Crystallography Open Database

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7126211 CIFC53 H126 Fe9 N6 O6R 3 2 :H16.9429; 16.9429; 23.233
90; 90; 120		5775.8Kephart, Jonathan A.; Hecht, Zachary; Livesay, Brooke N.; Bhowmick, Indrani; Shores, Matthew P.; Popescu, V. Codrina; Arulsamy, Navamoney; Hulley, Elliott B.
Self-assembly of an organometallic Fe<sub>9</sub>O<sub>6</sub> cluster from aerobic oxidation of (tmeda)Fe(CH<sub>2</sub><sup>t</sup>Bu)<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 4994-4997
7126212 CIFC24 H19 Br F3 N O2P -18.262; 11.3867; 22.2514
91.776; 94.224; 94.328		2080.3Huang, Jie; Li, Feng; Cui, Lei; Su, Shikuan; Jia, Xueshun; Li, Jian
Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application.
Chemical communications (Cambridge, England), 2020, 56, 4555-4558
7126213 CIFC34 H27 Br3 N2 O5P 1 21/n 110.8209; 13.1614; 23.1775
90; 103.056; 90		3215.6Huang, Jie; Li, Feng; Cui, Lei; Su, Shikuan; Jia, Xueshun; Li, Jian
Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application.
Chemical communications (Cambridge, England), 2020, 56, 4555-4558
7126214 CIFC7 H25 I8 N11 Sn2P -19.353; 12.8318; 15.0588
111.452; 102.192; 91.234		1634.4McNulty, Jason A.; Lightfoot, Philip
Unprecedented tin iodide perovskite-like structures featuring ordering of organic moieties.
Chemical communications (Cambridge, England), 2020, 56, 4543-4546
7126215 CIFC3 H10 I6 N6 Sn2P 43 21 29.0746; 9.0746; 25.3561
90; 90; 90		2088McNulty, Jason A.; Lightfoot, Philip
Unprecedented tin iodide perovskite-like structures featuring ordering of organic moieties.
Chemical communications (Cambridge, England), 2020, 56, 4543-4546
7126216 CIFC47 H50 Al F36 N5 O4 SiP 1 21/m 110.8558; 19.5631; 14.1328
90; 97.318; 90		2976.98Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126217 CIFC48 H49 Al Cl2 F36 N4 O4 SiP 1 21 110.8096; 36.2399; 15.9889
90; 92.324; 90		6258.32Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126218 CIFC57 H72 Al F36 N5 O4 SnP 1 21 111.0279; 19.9344; 17.9479
90; 107.293; 90		3767.22Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126219 CIFC47 H47 Al F36 N4 O4 SiP 1 21/c 113.993; 19.5525; 21.6682
90; 98.012; 90		5870.51Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126220 CIFC51 H58 Al F36 Ge N5 O4P -111.2303; 14.7524; 20.0867
80.757; 87.515; 86.337		3276.07Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126221 CIFC47 H47 Al F36 Ge N4 O4P 1 21/c 113.9314; 19.6837; 21.7403
90; 98.072; 90		5902.59Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126222 CIFC51 H58 Al F36 N5 O4 SiP -111.1801; 14.7647; 20.0683
82.558; 87.937; 85.473		3273.4Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126223 CIFC47 H47 Al F36 N4 O4 SnP 1 21/n 116.261; 19.8055; 18.8111
90; 103.171; 90		5898.88Do, Dinh Cao Huan; Protchenko, Andrey V.; Fuentes, M Ángeles; Hicks, Jamie; Vasko, Petra; Aldridge, Simon
N-H cleavage vs. Werner complex formation: reactivity of cationic group 14 tetrelenes towards amines.
Chemical communications (Cambridge, England), 2020, 56, 4684-4687
7126224 CIFC34 H22 F10 I2 N2 O S2P n a 2117.2715; 27.171; 7.9406
90; 90; 90		3726.4Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126225 CIFC31 H18 F10 I2 N2 O S2P n a 2117.564; 25.64; 7.07
90; 90; 90		3184Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126226 CIFC31 H16 F10 I2 N2 S2P n a 2117.723; 26.15; 7
90; 90; 90		3244Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126227 CIFC31 H16 F10 I2 N2 S2P n a 2117.556; 26.464; 7.633
90; 90; 90		3546Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126228 CIFC33.85 H24 F10 I2 N2 O2 S2P n a 2117.2451; 27.2415; 7.9554
90; 90; 90		3737.3Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126229 CIFC31 H16 F10 I2 N2 S2P n a 2117.449; 26.511; 7.536
90; 90; 90		3486Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126230 CIFC31 H18 F10 I2 N2 O S2P n a 2117.606; 25.58; 6.944
90; 90; 90		3127Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126231 CIFC31 H16 F10 I2 N2 S2P n a 2117.559; 26.315; 7.259
90; 90; 90		3354Sobczak, Szymon; Półrolniczak, Aleksandra; Ratajczyk, Paulina; Cai, Weizhao; Gładysiak, Andrzej; Nikolayenko, Varvara I.; Castell, Dominic C.; Barbour, Leonard J.; Katrusiak, Andrzej
Large negative linear compressibility of a porous molecular co-crystal.
Chemical communications (Cambridge, England), 2020, 56, 4324-4327
7126232 CIFC24 H24 Cl3 F N O2 PP 1 21/c 113.7106; 10.0817; 19.9799
90; 91.438; 90		2760.88Gou, Xue-Ya; Zhang, Bo-Sheng; Wang, Xin-Gang; Shi, Wei-Yu; Liu, Hong-Chao; An, Yang; Zhang, Zhe; Liang, Yong-Min
Visible-light-induced ligand-free RuCl<sub>3</sub> catalyzed C-H phosphorylation in water.
Chemical communications (Cambridge, England), 2020, 56, 4704-4707
7126233 CIFC66 H88 Li2 N2 O5P 1 21 112.845; 16.759; 14.762
90; 107.779; 90		3026Schmidlin, Nadja M. C.; Scherer, Harald; Hoffmann, Anke; Böttcher, Tobias
Isolation and characterization of a lithiated pyridine - aggregation in the solid state and in solution.
Chemical communications (Cambridge, England), 2020, 56, 4160-4163
7126234 CIFC16 H16 O6P 1 21/n 18.17188; 12.40101; 13.7935
90; 91.4883; 90		1397.36Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126235 CIFC16 H16 O6P 21 21 219.1094; 10.3354; 14.8756
90; 90; 90		1400.53Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126236 CIFC16 H18 O7P 1 21/c 113.4502; 7.6047; 15.7124
90; 110.641; 90		1504Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126237 CIFC16 H16 O6P 1 21/n 18.519; 16.0695; 10.3653
90; 102.495; 90		1385.4Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126238 CIFC16 H16 O6P 1 21/n 19.17259; 11.667; 12.81692
90; 98.1439; 90		1357.79Chen, Guo-Dong; Hu, Dan; Huang, Mei-Juan; Tang, Jia; Wang, Xiao-Xia; Zou, Jian; Xie, Jun; Zhang, Wei-Guang; Guo, Liang-Dong; Yao, Xin-Sheng; Abe, Ikuro; Gao, Hao
Sporormielones A-E, bioactive novel C-C coupled orsellinic acid derivative dimers, and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 4607-4610
7126239 CIFC65 H72 B F24 P2 RhP 1 21/n 119.0415; 17.9747; 19.5602
90; 91.7586; 90		6691.62Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126240 CIFC61 H66 B F24 P2 RhP -112.8015; 12.9012; 19.8814
91.347; 90.717; 96.597		3260.5Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126241 CIFC62 H70 B F24 O P2 RhP -112.877; 13.5514; 19.2488
91.699; 95.671; 98.347		3303.8Bukvic, Alexander J.; Crivoi, Dana Georgiana; Garwood, Hollie G.; McKay, Alasdair I.; Chen, Thomas T. D.; Martínez-Martínez, Antonio J; Weller, Andrew S.
Tolerant to air σ-alkane complexes by surface modification of single crystalline solid-state molecular organometallics using vapour-phase cationic polymerisation: SMOM@polymer.
