Crystallography Open Database

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1556908 CIFC20 H23 N3 O3P 21 21 217.191; 13.5045; 18.6644
90; 90; 90
1812.52Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556909 CIFC20 H25 N3 O2P 1 21/n 16.8118; 17.5495; 15.1113
90; 91.427; 90
1805.9Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556910 CIFC22 H21.25 N3 O2.125P 1 21 110.18405; 9.71457; 18.82762
90; 93.0169; 90
1860.1Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556911 CIFC24 H21 F3 N2 O4 SP 21 21 2132.8358; 11.60538; 5.85758
90; 90; 90
2232.16Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556912 CIFC22 H25 N3 O2P 1 21 112.4713; 9.02632; 17.84198
90; 92.8702; 90
2005.95Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556913 CIFC20 H19 N3 OP 1 21 110.10659; 5.94958; 13.62038
90; 99.5974; 90
807.53Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556914 CIFC28 H30 N2 O2P 21 21 218.33247; 15.71709; 17.93381
90; 90; 90
2348.65Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556915 CIFC24 H24 N2 O4 SP 21 21 216.0985; 11.5023; 30.8387
90; 90; 90
2163.2Dean, Conor; Rajkumar, Sundaram; Roesner, Stefan; Carson, Nessa; Clarkson, Guy J.; Wills, Martin; Jones, Matthew; Shipman, Michael
Readily accessible sp<sup>3</sup>-rich cyclic hydrazine frameworks exploiting nitrogen fluxionality.
Chemical science, 2020, 11, 1636-1642
1556927 CIFC9 H19 I2 N3 PdC 1 2/c 114.7908; 7.8079; 27.592
90; 99.197; 90
3145.5Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556928 CIFC13 H21 I2 N3 PdP 1 21/c 117.5721; 12.5994; 8.4655
90; 99.55; 90
1848.27Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556929 CIFC15 H17 I2 N3 PdC 1 2/c 121.6545; 8.657; 20.1671
90; 95.408; 90
3763.8Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556930 CIFC16 H19 I2 N3 PdP -19.5333; 10.964; 11.3716
62.48; 79.571; 67.896
976.59Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556981 CIFLa3 Li6.5 Nb0.5 O12 Zr1.5I a -3 d12.913; 12.913; 12.913
90; 90; 90
2153.2Kataoka, K.
Oxide single crystals with high lithium-ion conductivity as solid electrolytes for all-solid-state lithium secondary battery applications
Journal of the Ceramic Society of Japan, 2020, 128, 7-18
1556982 CIFLa3 Li6.5 O12 Ta0.5 Zr1.5I a -3 d12.9445; 12.9445; 12.9445
90; 90; 90
2168.98Kataoka, K.
Oxide single crystals with high lithium-ion conductivity as solid electrolytes for all-solid-state lithium secondary battery applications
Journal of the Ceramic Society of Japan, 2020, 128, 7-18
1556983 CIFC23 H19.35 N5 O4.18P 21 21 217.4338; 19.1874; 28.7281
90; 90; 90
4097.64Lin, Shuang; Yu, Huimin; Yang, Beiye; Li, Fengli; Chen, Xia; Li, Huaqiang; Zhang, Sitian; Wang, Jianping; Hu, Youcai; Hu, Zhengxi; Zhang, Yonghui
Reisolation and Configurational Reinvestigation of Cottoquinazolines E-G from an Arthropod-Derived Strain of the Fungus <i>Neosartorya fischeri</i>.
Journal of natural products, 2020, 83, 169-173
1556984 CIFC25 H25 N5 O5P 6113.718; 13.718; 21.48
90; 90; 120
3500.6Lin, Shuang; Yu, Huimin; Yang, Beiye; Li, Fengli; Chen, Xia; Li, Huaqiang; Zhang, Sitian; Wang, Jianping; Hu, Youcai; Hu, Zhengxi; Zhang, Yonghui
Reisolation and Configurational Reinvestigation of Cottoquinazolines E-G from an Arthropod-Derived Strain of the Fungus <i>Neosartorya fischeri</i>.
