2111.387; 14.883; 24.983
90; 90; 90
4233.9Sunada, Yusuke; Ishida, Shintaro; Hirakawa, Fumiya; Shiota, Yoshihito; Yoshizawa, Kazunari; Kanegawa, Shinji; Sato, Osamu; Nagashima, Hideo; Iwamoto, Takeaki
Persistent four-coordinate iron-centered radical stabilized by π-donation
Chem. Sci., 2016, 7, 191
1534126 C16 H13 N O3P b c a7.2317; 11.2958; 32.232
90; 90; 90
2633Huang, Zheng; Askari, Mohammad S.; Esguerra, Kenneth Virgel N.; Dai, Tian-Yang; Kwon, Ohhyeon; Ottenwaelder, Xavier; Lumb, Jean-Philip
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C‒H functionalization of phenols
Chem. Sci., 2016, 7, 358
1534127 C17 H15 N O3P 1 21/c 15.792; 23.556; 11.041
90; 113.83; 90
1378Huang, Zheng; Askari, Mohammad S.; Esguerra, Kenneth Virgel N.; Dai, Tian-Yang; Kwon, Ohhyeon; Ottenwaelder, Xavier; Lumb, Jean-Philip
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C‒H functionalization of phenols
Chem. Sci., 2016, 7, 358
1534128 C18 H19 N O5P 1 21 111.1595; 6.7253; 11.4275
90; 103.413; 90
834.25Huang, Zheng; Askari, Mohammad S.; Esguerra, Kenneth Virgel N.; Dai, Tian-Yang; Kwon, Ohhyeon; Ottenwaelder, Xavier; Lumb, Jean-Philip
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C‒H functionalization of phenols
Chem. Sci., 2016, 7, 358
1534129 C23 H19 N O4P 21 21 217.6287; 11.5801; 20.615
90; 90; 90
1821.2Huang, Zheng; Askari, Mohammad S.; Esguerra, Kenneth Virgel N.; Dai, Tian-Yang; Kwon, Ohhyeon; Ottenwaelder, Xavier; Lumb, Jean-Philip
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C‒H functionalization of phenols
Chem. Sci., 2016, 7, 358
1534130 C54.5 H79 Cl5 Cu2 F12 N6 O6 Sb2P -113.668; 15.095; 19.109
79.735; 89.183; 63.926
3475Huang, Zheng; Askari, Mohammad S.; Esguerra, Kenneth Virgel N.; Dai, Tian-Yang; Kwon, Ohhyeon; Ottenwaelder, Xavier; Lumb, Jean-Philip
A bio-inspired synthesis of oxindoles by catalytic aerobic dual C‒H functionalization of phenols
Chem. Sci., 2016, 7, 358
1534131 C64 H54 B2 O4P -17.553; 12.357; 12.549
83.18; 74.39; 84.51
1117.6Osumi, Shinichiro; Saito, Shohei; Dou, Chuandong; Matsuo, Kyohei; Kume, Keita; Yoshikawa, Hirofumi; Awaga, Kunio; Yamaguchi, Shigehiro
Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance
Chem. Sci., 2016, 7, 219
1534132 C96 H118 B2 O4P -111.769; 14.134; 23.62
84.13; 87.54; 84.78
3890Osumi, Shinichiro; Saito, Shohei; Dou, Chuandong; Matsuo, Kyohei; Kume, Keita; Yoshikawa, Hirofumi; Awaga, Kunio; Yamaguchi, Shigehiro
Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance
Chem. Sci., 2016, 7, 219
1534133 C102 H130 B2 K3 N6 O18P 1 21/n 115.4324; 29.3994; 21.2075
90; 97.632; 90
9536.7Osumi, Shinichiro; Saito, Shohei; Dou, Chuandong; Matsuo, Kyohei; Kume, Keita; Yoshikawa, Hirofumi; Awaga, Kunio; Yamaguchi, Shigehiro
Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance
Chem. Sci., 2016, 7, 219

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