Chemical communications (Cambridge, England), 2020, 56, 4328-4331
7126242 CIFC40 H104 B4 Na2 O2 Si8 Y2P -110.929; 16.497; 17.2819
90.747; 90.198; 92		3113.7Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126243 CIFC40 H104 B4 Dy2 Na2 O2 Si8P -110.9592; 16.5329; 17.2892
90.676; 90.257; 92.791		3128.6Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126244 CIFC20 H52 B2 Dy K O Si4P 1 21/n 110.846; 17.5547; 16.9092
90; 91.916; 90		3217.68Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126245 CIFC20 H52 B2 K O Si4 YP 1 21/n 110.7817; 17.5986; 16.9013
90; 91.955; 90		3205.03Durrant, James P.; Tang, Jinkui; Mansikkamäki, Akseli; Layfield, Richard A.
Enhanced single-molecule magnetism in dysprosium complexes of a pristine cyclobutadienyl ligand.
Chemical communications (Cambridge, England), 2020, 56, 4708-4711
7126246 CIFC30 H19 B F20 Ge O2P b c a14.3032; 17.5925; 24.968
90; 90; 90		6282.7Talavera, Maria; Meißner, Gisa; Rachor, Simon G.; Braun, Thomas
C-F activation reactions at germylium ions: dehydrofluorination of fluoralkanes.
Chemical communications (Cambridge, England), 2020, 56, 4452-4455
7126247 CIFC14 H13 N O4 SP 1 21 17.7349; 9.6402; 9.3298
90; 101.782; 90		681Liu, Gongyi; Zhang, Xianghe; Wang, Heng; Cong, Hengjiang; Zhang, Xumu; Dong, Xiu-Qin
Synthesis of chiral α-substituted α-amino acid and amine derivatives through Ni-catalyzed asymmetric hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 4934-4937
7126248 CIFC9 H11 N O5 SP 31 2 17.1576; 7.1576; 37.3509
90; 90; 120		1657.17Liu, Gongyi; Zhang, Xianghe; Wang, Heng; Cong, Hengjiang; Zhang, Xumu; Dong, Xiu-Qin
Synthesis of chiral α-substituted α-amino acid and amine derivatives through Ni-catalyzed asymmetric hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 4934-4937
7126249 CIFC22 H14 N2 O5P 1 21/n 112.7979; 5.74316; 22.89076
90; 92.3207; 90		1681.1Aizawa, Takumi; Aratsu, Keisuke; Datta, Sougata; Mashimo, Takaki; Seki, Tomohiro; Kajitani, Takashi; Silly, Fabien; Yagai, Shiki
Hydrogen bond-directed supramolecular polymorphism leading to soft and hard molecular ordering.
Chemical communications (Cambridge, England), 2020, 56, 4280-4283
7126250 CIFC4 H12 Cl2 Ga NP -4 21 m9.2755; 9.2755; 5.8368
90; 90; 90		502.17Wu, Qi; Liu, Xian; Du, Yeshuang; Teng, Chunlin; Liang, Fei
Nonlinear organic-inorganic halide hybrids containing unprecedented linear [MIX<sub>2</sub>]<sup>-</sup> coordination units and quasi-two-dimensional lone pairs.
Chemical communications (Cambridge, England), 2020, 56, 4894-4897
7126251 CIFC4 H12 Cl2 In NP -4 21 m9.2807; 9.2807; 5.8414
90; 90; 90		503.128Wu, Qi; Liu, Xian; Du, Yeshuang; Teng, Chunlin; Liang, Fei
Nonlinear organic-inorganic halide hybrids containing unprecedented linear [MIX<sub>2</sub>]<sup>-</sup> coordination units and quasi-two-dimensional lone pairs.
Chemical communications (Cambridge, England), 2020, 56, 4894-4897
7126252 CIFC14 H10 Cl N O SP 1 21/c 19.0173; 9.8035; 14.1588
90; 95.552; 90		1245.8Pradhan, Suman; Patel, Sandeep; Chatterjee, Indranil
Nitrosoarene-catalyzed regioselective aromatic C-H sulfinylation with thiols under aerobic conditions.
Chemical communications (Cambridge, England), 2020, 56, 5054-5057
7126253 CIFC14 H15 N O SP 1 21/c 114.275; 7.6981; 11.6398
90; 101.25; 90		1254.5Pradhan, Suman; Patel, Sandeep; Chatterjee, Indranil
Nitrosoarene-catalyzed regioselective aromatic C-H sulfinylation with thiols under aerobic conditions.
Chemical communications (Cambridge, England), 2020, 56, 5054-5057
7126254 CIFC141 H244 N12 U4P 42 21 220.7855; 20.7855; 35.3744
90; 90; 90		15283.1Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126255 CIFC55.5 H62 B F15 N UP -112.5562; 13.4735; 18.1929
100.421; 97.392; 116.686		2626.3Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126256 CIFC52 H40 B2 F30 N6 Na2 O4P -111.1153; 11.7453; 12.4529
70.938; 81.452; 72.255		1461.32Boreen, Michael A.; Rao, Guodong; Villarreal, David G.; Watt, Fabian A.; Britt, R. David; Hohloch, Stephan; Arnold, John
Lewis acid capping of a uranium(v) nitride via a uranium(iii) azide molecular square.
Chemical communications (Cambridge, England), 2020, 56, 4535-4538
7126257 CIFC60 H61 N5 O8P -18.9154; 9.9908; 14.3287
98.926; 91.79; 92.209		1259Ren, Demin; Koniarz, Sebastian; Li, Xiaofang; Chmielewski, Piotr J.
First imidazole-fused carbaporphyrinoid and its conversion to a N-heterocyclic carbene precursor.
Chemical communications (Cambridge, England), 2020, 56, 4836-4839
7126258 CIFC48.5 H33 Ag Au Cl4 N5P -19.9193; 13.7034; 15.7321
75.013; 84.724; 78.55		2022.72Ren, Demin; Koniarz, Sebastian; Li, Xiaofang; Chmielewski, Piotr J.
First imidazole-fused carbaporphyrinoid and its conversion to a N-heterocyclic carbene precursor.
Chemical communications (Cambridge, England), 2020, 56, 4836-4839
7126259 CIFC18 H11 Cr F9 N3 O9 S3P -113.3872; 13.4166; 15.684
81.472; 68.974; 85.355		2599.2Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126260 CIFC43 H26 Cr F6 N10 O6 S2P -19.863; 12.837; 16.567
98.505; 100.19; 98.845		2006.6Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126261 CIFC94 H75 Cr2 F6 N21 O8 S2P -110.8374; 13.4385; 15.1456
81.115; 87.233; 76.72		2120.85Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126262 CIFC46 H33 Cr F9 N9 O10 S3P -110.6856; 13.1212; 18.0622
72.344; 83.075; 86.981		2395.2Ma, Xiaozhou; Suturina, Elizaveta A.; Rouzières, Mathieu; Wilhelm, Fabrice; Rogalev, Andrei; Clérac, Rodolphe; Dechambenoit, Pierre
A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange.
Chemical communications (Cambridge, England), 2020, 56, 4906-4909
7126263 CIFC42 H50 O4 SP 1 21/c 117.0878; 10.7963; 21.0437
90; 109.074; 90		3669.1Ghotekar, Ganesh S.; Shirsath, Sachin R.; Shaikh, Aslam C.; Muthukrishnan, M.
1,6-Conjugate addition initiated formal [4+2] annulation of p-quinone methides with sulfonyl allenols: a unique access to spiro[5.5]undeca-1,4-dien-3-one scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 5022-5025
7126264 CIFC32 H31 F N2 O4 S2P 1 21/n 111.5515; 15.2491; 15.9658
90; 91.512; 90		2811.4Wang, Hao-Ran; Huang, En-He; Luo, Chen; Luo, Wen-Feng; Xu, Yin; Qian, Peng-Cheng; Zhou, Jin-Mei; Ye, Long-Wu
Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids.
Chemical communications (Cambridge, England), 2020, 56, 4832-4835
7126265 CIFC28 H23 N O3 SP 1 21/c 112.7799; 10.1536; 18.2019
90; 108.934; 90		2234.12Wang, Hao-Ran; Huang, En-He; Luo, Chen; Luo, Wen-Feng; Xu, Yin; Qian, Peng-Cheng; Zhou, Jin-Mei; Ye, Long-Wu
Copper-catalyzed tandem cis-carbometallation/cyclization of imine-ynamides with arylboronic acids.