Journal of natural products, 2020, 83, 169-173
1556985 CIFC6 H12 N4 O8 P2 S2P 1 21/c 14.6777; 8.716; 17.1651
90; 91.394; 90
699.628Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556986 CIFC6 H20 N4 O16 P4 S2P 1 21/n 111.0254; 7.0847; 13.0691
90; 96.516; 90
1014.26Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556987 CIFC3 H6 N2 O4 P SP -15.40917; 7.805; 8.856
63.995; 84.123; 83.101
333.08Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556988 CIFC3 H9 N2 O8 P2 SP -15.26221; 8.96277; 10.8217
97.609; 95.9417; 98.5964
496.242Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556989 CIFC6 H9 N4 O4 P S2P 1 21/c 113.8433; 10.0451; 8.1208
90; 95.19; 90
1124.63Yuan, Guohao; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki
Highly Proton-Conducting Mixed Proton-Transferred [(H2PO4‒)(H3PO4)]∞Networks Supported by 2,2′-Diaminobithiazolium in Crystals
The Journal of Physical Chemistry C, 2020
1556992 CIFC18 H16 O4P b c n9.7263; 11.8883; 24.935
90; 90; 90
2883.2Liang, Kangjiang; Li, Tao; Li, Na; Zhang, Yang; Shen, Lei; Ma, Zhixian; Xia, Chengfeng
Redox-neutral photochemical Heck-type arylation of vinylphenols activated by visible light
Chemical Science, 2020, 11, 2130-2135
1556993 CIFC26 H24 N2 O2 SP -110.6565; 11.1408; 12.3
69.374; 76.912; 65.303
1236.26Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556994 CIFC28 H26 N2P 21 21 219.072; 9.846; 23.918
90; 90; 90
2136.4Lee, Jiyoun; Ko, Donguk; Park, Hyunju; Yoo, Eun Jeong
Direct cyclopropanation of activated N-heteroarenes <i>via</i> site- and stereoselective dearomative reactions.
Chemical science, 2020, 11, 1672-1676
1556995 CIFC54 H31.2 F0.8 O8 Zn2C 1 2/c 137.1066; 31.0733; 11.8903
90; 99.208; 90
13533.1Lustig, William P.; Shen, Zeqing; Teat, Simon J.; Javed, Nasir; Velasco, Ever; O'Carroll, Deirdre M.; Li, Jing
Rational design of a high-efficiency, multivariate metal‒organic framework phosphor for white LED bulbs
Chemical Science, 2020, 11, 1814-1824
1557016 CIFC22 H30 O2P 1 21/n 19.223; 6.718; 15.694
90; 90.983; 90
972.3Shu, Zhibin; Zhang, Qing; Zhang, Pan; Qin, Zhengsheng; Liu, Dan; Gao, Xiong; Guan, Bo; Qi, Haoyuan; Xiao, Mengqi; Wei, Zhongming; Dong, Huanli; Hu, Wenping
Preparing two-dimensional crystalline conjugated polymer films by synergetic polymerization and self-assembly at air/water interface
Polymer Chemistry, 2020, 11, 1572-1579
1557022 CIFC4 H18 Br5 N3 Pb S2P 1 21 110.066; 8.4068; 10.9787
90; 104.155; 90
900.8Bakthavatsalam, Rangarajan; Haris, Muhammed P. U.; Shaikh, Samir R.; Lohar, Amruta; Mohanty, Ashutosh; Moghe, Dhanashree; Sharma, Shivani; Biswas, Chinmoy; Raavi, Sai Santhosh Kumar; Gonnade, Rajesh G.; Kundu, Janardan
Ligand Structure Directed Dimensionality Reduction (2D →1D) in Lead Bromide Perovskite
The Journal of Physical Chemistry C, 2020
1557023 CIFC3 H11 Br4 N3 Pb SP 1 21/c 113.3113; 8.5838; 12.0368
90; 90.406; 90
1375.31Bakthavatsalam, Rangarajan; Haris, Muhammed P. U.; Shaikh, Samir R.; Lohar, Amruta; Mohanty, Ashutosh; Moghe, Dhanashree; Sharma, Shivani; Biswas, Chinmoy; Raavi, Sai Santhosh Kumar; Gonnade, Rajesh G.; Kundu, Janardan