Chemical communications (Cambridge, England), 2020, 56, 4832-4835
7126266 CIFC22 H16 F6 N2 O2P b c n28.1272; 9.04947; 14.7304
90; 90; 90		3749.42Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126267 CIFC20 H18 N2 O2P 1 21/n 17.16584; 10.4417; 21.8016
90; 96.8756; 90		1619.54Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126268 CIFC10 H12.67 N0.67 O1.33C 1 2/c 117.8343; 12.4405; 13.0921
90; 107.301; 90		2773.29Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126269 CIFC22 H22 N2 O4P -17.3701; 10.2836; 12.5573
97.383; 104.649; 99.61		893.22Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126270 CIFC28 H34 N2 O2P 1 21/c 116.29085; 20.8151; 23.2057
90; 105.286; 90		7590.55Lamb, Katie J.; Dowsett, Mark R.; North, Michael; Parker, Rachel R.; Whitwood, Adrian C.
Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation.
Chemical communications (Cambridge, England), 2020, 56, 4844-4847
7126271 CIFC120 H174 B2 Ca2 N12 O2P 1 2/c 115.552; 15.578; 45.215
90; 90.58; 90		10954Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126272 CIFC62 H83 B Ca N6P -111.9771; 14.8686; 16.6034
99.757; 99.777; 104.406		2751.9Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126273 CIFC62 H83 B Ca N6P -111.7488; 15.0579; 15.7679
96.695; 94.947; 101.734		2695.2Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126274 CIFC63 H93 B Ca N6 OP -114.5913; 14.6823; 15.1498
61.123; 82.567; 88.425		2815.9Shi, Xianghui; Hou, Cuiping; Zhao, Lanxiao; Deng, Peng; Cheng, Jianhua
Mononuclear calcium complex as effective catalyst for alkenes hydrogenation.
Chemical communications (Cambridge, England), 2020, 56, 5162-5165
7126275 CIFC74 H50 Cd N4 O8C 1 2/c 124.4932; 13.5736; 18.0604
90; 97.554; 90		5952.3Yang, Yongsheng; Fang, Xiaoyu; Zhao, Si-Si; Bai, Fengyang; Zhao, Zhen; Wang, Ke-Zhi; Yan, Dongpeng
One-dimensional co-crystallized coordination polymers showing reversible mechanochromic luminescence: cation-anion interaction directed rapid self-recovery.
Chemical communications (Cambridge, England), 2020, 56, 5267-5270
7126276 CIFC30 H22 Cd O6P n c a7.5033; 16.7674; 19.8262
90; 90; 90		2494.35Yang, Yongsheng; Fang, Xiaoyu; Zhao, Si-Si; Bai, Fengyang; Zhao, Zhen; Wang, Ke-Zhi; Yan, Dongpeng
One-dimensional co-crystallized coordination polymers showing reversible mechanochromic luminescence: cation-anion interaction directed rapid self-recovery.
Chemical communications (Cambridge, England), 2020, 56, 5267-5270
7126277 CIFC44 H43 N2 O12 S2P -19.2048; 15.0598; 16.5389
116.533; 90.512; 99.24		2016.11Tian, Tian; Qian, Tingjuan; Jiang, Tingting; Deng, Yakui; Li, Xiaopei; Yuan, Wei; Chen, Yulan; Wang, Yi-Xuan; Hu, Wenping
A donor-acceptor type macrocycle: toward photolyzable self-assembly.
Chemical communications (Cambridge, England), 2020, 56, 3939-3942
7126278 CIFC31 H32 Cl2 Co F6 N12 O2 PP 1 21/n 111.2862; 20.4254; 21.7177
90; 124.766; 90		4112.8Fleming, Connor; Chung, Dorothy; Ponce, Servando; Brook, David J. R.; DaRos, Jeffrey; Das, Raja; Ozarowski, Andrew; Stoian, Sebastian A.
Valence tautomerism in a cobalt-verdazyl coordination compound.
Chemical communications (Cambridge, England), 2020, 56, 4400-4403
7126279 CIFC30 H30 Co F12 N12 O2 P2P -4 21 c15.7805; 15.7805; 15.4465
90; 90; 90		3846.6Fleming, Connor; Chung, Dorothy; Ponce, Servando; Brook, David J. R.; DaRos, Jeffrey; Das, Raja; Ozarowski, Andrew; Stoian, Sebastian A.
Valence tautomerism in a cobalt-verdazyl coordination compound.
Chemical communications (Cambridge, England), 2020, 56, 4400-4403
7126280 CIFC12 H37 Ca N2 O17 P4C 1 2/c 131.0593; 5.1776; 21.8198
90; 130.591; 90		2664.6Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126281 CIFC12 H40 Mg N2 O18 P4P 1 21/c 114.681; 13.1202; 13.8859
90; 101.214; 90		2623.6Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126282 CIFC8 H28 Mg N2 O16 P4P 1 21/c 112.5897; 13.5306; 12.4892
90; 109.919; 90		2000.21Vassaki, Maria; Papathanasiou, Konstantinos E.; Hadjicharalambous, Chrystalleni; Chandrinou, Daphne; Turhanen, Petri; Choquesillo-Lazarte, Duane; Demadis, Konstantinos D.
Self-sacrificial MOFs for ultra-long controlled release of bisphosphonate anti-osteoporotic drugs.
Chemical communications (Cambridge, England), 2020, 56, 5166-5169
7126283 CIFC106 H62 F20 N8 O6 Sb2P 1 21/c 114.7806; 19.611; 32.18
90; 100.277; 90		9178.1Lemon, Christopher M.; Maher, Andrew G.; Mazzotti, Anthony R.; Powers, David C.; Gonzalez, Miguel I.; Nocera, Daniel G.
Multielectron C-H photoactivation with an Sb(v) oxo corrole.
Chemical communications (Cambridge, England), 2020, 56, 5247-5250
7126284 CIFC16 H22 Al1.33 Cl4 N2 O2C 1 2/c 122.483; 12.582; 24.213
90; 93.89; 90		6834Kore, Rajkumar; Kelley, Steven P.; Sawant, Anand D.; Mishra, Manish Kumar; Rogers, Robin D.
Are ionic liquids and liquid coordination complexes really different? - Synthesis, characterization, and catalytic activity of AlCl<sub>3</sub>/base catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5362-5365
7126285 CIFC8 H12 Al2 Cl6 N4P 1 21/n 18.4788; 11.2242; 9.6038
90; 91.3763; 90		913.71Kore, Rajkumar; Kelley, Steven P.; Sawant, Anand D.; Mishra, Manish Kumar; Rogers, Robin D.
Are ionic liquids and liquid coordination complexes really different? - Synthesis, characterization, and catalytic activity of AlCl<sub>3</sub>/base catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5362-5365
7126286 CIFC18 H19 N O3 SP -15.4468; 9.8135; 15.2598
103.033; 93.291; 97.938		783.72Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126287 CIFC13 H16 N O3.5 SC 1 2/c 131.768; 5.5762; 15.75
90; 108.619; 90		2644Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126288 CIFC17 H17 N O3 SP 1 21/c 116.352; 10.823; 9.736
90; 105.376; 90		1661Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126289 CIFC21 H19 N O3 SP 1 21/c 118.261; 7.799; 12.919
90; 107.2; 90		1758Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126290 CIFC17 H17 N O3 SP -15.432; 9.545; 15.32
96.31; 93.878; 97.64		779.8Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126291 CIFC18 H19 N O3 SP -15.8765; 7.649; 18.388
92.938; 94.963; 93.182		820.9Chakraborty, Poulami; Das, Bikash; Pal, Pulak; Datta, Subhadeep; Bera, Sourabh; Dastidar, Parthasarathi
A supramolecular hydrogel derived from a simple organic salt capable of proton conduction.
Chemical communications (Cambridge, England), 2020, 56, 5251-5254
7126292 CIFC112 H98 B F4 Ir2 O4 P4P 21 21 2115.3077; 17.0493; 35.2582
90; 90; 90		9201.9Sofue, Yuki; Nomura, Kotohiro; Inagaki, Akiko
On-demand hydrogen production from formic acid by light-active dinuclear iridium catalysts.