Ligand Structure Directed Dimensionality Reduction (2D →1D) in Lead Bromide Perovskite
The Journal of Physical Chemistry C, 2020
1557024 CIFC38 H34 S4C 1 2/c 141.708; 5.7563; 12.67
90; 98.46; 90
3008.8Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557025 CIFC42 H42 S4P 1 21/c 123.82; 5.837; 12.5
90; 104.133; 90
1685Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557026 CIFC42 H42 S4P 1 21/c 122.15; 5.7413; 13.1188
90; 95.85; 90
1659.6Suzuki, Mitsuharu; Terai, Kengo; Quinton, Cassandre; Hayashi, Hironobu; Aratani, Naoki; Yamada, Hiroko
Open-circuit-voltage shift of over 0.5 V in organic photovoltaic cells induced by a minor structural difference in alkyl substituents
Chemical Science, 2020, 11, 1825-1831
1557027 CIFC66 H30 Al3 Ba F89 O9P 1 c 128.173; 16.4313; 20.453
90; 90.107; 90
9468.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557028 CIFC52 H26 Al2 Ca F68 O7P 1 21 117.765; 20.654; 20.031
90; 93.018; 90
7340Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557029 CIFC36 H18 Al2 F55 In O6P -110.6319; 22.3961; 24.4869
79.144; 79.696; 77.759
5537.2Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557030 CIFC50 H22 Al2 F74 Mg N6 O8P 114.3953; 18.2606; 25.8315
73.784; 74.37; 66.821
5895.1Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557031 CIFC84 H34 Al4 F118 O12 SrP -113.8661; 20.2883; 23.0336
80.031; 85.985; 79.942
6278.6Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557032 CIFC84 H34 Al4 Ca F118 O12P -113.9542; 20.3286; 22.9128
80.085; 84.743; 80.239
6296.8Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557033 CIFC60 H26 Al3 Ca F87 O9P 1 21/c 123.429; 18.9075; 22.4874
90; 118.27; 90
8773.4Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557034 CIFC66 H30 Al3 F89 O9 SrP -113.5412; 25.3825; 27.3385
90.017; 90.111; 92.474
9387.7Schorpp, Marcel; Krossing, Ingo
Soft interactions with hard Lewis acids: generation of mono- and dicationic alkaline-earth metal arene-complexes by direct oxidation.
Chemical science, 2020, 11, 2068-2076
1557040 CIFC17 H10 Br2 N2 OP 1 21/n 110.0349; 8.3874; 17.4347
90; 91.005; 90
1467.2Sala, Samuele; Nealon, Gareth L.; Sobolev, Alexandre N.; Fromont, Jane; Gomez, Oliver; Flematti, Gavin R.
Structure Reassignment of Echinosulfone A and the Echinosulfonic Acids A-D Supported by Single-Crystal X-ray Diffraction and Density Functional Theory Analysis.
Journal of natural products, 2020, 83, 105-110
1557041 CIFC40 H49 Br N2 OP 1 21/n 111.1088; 21.1979; 15.9518
90; 108.641; 90
3559.32Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557042 CIFC42 H44 N2 Ni O3P -110.35522; 11.18263; 16.4194
100.307; 95.6535; 99.0466
1831.63Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557043 CIFC46 H52 Au Cl N2P 1 21/c 112.2795; 16.812; 19.2885
90; 93.6946; 90
3973.7Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557044 CIFC39 H44 N2I 41/a :238.4682; 38.4682; 9.5772
90; 90; 90
14172.4Rottschäfer, Dennis; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
A crystalline C5-protonated 1,3-imidazol-4-ylidene.