Chemical communications (Cambridge, England), 2020, 56, 4519-4522
7126293 CIFC7 H8 Fe K N7 OP 21 21 219.8433; 8.532; 14.8241
90; 90; 90		1244.97Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126294 CIFC7 H8 Fe K N7 OP 21 21 2110.2018; 8.5037; 14.948
90; 90; 90		1296.78Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126295 CIFC7 H8 Fe K N7 OP 21 21 219.9126; 8.5286; 14.8615
90; 90; 90		1256.4Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126296 CIFC7 H8 Fe K N7 OP 21 21 2110.0838; 8.515; 14.9235
90; 90; 90		1281.38Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126297 CIFC7 H8 Fe K N7 OP n m a10.3494; 8.4866; 14.9745
90; 90; 90		1315.23Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126298 CIFC7 H8 Fe K N7 OP n m a10.4242; 8.5078; 15.0275
90; 90; 90		1332.7Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126299 CIFC7 H8 Fe K N7 OP n m a10.3262; 8.4855; 14.9627
90; 90; 90		1311.08Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126300 CIFC7 H8 Fe K N7 OP 21 21 219.9983; 8.5234; 14.8981
90; 90; 90		1269.61Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126301 CIFC7 H8 Fe K N7 OP 21 21 2110.135; 8.5134; 14.9364
90; 90; 90		1288.76Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126302 CIFC7 H8 Fe K N7 OP n m a10.3809; 8.4936; 14.9835
90; 90; 90		1321.11Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126303 CIFC7 H8 Fe K N7 OP 21 21 2110.0402; 8.5197; 14.913
90; 90; 90		1275.65Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126304 CIFC7 H8 Fe K N7 OP n m a10.3982; 8.5036; 15.0131
90; 90; 90		1327.49Qiu, Rong-Guan; Chen, Xiao-Xian; Huang, Rui-Kang; Zhou, Dong-Dong; Xu, Wei-Jian; Zhang, Wei-Xiong; Chen, Xiao-Ming
Nitroprusside as a promising building block to assemble an organic-inorganic hybrid for thermo-responsive switching materials.
Chemical communications (Cambridge, England), 2020, 56, 5488-5491
7126305 CIFC11 H16 N2 O4P -16.8265; 7.2475; 13.022
87.473; 79.192; 79.227		621.65Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126306 CIFC10 H12 N2 O2P n a 218.872; 12.3858; 9.6316
90; 90; 90		1058.39Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126307 CIFC12 H10 N3 O2P n m a9.9477; 7.5082; 16.9603
90; 90; 90		1266.75Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126308 CIFC10 H13 N3 O5P -16.7495; 7.182; 14.8256
76.262; 80.534; 62.981		620.58Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126309 CIFC11 H14 N2 O2P n a 218.7406; 13.897; 9.5194
90; 90; 90		1156.3Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126310 CIFC11 H13 F3 N2 O3P 1 21/n 114.405; 6.5909; 14.669
90; 105.691; 90		1340.8Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126311 CIFC11 H11 N3 O2P 1 21/c 19.8467; 11.576; 9.697
90; 90.927; 90		1105.17Deka, Jugal Kishore Rai; Sahariah, Biswajit; Baruah, Kalpita; Bar, Arun Kumar; Sarma, Bani Kanta
Conformational control of N-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution.
Chemical communications (Cambridge, England), 2020, 56, 4874-4877
7126312 CIFC22 H16 N6P 1 21/n 17.9437; 10.9876; 10.2274
90; 90.435; 90		892.64Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126313 CIFC26 H16 Cl4 N4 O2 Zn2C 1 2/c 119.5229; 18.0694; 8.8084
90; 102.32; 90		3035.76Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126314 CIFC12 H12 Cl2 Co N4P 1 21/c 110.6519; 8.1804; 15.5453
90; 97.892; 90		1341.7Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126315 CIFC11 H8 Cl2 N2 O ZnP -18.2052; 8.6043; 9.7408
98.959; 97.49; 115.238		599.38Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126316 CIFC68 H76 Cl8 N16 S6 Sn4 Zn4P 42 21 223.7332; 23.7332; 11.4025
90; 90; 90		6422.6Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126317 CIFC68 H77 N16 O S6 Sn4P 1 2/c 115.6802; 20.3433; 12.4505
90; 109.194; 90		3750.77Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126318 CIFC35 H44 Cl4 N8 O2 Ru2 S2P -18.2648; 10.0946; 12.9476
104.143; 101.316; 100.545		996.4Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126319 CIFC79.5 H83 Cl7 N16 S6 Sn4P n a 2125.9881; 22.3278; 15.5336
90; 90; 90		9013.5Geringer, Eugenie; Leusmann, Eliza; Tambornino, Frank; Gerhard, Marina; Koch, Martin; Dehnen, Stefanie
Trapping of ZnCl<sub>2</sub> by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties.
Chemical communications (Cambridge, England), 2020, 56, 4769-4772
7126320 CIFC93 H95 B F24 N4 O3P 1 21/c 118.9774; 14.0644; 34.0542
90; 91.842; 90		9084.6Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126321 CIFC94.5 H99 B Cl2 F24 N4 O3.5P 1 21/n 116.4668; 21.1135; 27.6864
90; 103.746; 90		9350.1Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126322 CIFC66 H100 N4P 1 21/c 118.6997; 17.6316; 20.1905
90; 117.532; 90		5903Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126323 CIFC61 H82 N4 O3P 1 21 122.6094; 17.959; 29.4427
90; 111.156; 90		11149.2Hsueh, Fang-Che; Tsai, Chi-You; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
Interlocking increases the persistence of N-heterocyclic carbenes in solution.
Chemical communications (Cambridge, England), 2020, 56, 4773-4776
7126324 CIFC21 H30 PtP 21 21 215.5867; 10.71; 28.421
90; 90; 90		1700.5Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126325 CIFC74 H63 Au B Cl6 F24 P PtP 112.7747; 12.7853; 13.1193
82.101; 88.764; 64.259		1910.06Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126326 CIFC71 H57 Au B F24 P PtP -112.3657; 15.5627; 19.1346
95.961; 108.064; 101.326		3378.6Ernst, Lukas D.; Koessler, Konstantin; Peter, Andreas; Kratzert, Daniel; Scherer, Harald; Butschke, Burkhard
A heterodinuclear, formal Au<sup>+I</sup>Pt<sup>0</sup> complex with weakly bound alkene ligands.
Chemical communications (Cambridge, England), 2020, 56, 5350-5353
7126327 CIFC17 H9 Cl O3P -18.2844; 8.6986; 10.7524
68.114; 78.9; 68.561		667.83Han, Xi; Kong, Lingheng; Feng, Jiami; Li, Xingwei
Rhodium(iii)-catalyzed synthesis of spirocyclic isoindole N-oxides and isobenzofuranones via C-H activation and spiroannulation.
Chemical communications (Cambridge, England), 2020, 56, 5528-5531
7126328 CIFC H N O SP 114.2587; 18.3783; 25.4318
70.965; 78.342; 79.57		6122.15Wang, Danbo; Kan, Xiaonan; Wu, Chenyu; Gong, Yuzhen; Guo, Guangming; Liang, Tongling; Wang, Lan; Li, Zhibo; Zhao, Yingjie
Charge transfer co-crystals based on donor-acceptor interactions for near-infrared photothermal conversion.
Chemical communications (Cambridge, England), 2020, 56, 5223-5226
7126329 CIFC21 H24 N2 O2 SP -16.9644; 11.4537; 11.8747
97.514; 97.294; 93.446		928.65Molina, Alba; Díaz-Tendero, Sergio; Adrio, Javier; Carretero, Juan C.
Catalytic asymmetric synthesis of diazabicyclo[3.1.0]hexanes by 1,3-dipolar cycloaddition of azomethine ylides with azirines.
Chemical communications (Cambridge, England), 2020, 56, 5050-5053
7126330 CIFC36 H30 N2 O2P -18.9247; 9.9994; 17.016
90.709; 96.541; 116.439		1347.46Molina, Alba; Díaz-Tendero, Sergio; Adrio, Javier; Carretero, Juan C.
Catalytic asymmetric synthesis of diazabicyclo[3.1.0]hexanes by 1,3-dipolar cycloaddition of azomethine ylides with azirines.
Chemical communications (Cambridge, England), 2020, 56, 5050-5053
7126331 CIFC88 H78 N4 P4 Pt2 Si2P -112.9341; 15.4591; 20.0358
70.853; 79.029; 88.937		3711.2Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126332 CIFC85 H75 N4 Ni2 P4 Si2P -112.6509; 16.9249; 17.6665
81.189; 77.4286; 73.2272		3518.3Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126333 CIFC88 H78 N4 P4 Pd2 Si2P -113.545; 17.6245; 17.7005
99.727; 103.685; 109.549		3724.1Frogley, Benjamin J.; Hill, Anthony F.; Sharma, Manab; Sinha, Arup; Ward, Jas S.
Semi-bridging σ-silyls as Z-type ligands.
Chemical communications (Cambridge, England), 2020, 56, 3532-3535
7126334 CIFC134 H136 Cu4 N8 O30P 1 2/n 115.2966; 17.7385; 24.6648
90; 95.051; 90		6666.5Craig, Gavin A.; Larpent, Patrick; Urabe, Hinano; Legrand, Alexandre; Bonneau, Mickaele; Kusaka, Shinpei; Furukawa, Shuhei
Hysteresis in the gas sorption isotherms of metal-organic cages accompanied by subtle changes in molecular packing.
Chemical communications (Cambridge, England), 2020, 56, 3689-3692
7126335 CIFC128.5 H124 Cu4 N7 O29P 1 21/n 114.2345; 29.3603; 16.598
90; 111.254; 90		6465Craig, Gavin A.; Larpent, Patrick; Urabe, Hinano; Legrand, Alexandre; Bonneau, Mickaele; Kusaka, Shinpei; Furukawa, Shuhei
Hysteresis in the gas sorption isotherms of metal-organic cages accompanied by subtle changes in molecular packing.
Chemical communications (Cambridge, England), 2020, 56, 3689-3692
7126336 CIFC51 H60 Cl2 N8P 1 21/c 121.9296; 9.847; 22.4505
90; 109.159; 90		4579.5Zhang, Li-Peng; Li, Xianqiang; Liu, Tianlong; Kang, Lin; Huang, Xing; Zhao, Yuxia
A water-soluble pyrazino[2,3-g]quinoxaline photosensitizer for high-efficiency one- and two-photon excited bioimaging and photodynamic therapy.
Chemical communications (Cambridge, England), 2020, 56, 5544-5547
7126337 CIFC20 H22 N2 O2P 1 21/c 118.7868; 9.84896; 19.3586
90; 108.143; 90		3403.85An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126338 CIFC19 H19 Cl N2 O3P 1 21/n 19.3251; 18.1174; 10.1704
90; 98.755; 90		1698.23An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126339 CIFC20 H22 N2 O3P -19.411; 9.7287; 9.9501
87.849; 85.541; 72.201		864.68An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126340 CIFC17 H16 F N O2P 1 21/n 117.1703; 9.1104; 19.1959
90; 115.406; 90		2712.38An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126341 CIFC17 H16 N2 OP 1 21/n 111.9106; 6.1532; 37.0164
90; 97.119; 90		2692An, Yang; Zhang, Bo-Sheng; Zhang, Zhe; Liu, Ce; Gou, Xue-Ya; Ding, Ya-Nan; Liang, Yong-Min
A carboxylate-assisted amination/unactivated C(sp<sup>2</sup>)-H arylation reaction via a palladium/norbornene cooperative catalysis.
Chemical communications (Cambridge, England), 2020, 56, 5933-5936
7126342 CIFC19 H17 Cu F6 N5 O4P 1 21/n 110.8947; 17.8622; 11.5657
90; 106.714; 90		2155.6Fukatsu, Arisa; Morimoto, Yuma; Sugimoto, Hideki; Itoh, Shinobu
Modelling a 'histidine brace' motif in mononuclear copper monooxygenases.
Chemical communications (Cambridge, England), 2020, 56, 5123-5126
7126343 CIFC25 H36.5 Br4 Fe2 N10.5 O0.5P 1 21/m 113.0724; 19.3867; 13.9064
90; 95.742; 90		3506.6Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126344 CIFC29 H23 Au Cl2 N3 PP 1 21/n 111.3683; 9.5614; 24.806
90; 93.908; 90		2690.1Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126345 CIFC12 H11 Au Cl N3P 1 21/n 113.575; 7.1746; 13.838
90; 106.575; 90		1291.8Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126346 CIFC2.095 H1.905 B0.19 F0.762 N0.571C 1 2/c 127.272; 6.921; 14.9043
90; 116.111; 90		2526.1Chen, Bai-Ling; Zhang, Yuan; Lei, Ya-Ru; Wang, Hui-Ming; Chen, Zili
An allenylidene Au(i) catalyst derived from triazole units and its initial application.
Chemical communications (Cambridge, England), 2020, 56, 5787-5790
7126347 CIFC88 H94 B6 F6 O12C 1 2/c 118.066; 19.955; 24.133
90; 108.477; 90		8251.6Takata, Hisatsugu; Ono, Kosuke; Iwasawa, Nobuharu
Controlled release of the guest molecule via borate formation of a fluorinated boronic ester cage.
Chemical communications (Cambridge, England), 2020, 56, 5613-5616
7126348 CIFC20 H23 N3P 1 21/c 120.236; 9.7971; 17.139
90; 93.473; 90		3391.6Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126349 CIFC24 H25 N3P 1 21/n 111.3125; 9.7429; 17.745
90; 95.103; 90		1948Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126350 CIFC20 H27 N3 OP 1 21/n 118.2435; 11.4952; 18.5875
90; 110.086; 90		3660.9Sathish Kumar, B.; Pati, Narendra N.; Jose, K. V. Jovan; Panda, Pradeepta K.
Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry.
Chemical communications (Cambridge, England), 2020, 56, 5637-5640
7126351 CIFC21 H14 Br2 N2C 1 2/c 128.82; 13.989; 18.95
90; 103.355; 90		7433Zhu, Zhongzhi; Lin, Hanze; Liang, Baihui; Huang, Junjie; Liang, Wanyi; Chen, Lu; Huang, Yubing; Chen, Xiuwen; Li, Yibiao
Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: access to polyaryl 2H-imidazoles.
Chemical communications (Cambridge, England), 2020, 56, 5621-5624
7126352 CIFC48 H65 N O2P 1 21/n 112.1364; 17.5731; 22.0778
90; 92.7639; 90		4703.15Xue, Guodong; Hu, Xiaoguang; Chen, Hanjiao; Ge, Lingbing; Wang, Wenxiang; Xiong, Jingyuan; Miao, Fang; Zheng, Yonghao
Understanding the nature of quinoidal and zwitterionic states in carbazole-based diradicals.
Chemical communications (Cambridge, England), 2020, 56, 5143-5146
7126353 CIFC21 H13 Cl N3 SP b c a15.1373; 14.4119; 16.4702
90; 90; 90		3593.1Guo, Tao; Wei, Xu-Ning; Zhang, Miao; Liu, Yu; Zhu, Li-Min; Zhao, Yun-Hui
Catalyst and additive-free oxidative dual C-H sulfenylation of imidazoheterocycles with elemental sulfur using DMSO as a solvent and an oxidant.
Chemical communications (Cambridge, England), 2020, 56, 5751-5754
7126354 CIFC20 H17 N3 SP 21 21 218.0283; 10.563; 19.1653
90; 90; 90		1625.27Guo, Tao; Wei, Xu-Ning; Zhang, Miao; Liu, Yu; Zhu, Li-Min; Zhao, Yun-Hui
Catalyst and additive-free oxidative dual C-H sulfenylation of imidazoheterocycles with elemental sulfur using DMSO as a solvent and an oxidant.
Chemical communications (Cambridge, England), 2020, 56, 5751-5754
7126355 CIFC27 H30 N2 O3 S2P 1 21/c 113.557; 15.9431; 12.6454
90; 101.401; 90		2679.3Reddy, Angula Chandra Shekar; Ramachandran, Kuppan; Reddy, Palagulla Maheswar; Anbarasan, Pazhamalai
Rhodium-catalyzed Sommelet-Hauser type rearrangement of α-diazoimines: synthesis of functionalized enamides.
Chemical communications (Cambridge, England), 2020, 56, 5649-5652
7126356 CIFC12 H8 N2 S2P b c a6.0865; 17.576; 20.351
90; 90; 90		2177.1Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126357 CIFC18 H12 N2 S2I 1 2 17.8212; 5.9264; 16.1736
90; 91.155; 90		749.52Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126358 CIFC10 H7 N O2 SP 1 21/c 16.9853; 8.3741; 14.638
90; 99.28; 90		845.1Huang, Guoling; Li, Jian; Ji, Xiaoliang; Chen, Lu; Liu, Qiang; Chen, Xiuwen; Huang, Yubing; Li, Yibiao
Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation.