Chemical communications (Cambridge, England), 2020, 56, 2027-2030
1557045 CIFC17 H14 Cl N O2P 21 21 215.3182; 10.94; 23.9705
90; 90; 90
1394.63Burg, Finn; Breitenlechner, Stefan; Jandl, Christian; Bach, Thorsten
Enantioselective oxygenation of exocyclic methylene groups by a manganese porphyrin catalyst with a chiral recognition site
Chemical Science, 2020, 11, 2121-2129
1557052 CIFC22 H28 NP -15.899; 7.547; 20.535
83.465; 84.681; 82.512
897.7Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557053 CIFC28 H18 O2P 1 21/c 113.0175; 9.329; 8.3512
90; 106.37; 90
973.06Mongin, Cédric; Ardoy, Alejandro Mendez; Méreau, Raphaël; Bassani, Dario M.; Bibal, Brigitte
Singlet oxygen stimulus for switchable functional organic cages
Chemical Science, 2020, 11, 1478-1484
1557054 CIFC20 H14 I NP c c n16.5305; 18.7386; 10.5281
90; 90; 90
3261.2Martinez, Thibaut; Alahyen, Ismail; Lemière, Gilles; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Straightforward Access to 2-Iodoindolizines via Iodine-Mediated Cyclization of 2-Pyridylallenes
Organic Process Research & Development, 2020
1557055 CIFC20 H21 B Cl2 O2C 1 2/c 127.001; 6.0841; 25.1455
90; 108.298; 90
3922Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557056 CIFC22 H27 B O2C 1 2/c 135.07; 6.2286; 20.596
90; 119.212; 90
3926.8Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557057 CIFC22 H27 B O2P c a 2125.447; 6.3811; 24.281
90; 90; 90
3942.7Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557058 CIFC36.5 H57 B Cl F4 N4 P4 RhP 31 2 113.824; 13.824; 40.089
90; 90; 120
6635Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557059 CIFC27 H42 B Cl2 F4 N2 P2 RhP 1 21 19.7105; 14.3281; 11.2851
90; 96.031; 90
1561.44Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557060 CIFC18 H19 N S SiP -18.52831; 10.39109; 11.21545
117.584; 92.3119; 95.1854
873.5Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557061 CIFC17 H13 N O SC 1 2/c 120.6204; 9.4103; 16.7239
90; 120.205; 90
2804.6Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557062 CIFC18 H15 N O SP b c a13.1964; 13.3812; 16.7048
90; 90; 90
2949.79Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557063 CIFC11 H9 N O SP 1 21/c 110.9143; 7.26579; 12.4737
90; 104.425; 90
957.99Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557064 CIFC16 H21 N S Se SiP 1 21/c 110.6588; 8.0663; 20.1272
90; 95.886; 90
1721.35Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557065 CIFC22 H23 N SP 1 21/c 113.9373; 7.7203; 17.0136
90; 105.984; 90
1759.89Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557066 CIFC21 H20 SP 1 21/n 17.5133; 25.6215; 8.2645
90; 100.591; 90
1563.83Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557067 CIFC10 H7 N SP -16.9027; 7.3743; 9.3503
68.861; 73.292; 84.246
425.18Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557068 CIFC16 H11 N O SP b c a12.2557; 9.5626; 21.5616
90; 90; 90
2526.94Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557069 CIFC17 H17 N SP 1 21/c 111.1885; 11.263; 12.1884
90; 116.756; 90
1371.48Bürger, Marcel; Loch, Maximilian N.; Jones, Peter G.; Werz, Daniel B.
From 1,2-difunctionalisation to cyanide-transfer cascades ‒ Pd-catalysed cyanosulfenylation of internal (oligo)alkynes
Chemical Science, 2020, 11, 1912-1917
1557075 CIFC55 H67 N3 O6 P2 RuP 1 21/n 117.5623; 13.934; 20.8795
90; 92.113; 90
5106Artús Suàrez, Lluís; Jayarathne, Upul; Balcells, David; Bernskoetter, Wesley H.; Hazari, Nilay; Jaraiz, Martín; Nova, Ainara
Rational selection of co-catalysts for the deaminative hydrogenation of amides.