Chemical communications (Cambridge, England), 2020, 56, 5763-5766
7126359 CIFC12 H12 B2 F4 N4 OP 1 21 110.2475; 4.8212; 15.131
90; 109.221; 90		705.88Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126360 CIFC12 H11 B2 F4 N3 O2P n a 2123.933; 12.5943; 4.744
90; 90; 90		1429.93Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126361 CIFC9 H11 B2 F4 N3 OP 1 21/c 112.9329; 4.8706; 19.777
90; 103.631; 90		1210.68Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126362 CIFC14 H16 B2 F4 N4 OP -18.1042; 9.7049; 10.4691
80.218; 86.082; 87.104		808.9Pookkandam Parambil, Shandev; de Jong, Flip; Veys, Koen; Huang, Jianjun; Veettil, Santhini Pulikkal; Verhaeghe, Davy; Van Meervelt, Luc; Escudero, Daniel; Van der Auweraer, Mark; Dehaen, Wim
BOPAHY: a doubly chelated highly fluorescent pyrrole-acyl hydrazone -BF<sub>2</sub> chromophore.
Chemical communications (Cambridge, England), 2020, 56, 5791-5794
7126363 CIFC60.63 H55.12 B2 N5P -116.155; 17.629; 18.2
76.749; 76.424; 74.29		4773.6Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126364 CIFC45 H53 B2 N5P -110.776; 12.867; 15.077
99.007; 108.967; 90.735		1948.1Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126365 CIFC52 H58 B2 F3 N4.87P -110.5695; 15.3466; 16.2221
65.195; 87.805; 72.0887		2260.22Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126366 CIFC53 H64 B2 N6P -113.097; 14.799; 14.975
63.842; 85.29; 64.034		2320Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126367 CIFC47 H58 B2 N4P -18.538; 11.12; 21.468
98.92; 91.29; 96.808		1997.6Prieschl, Dominic; Arrowsmith, Merle; Dietz, Maximilian; Rempel, Anna; Müller, Marcel; Braunschweig, Holger
Synthesis of polyheterocyclic 1,1-diboryltriazenes by γ-nitrogen insertion of azides into activated B-B single bonds.
Chemical communications (Cambridge, England), 2020, 56, 5681-5684
7126368 CIFC50 H60 Au6 F12 N8 O2 P2 S4F d d d :212.36; 29.522; 35.0152
90; 90; 90		12777Salorinne, Kirsi; Man, Renee W. Y.; Lummis, Paul A.; Hazer, Maryam Sabooni Asre; Malola, Sami; Yim, Jacky C.-H.; Veinot, Alex J.; Zhou, Wenxia; Häkkinen, Hannu; Nambo, Masakazu; Crudden, Cathleen M.
Synthesis and properties of an Au<sub>6</sub> cluster supported by a mixed N-heterocyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2020, 56, 6102-6105
7126369 CIFC14 H18 Au Br N2 O SP -19.2685; 9.2937; 10.4915
66.938; 78.837; 79.362		809.82Salorinne, Kirsi; Man, Renee W. Y.; Lummis, Paul A.; Hazer, Maryam Sabooni Asre; Malola, Sami; Yim, Jacky C.-H.; Veinot, Alex J.; Zhou, Wenxia; Häkkinen, Hannu; Nambo, Masakazu; Crudden, Cathleen M.
Synthesis and properties of an Au<sub>6</sub> cluster supported by a mixed N-heterocyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2020, 56, 6102-6105
7126370 CIFC20 H23 B O2C 1 2/c 125.557; 5.612; 25.398
90; 113.817; 90		3333Maza, Ricardo J.; Royes, Jordi; Carbó, Jorge J; Fernández, Elena
Consecutive borylcupration/C-C coupling of γ-alkenyl aldehydes towards diastereoselective 2-(borylmethyl)cycloalkanols.
Chemical communications (Cambridge, England), 2020, 56, 5973-5976
7126371 CIFC26 H35 B O3P 1 21/c 117.9052; 6.4987; 19.8249
90; 100.138; 90		2270.8Maza, Ricardo J.; Royes, Jordi; Carbó, Jorge J; Fernández, Elena
Consecutive borylcupration/C-C coupling of γ-alkenyl aldehydes towards diastereoselective 2-(borylmethyl)cycloalkanols.
Chemical communications (Cambridge, England), 2020, 56, 5973-5976
7126372 CIFC169 H128 Ce20 Cl16 N3 O62P 1 21 120.314; 24.463; 28.508
90; 91.975; 90		14158Russell-Webster, Bradley; Abboud, Khalil A.; Christou, George
Molecular nanoparticles of cerium dioxide: structure-directing effect of halide ions.
Chemical communications (Cambridge, England), 2020, 56, 5382-5385
7126373 CIFC48 H38 Ce3 F0.5 N1.5 O15.5P -114.683; 14.726; 14.909
60.518; 65.035; 62.487		2408Russell-Webster, Bradley; Abboud, Khalil A.; Christou, George
Molecular nanoparticles of cerium dioxide: structure-directing effect of halide ions.
Chemical communications (Cambridge, England), 2020, 56, 5382-5385
7126374 CIFC21 H23 N3 O5P -16.9699; 10.2021; 14.9823
72.265; 77.347; 82.211		987.37Bashir, Muhammad Adnan; Zuo, Honghua; Lu, Xunbo; Wu, Yuzhou; Zhong, Fangrui
Harnessing structurally unbiased ortho-benzoquinone monoimine for biomimetic oxidative [4+2] cycloaddition with enamines.
Chemical communications (Cambridge, England), 2020, 56, 5965-5968
7126375 CIFC89 H70 Cl8 F6 N8 Ni4 O6 PP -114.2332; 16.4798; 19.285
112.704; 92.701; 103.281		4014.6Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126376 CIFC41 H30 N4 Ni2 O3P -113.084; 15.98; 22.737
107.838; 105.17; 95.623		4285Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126377 CIFC71.5 H30 B Cl3 F20 N4 Ni2 O3P -117.673; 19; 19.53
87.662; 78.355; 89.016		6417Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126378 CIFC184 H72 B4 Cl12 F80 N8 Ni4 O6P 1 2/n 117.902; 28.102; 19.0679
90; 90.382; 90		9592.5Jacob, Samuel I.; Douair, Iskander; Wu, Guang; Maron, Laurent; Ménard, Gabriel
A tetranuclear nickel cluster isolated in multiple high-valent states.
Chemical communications (Cambridge, England), 2020, 56, 8182-8185
7126379 CIFC20 H18 N2 O5P -110.0493; 12.6674; 14.606
79.358; 80.034; 89.938		1798.9O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126380 CIFC64 H44 F8 N4 O14P 1 21/c 127.197; 3.7093; 26.924
90; 94.626; 90		2707.3O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126381 CIFC19 H13 F2 N O3P 1 21/c 13.8999; 34.7661; 11.4896
90; 94.404; 90		1553.21O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126382 CIFC36 H24 F4 N2 O6P 1 21/n 13.7762; 29.2094; 13.5261
90; 96.309; 90		1482.9O'Malley, Ciarán; Erxleben, Andrea; Kellehan, Seamus; McArdle, Patrick
Unprecedented morphology control of gas phase cocrystal growth using multi zone heating and tailor made additives.
Chemical communications (Cambridge, England), 2020, 56, 5657-5660
7126383 CIFC108 H123 Al4 Cl3 Dy2 F72 N2 O8P 1 21/c 113.8684; 30.4814; 16.1283
90; 97.72; 90		6756.1Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126384 CIFC26 H44 Li O YP 1 21/n 19.253; 15.4572; 18.3771
90; 94.016; 90		2621.9Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126385 CIFC108 H123 Al4 Cl3 Dy0.2 F72 N2 O8 Y1.8P 1 21/c 114.14639; 30.4739; 16.04187
90; 98.2178; 90		6844.57Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126386 CIFC108 H123 Al4 Cl3 F72 N2 O8 Y2P 1 21/c 114.1215; 30.3026; 16.0232
90; 98.421; 90		6782.7Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126387 CIFC76 H116 Al2 Y2P -111.2354; 12.454; 14.8193
103.894; 100.299; 111.86		1783.5Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126388 CIFC76 H116 Al2 Dy2P -111.1938; 12.4457; 14.8073
104.043; 100.205; 111.785		1774.66Evans, Peter; Reta, Daniel; Goodwin, Conrad A. P.; Ortu, Fabrizio; Chilton, Nicholas F.; Mills, David P.
A double-dysprosocenium single-molecule magnet bound together with neutral ligands.
Chemical communications (Cambridge, England), 2020, 56, 5677-5680
7126389 CIFC101 H104 Al B Dy2 F36 O4P 1 21/c 115.5064; 21.8874; 31.229
90; 101.817; 90		10374.3Errulat, Dylan; Gabidullin, Bulat; Mansikkamäki, Akseli; Murugesu, Muralee
Two heads are better than one: improving magnetic relaxation in the dysprosium metallocene upon dimerization by use of an exceptionally weakly-coordinating anion.
Chemical communications (Cambridge, England), 2020, 56, 5937-5940
7126390 CIFC27.5 H31 B Cl F8 N2 P S2P 1 21/c 115.04; 13.437; 16.768
90; 111.168; 90		3160Adachi, Yohei; Arai, Fuka; Jäkle, Frieder
Extended conjugated borenium dimers via late stage functionalization of air-stable borepinium ions.
Chemical communications (Cambridge, England), 2020, 56, 5119-5122
7126391 CIFC20 H20 N2 O3C 1 2/c 111.906; 21.361; 13.77
90; 105.875; 90		3368Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126392 CIFC20 H20 N2 O3P -18.842; 13.473; 14.699
83.102; 79.47; 89.425		1709Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126393 CIFC63 H60 N2 O8 P2C 1 2/c 133.89; 9.68; 18.339
90; 115.521; 90		5429Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126394 CIFC13 H15 N O2 SP 1 21/c 115.037; 5.654; 16.695
90; 116.037; 90		1275.3Babu, Kaki Raveendra; Han, Wendan; Chen, Jian-Bo; Li, Yang; Tang, Yuhai; Zhang, Wenquan; Xu, Wenbo; Xu, Silong
A three-component reaction of phosphorus ylides with isocyanates: facile synthesis of 2-amino-3-carboxylate-4-quinolones.
Chemical communications (Cambridge, England), 2020, 56, 5909-5912
7126395 CIFC66 H82 B Br Mo N6 O5 P2 PtP 1 21/n 122.4595; 12.1952; 24.7641
90; 102.513; 90		6621.73Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126396 CIFC76 H82 B2 Br2 Cl8 Mo2 N12 O4 P2 Pd2P 1 21/n 111.3977; 30.1539; 13.2985
90; 109.428; 90		4310.25Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126397 CIFC54 H52 B Br N6 O2 P2 Pt WP 1 21/n 19.5923; 22.6404; 23.4154
90; 98.636; 90		5027.55Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126398 CIFC44 H46 B Br Mo N6 O2 P2 PdC 1 2/c 142.971; 10.446; 20.5602
90; 94.607; 90		9199.1Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126399 CIFC82 H92 B2 Br2 Mo2 N12 O7 P2 Pd2P 1 21/n 127.0575; 11.7128; 29.6534
90; 104.965; 90		9079Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126400 CIFC82 H99 B2 Br2 Mo2 N12 O6.5 P2 Pt2P 1 21/n 126.9732; 11.6694; 29.657
90; 105.134; 90		9011.1Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126401 CIFC39 H40 B Br Cl9 N6 O2 P Pd WP -111.41; 13.4275; 17.2454
85.274; 87.055; 70.772		2485.43Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126402 CIFC52 H52 B Br N6 O2 P2 Pd WP 1 21/n 121.7995; 12.8236; 22.874
90; 111.409; 90		5953.2Burt, Liam K.; Cordiner, Richard L.; Hill, Anthony F.; Manzano, Richard A.; Wagler, Jörg
The significance of phosphoniocarbynes in halocarbyne cross-coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 5673-5676
7126403 CIFC48 H58 Au N3P 1 21/n 110.797; 16.6498; 24.697
90; 95.768; 90		4417.2Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126404 CIFC34 H34 Cl2 I NP n a 2118.2744; 10.4465; 17.007
90; 90; 90		3246.7Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126405 CIFC41 H45 Cl3 N2 PdP 1 21/n 18.822; 20.173; 21.011
90; 93.993; 90		3730.2Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126406 CIFC63 H78 Au B2 F8 N5 PdP 1 21/m 115.3922; 14.4465; 16.7191
90; 115.716; 90		3349.5Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126407 CIFC46 H42 Au F3 N O3 P SP 1 21/c 114.4529; 13.4595; 21.5529
90; 93.956; 90		4182.67Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126408 CIFC59 H70 Au Cl2 F3 N O5 P3 Pd SP -113.9859; 14.735; 15.1208
84.537; 82.442; 89.562		3074.99Wang, Jiwei; Zhan, Licheng; Wang, Gendi; Wei, Yin; Shi, Min; Zhang, Jun
Pd-Promoted cross coupling of iodobenzene with vinylgold via an unprecedented phenyl transmetalation from Pd to Au.
Chemical communications (Cambridge, England), 2020, 56, 6213-6216
7126409 CIFC12 H28 Br12 Cu6 N4 PbR -3 :H11.453; 11.453; 22.637
90; 90; 120		2571.5Jing, Chang-Qing; Wu, Jia-Hang; Cao, Yao-Yao; Che, Hang-Xin; Zhao, Xian-Mei; Yue, Meng; Liao, Yuan-Yuan; Yue, Cheng-Yang; Lei, Xiao-Wu
A three-dimensional cuprous lead bromide framework with highly efficient and stable thermochromic luminescence properties.
Chemical communications (Cambridge, England), 2020, 56, 5925-5928
7126410 CIFC13 H14 N2 O2I 1 2/a 116.722; 7.3514; 20.934
90; 102.85; 90		2509Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126411 CIFC8 H8 N4P 1 21/n 19.7747; 5.6834; 14.3307
90; 96.261; 90		791.37Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126412 CIFC14 H16 N2 O2P 1 21/n 18.1279; 8.6652; 18.746
90; 96.939; 90		1310.6Wang, Ya; Zhou, Yao; Song, Qiuling
[3+1+1] type cyclization of ClCF<sub>2</sub>COONa for the assembly of imidazoles and tetrazoles via in situ generated isocyanides.
Chemical communications (Cambridge, England), 2020, 56, 6106-6109
7126413 CIFC53 H46 N4P -111.7669; 12.1939; 15.1362
102.506; 97.611; 102.676		2031.3Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126414 CIFC77 H64 N6P 1 21/n 118.369; 16.572; 20.32
90; 99.726; 90		6096.7Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126415 CIFC93 H96 N6P -112.351; 18.25; 19.587
101.343; 93.315; 108.024		4082.9Li, Kuofei; Zhu, Yunhui; Yao, Bing; Chen, Yuannan; Deng, Hao; Zhang, Qisheng; Zhan, Hongmei; Xie, Zhiyuan; Cheng, Yanxiang
Rotation-restricted thermally activated delayed fluorescence compounds for efficient solution-processed OLEDs with EQEs of up to 24.3% and small roll-off.
Chemical communications (Cambridge, England), 2020, 56, 5957-5960
7126416 CIFC94 H58 N8 O24 Zn3P 1 21 112.652; 18.915; 21.672
90; 105.25; 90		5004Li, Peng; Sui, Qi; Guo, Meng-Yue; Yang, Shuai-Liang; Bu, Ran; Gao, En-Qing
Selective chemochromic and chemically-induced photochromic response of a metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 5929-5932
7126417 CIFC18 H20 N2 O4P 21 21 2111.5787; 16.5844; 17.9315
90; 90; 90		3443.3Velázquez, Marta; Alberca, Saúl; Iglesias-Sigüenza, Javier; Fernández, Rosario; Lassaletta, José M; Monge, David
Catalytic enantioselective synthesis of α-aryl α-hydrazino esters and amides.
Chemical communications (Cambridge, England), 2020, 56, 5823-5826
7126418 CIFC28 H38 Cl6 N2 PdP 1 21/n 112.8037; 17.1488; 15.3764
90; 104.478; 90		3268.95Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126419 CIFC23 H20 Cl2 N P PdP 1 21/c 18.8655; 10.7674; 22.2732
90; 93.155; 90		2122.94Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126420 CIFC20.5 H29.5 Cl3.5 N3 PdP c c 226.6806; 15.682; 11.6312
90; 90; 90		4866.55Guillet, Sébastien G; Voloshkin, Vladislav A.; Saab, Marina; Beliš, Marek; Van Hecke, Kristof; Nahra, Fady; Nolan, Steven P.