Chemical science, 2020, 11, 2225-2230
1557079 CIFC25 H23 N O3P 1 21 112.77764; 5.95718; 12.86001
90; 100.546; 90
962.352Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557080 CIFC23 H29 N O2P 21 21 2110.3193; 10.5258; 18.2046
90; 90; 90
1977.36Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557081 CIFC25 H25 N O3 SP 21 21 215.909; 12.8175; 27.4929
90; 90; 90
2082.27Di Sanza, Riccardo; Nguyen, Thi Le Nhon; Iqbal, Naeem; Argent, Stephen P.; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative and alkenylative intramolecular 1,2-allylations of tethered allene‒ketones
Chemical Science, 2020, 11, 2401-2406
1557082 CIFC24 H18 O3C 1 2/c 121.613; 12.1859; 13.5922
90; 104.043; 90
3472.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557083 CIFC26 H24 O6P 1 21/c 114.145; 7.441; 24.56
90; 96.17; 90
2570He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557084 CIFC22 H15 Cl O3P 1 21/n 116.2589; 6.7715; 16.4568
90; 106.511; 90
1737.14He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557085 CIFC25 H24 O7P 1 21/n 112.5579; 5.2167; 35.021
90; 94.917; 90
2285.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557086 CIFC25 H28 O8C 1 2/c 129.9022; 11.0935; 13.4816
90; 99.73; 90
4407.8He, Zhen; Perry, Gregory J. P.; Procter, David J.
Sulfoxide-mediated oxidative cross-coupling of phenols
Chemical Science, 2020, 11, 2001-2005
1557087 CIFC39 H34 F6 N3 O PP 1 21/c 19.3923; 29.4208; 11.9664
90; 102.511; 90
3228.14Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557088 CIFC27 H22 N2 OP 1 21/n 19.53897; 23.141; 9.5721
90; 107.33; 90
2017.04Zheng, Zheng; Liu, Haixiang; Zhai, Shaodong; Zhang, Haoke; Shan, Guogang; Kwok, Ryan T. K.; Ma, Chao; Sung, Herman H. Y.; Williams, Ian D.; Lam, Jacky W. Y.; Wong, Kam Sing; Hu, Xianglong; Tang, Ben Zhong
Highly efficient singlet oxygen generation, two-photon photodynamic therapy and melanoma ablation by rationally designed mitochondria-specific near-infrared AIEgens
Chemical Science, 2020, 11, 2494-2503
1557089 CIFC78 H190 Dy2 K2 N6 O21 Si12C 1 2/c 125.4899; 18.8304; 25.7453
90; 103.128; 90
12034.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557090 CIFC42 H102 Dy K N3 O12 Si6P 1 21/n 111.0616; 27.199; 21.7721
90; 103.885; 90
6359Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557091 CIFC78 H190 K2 N6 O21 Si12 Tm2C 1 2/c 125.453; 18.757; 25.744
90; 103.142; 90
11969Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557092 CIFC42 H102 K N3 O12 Si6 TmP 21 21 2121.956; 22.554; 25.737
90; 90; 90
12745Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557093 CIFC52 H124 Gd2 K2 N4 O16 Si8P -112.6614; 15.5498; 21.205
94.4758; 94.0831; 105.746
3987.4Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557094 CIFC36 H90 Gd K N5 O6 Si6R 3 2 :H18.564; 18.564; 18.05
90; 90; 120
5387Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557095 CIFC42 H102 Er K N3 O12 Si6P 1 21/n 111.064; 27.08; 21.797
90; 103.991; 90
6337Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557096 CIFC42 H102 Ho K N3 O12 Si6P 1 21/n 111.0476; 27.157; 21.797
90; 103.905; 90
6347.9Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557097 CIFC42 H102 Gd K N3 O12 Si6P 1 21/n 111.1493; 27.059; 21.755
90; 104.007; 90
6368.1Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557098 CIFC42 H102 K N3 O12 Si6 TbP 1 21/n 111.1324; 27.081; 21.775
90; 103.924; 90
6371.8Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557099 CIFC78 H190 Gd2 K2 N6 O21 Si12C 1 2/c 125.507; 18.806; 25.726
90; 103.21; 90
12014Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557100 CIFC42 H102 K N3 O12 Si6 YP 1 21/n 111.0774; 27.0905; 21.7959
90; 104; 90
6346.5Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557101 CIFC78 H190 Ho2 K2 N6 O21 Si12C 1 2/c 125.514; 18.8; 25.712
90; 103.167; 90
12009Ryan, Austin J.; Ziller, Joseph W.; Evans, William J.
The importance of the counter-cation in reductive rare-earth metal chemistry: 18-crown-6 instead of 2,2,2-cryptand allows isolation of [YII(NR2)3]1− and ynediolate and enediolate complexes from CO reactions
Chemical Science, 2020, 11, 2006-2014
1557105 CIFC104 H96 B4 F16 N8 O4 Pd2I 1 2/a 128.36; 12.35285; 27.666
90; 94.6541; 90
9660.2Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557106 CIFC123 H119 B4 F16 N17 O9 Pd2C 1 2/c 123.2193; 15.8896; 38.7298
90; 112.281; 90
13222.3Lewis, James E. M.; Tarzia, Andrew; White, Andrew J. P.; Jelfs, Kim E.
Conformational control of Pd2L4 assemblies with unsymmetrical ligands
Chemical Science, 2020, 11, 677-683
1557107 CIFC16 H19 I N2P 1 21/c 16.29025; 7.62301; 32.0065
90; 90.1584; 90
1534.73Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557108 CIFC64 H87 I3 N5 O2P -114.6729; 15.6807; 16.4518
85.945; 73.88; 62.636
3222.3Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557109 CIFC17 H18 I N2P 21 21 216.9063; 7.9318; 30.157
90; 90; 90
1651.98Guo, Lifang; Li, Chuanya; Shang, Hai; Zhang, Ruoyao; Li, Xuechen; Lu, Qing; Cheng, Xiao; Liu, Zhiqiang; Sun, Jing Zhi; Yu, Xiaoqiang
A side-chain engineering strategy for constructing fluorescent dyes with direct and ultrafast self-delivery to living cells
Chemical Science, 2020, 11, 661-670
1557110 CIFC73 H92 N5 O2 UP -113.2857; 13.9411; 20.5686
103.573; 95.666; 116.252
3230.4Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557111 CIFC75 H88 N8 UP -113.1219; 13.5561; 20.3099
78.109; 76.264; 68.201
3230.5Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557112 CIFC76 H99 N6 O P UP 1 21/c 125.884; 13.889; 21.315
90; 110.09; 90
7197Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557113 CIFC75 H96 N6 UP 1 21/n 114.7113; 12.979; 36.748
90; 94.521; 90
6994.8Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557114 CIFC82 H101 N7 O UP -113.1812; 15.8571; 19.6743
110.71; 90.48; 105.002
3692.6Yadav, Munendra; Metta-Magaña, Alejandro; Fortier, Skye
Intra- and intermolecular interception of a photochemically generated terminal uranium nitride
Chemical Science, 2020, 11, 2381-2387
1557115 CIFC33 H26 O2P 21 21 2111.3659; 11.9259; 17.9314
90; 90; 90
2430.58Liu, Xihong; Zhang, Jingying; Bai, Lutao; Wang, Linqing; Yang, Dongxu; Wang, Rui
Catalytic asymmetric multiple dearomatizations of phenols enabled by a cascade 1,8-addition and Diels‒Alder reaction
Chemical Science, 2020, 11, 671-676
1557116 CIFC64 H88P -114.635; 18.1373; 22.0161
79.631; 75.201; 74.12
5396.2Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057
1557117 CIFC61 H39 B F24 N7 RhP -112.9083; 14.2464; 20.148
74.898; 79.351; 89.459
3512.7Storey, Caroline M.; Kalpokas, Audrius; Gyton, Matthew R.; Krämer, Tobias; Chaplin, Adrian B.
A shape changing tandem Rh(CNC) catalyst: preparation of bicyclo[4.2.0]octa-1,5,7-trienes from terminal aryl alkynes.
Chemical science, 2020, 11, 2051-2057

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