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR<sub>3</sub> pre-catalysts.
Chemical communications (Cambridge, England), 2020, 56, 5953-5956
7126421 CIFC14 H13 N O4P -17.1411; 7.8726; 10.6572
102.1; 92.658; 101.463		571.71Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126422 CIFC16 H20 N O5 PP 1 21/c 113.804; 13.802; 16.169
90; 90.79; 90		3080.3Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126423 CIFC32 H31 Cl3 Eu F9 N2 O21 S3C 1 2/c 127.777; 14.271; 26.502
90; 115.444; 90		9487Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126424 CIFC35 H50 Eu F9 N2 O24 P2 S3P 1 21/n 115.919; 13.486; 24.95
90; 105.115; 90		5171Fueyo-González, Francisco; Garcia-Fernandez, Emilio; Martínez, David; Infantes, Lourdes; Orte, Angel; González-Vera, Juan A; Herranz, Rosario
Smart lanthanide antennas for sensing water.
Chemical communications (Cambridge, England), 2020, 56, 5484-5487
7126425 CIFC39 H38 B F2 N3 O5P -111.152; 12.967; 13.78
113.934; 105.531; 98.396		1679.9Ou, Changjin; Zhang, Yewei; Ge, Wei; Zhong, Liping; Huang, Yong; Si, Weili; Wang, Wenjun; Zhao, Yongxiang; Dong, Xiaochen
A three-dimensional BODIPY-iron(iii) compound with improved H<sub>2</sub>O<sub>2</sub>-response for NIR-II photoacoustic imaging guided chemodynamic/photothermal therapy.
Chemical communications (Cambridge, England), 2020, 56, 6281-6284
7126426 CIFC64 H54 Fe3 N12 O2P 1 21/n 111.719; 22.281; 20.337
90; 91.485; 90		5308Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126427 CIFC64 H54.36 N12 O2.18 Zn3P 1 21/n 111.5922; 22.523; 20.5743
90; 92.1491; 90		5368Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126428 CIFC64 H54 Fe2 N12 O2 ZnP 1 21/n 111.664; 22.4568; 20.4213
90; 91.781; 90		5346.5Hyun, Sung-Min; Upadhyay, Apoorva; Das, Anuvab; Burns, Corey P.; Sung, Siyoung; Beaty, Jeremy D.; Bhuvanesh, Nattamai; Nippe, Michael; Powers, David C.
Kinetic versus thermodynamic metalation enables synthesis of isostructural homo- and heterometallic trinuclear clusters.
Chemical communications (Cambridge, England), 2020, 56, 5893-5896
7126429 CIFC19.99 H28.37 K1.15 Mn3.25 Na O15.73C 1 2/c 124.928; 24.515; 25.527
90; 112.915; 90		14369Liu, Shuai; Deng, Youmei; Xu, Feng
An inorganic-organic hybrid Mn<sup>III</sup>{Mn}<sub>2</sub> cluster consisting of rare Lindqvist-like Mn<sub>6</sub> subunits with high proton conductivity.
Chemical communications (Cambridge, England), 2020, 56, 6066-6069
7126430 CIFC44 H34 OP 1 21/n 18.0514; 29.7733; 12.8449
90; 92.127; 90		3077.02Mori, Sakura; Akita, Motoko; Suzuki, Shuichi; Asano, Motoko S.; Murata, Michihisa; Akiyama, Tsuyoshi; Matsumoto, Taisuke; Kitamura, Chitoshi; Kato, Shin-Ichiro
Open-shell singlet diradicaloid difluoreno[4,3-b:3',4'-d]furan and its radical cation and dianion.
Chemical communications (Cambridge, England), 2020, 56, 5881-5884
7126431 CIFB Ba6 Cl9 O3P 1 21/n 18.229; 12.2589; 19.08
90; 90.203; 90		1924.7Li, Wei; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>6</sub>BO<sub>3</sub>Cl<sub>9</sub> and Pb<sub>6</sub>BO<sub>4</sub>Cl<sub>7</sub>: structural insights into ortho-borates with uncondensed BO<sub>4</sub> tetrahedra.
Chemical communications (Cambridge, England), 2020, 56, 6086-6089
7126432 CIFB Cl7 O4 Pb6P -18.001; 8.054; 13.116
89.522; 89.663; 69.942		793.9Li, Wei; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>6</sub>BO<sub>3</sub>Cl<sub>9</sub> and Pb<sub>6</sub>BO<sub>4</sub>Cl<sub>7</sub>: structural insights into ortho-borates with uncondensed BO<sub>4</sub> tetrahedra.
Chemical communications (Cambridge, England), 2020, 56, 6086-6089
7126433 CIFC24 H29 B F2 O3P -110.1095; 14.6951; 16.0516
70.598; 79.739; 77.184		2178.99Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126434 CIFC24 H29 B F2 O3P -18.4132; 9.9177; 15.6851
74.475; 86.897; 66.845		1157.49Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126435 CIFC24 H29 B F2 O3P -18.5049; 9.9575; 15.6872
74.405; 86.917; 66.543		1171.72Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126436 CIFC24 H29 B F2 O3P -110.1447; 15.1024; 16.1256
70.107; 78.921; 78.57		2256.1Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126437 CIFC17 H15 B F2 O3P 1 21/c 17.6754; 19.1327; 10.149
90; 102.782; 90		1453.46Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126438 CIFC24 H29 B F2 O3P -110.1293; 14.9169; 16.0997
70.326; 79.384; 77.847		2222.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126439 CIFC24 H29 B F2 O3P -110.1217; 14.766; 16.0705
70.555; 79.713; 77.319		2195.03Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126440 CIFC24 H29 B F2 O3P -110.1611; 15.2065; 16.1543
70.258; 78.911; 79.039		2284.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126441 CIFC20 H21 B F2 O3P b c a7.1609; 10.0337; 48.7164
90; 90; 90		3500.29Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126442 CIFC17 H15 B F2 O3P 1 21/c 17.9445; 19.2382; 10.3606
90; 104.183; 90		1535.2Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126443 CIFC17 H15 B F2 O3P 1 21/c 17.8494; 19.191; 10.3146
90; 103.76; 90		1509.18Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126444 CIFC17 H15 B F2 O3P 1 21/c 17.7481; 19.1442; 10.2334
90; 103.133; 90		1478.23Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126445 CIFC20 H21 B F2 O3P b c a7.1936; 10.205; 50.76
90; 90; 90		3726Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126446 CIFC20 H21 B F2 O3P b c a7.2099; 10.1738; 49.415
90; 90; 90		3624.7Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126447 CIFC20 H21 B F2 O3P b c a7.175; 10.0917; 49.0041
90; 90; 90		3548.29Wang, Jian-Xin; Yu, Yi-Shuai; Niu, Li-Ya; Zou, Bo; Wang, Kai; Yang, Qing-Zheng
A difluoroboron β-diketonate based thermometer with temperature-dependent emission wavelength.
Chemical communications (Cambridge, England), 2020, 56, 6269-6272
7126448 CIFC31 H38 N4 O5P 21 21 2110.1246; 16.0039; 18.3736
90; 90; 90		2977.13Wang, Donglei; Jiang, Qianwen; Yang, Xiaoyu
Atroposelective synthesis of configurationally stable nonbiaryl N-C atropisomers through direct asymmetric aminations of 1,3-benzenediamines.
Chemical communications (Cambridge, England), 2020, 56, 6201-6204
7126449 CIFC8 H12 Cl2 Cu N5 O0.5P -17.7357; 12.816; 13.522
110.78; 103.66; 96.17		1190.6Schäfer, Dominic; Fink, Fabian; Kleinschmidt, Denise; Keisers, Kristina; Thomas, Fabian; Hoffmann, Alexander; Pich, Andrij; Herres-Pawlis, Sonja
Enhanced catalytic activity of copper complexes in microgels for aerobic oxidation of benzyl alcohols.
Chemical communications (Cambridge, England), 2020, 56, 5601-5604
7126450 CIFC23 H16 B F10 N SP 1 21 110.5637; 7.3903; 13.8954
90; 98.8924; 90		1071.76Fischer, Malte; Schmidtmann, Marc
B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>- and HB(C<sub>6</sub>F<sub>5</sub>)<sub>2</sub>-mediated transformations of isothiocyanates.
Chemical communications (Cambridge, England), 2020, 56, 6205-6208
7126451 CIFC16 H20 O8 Zn2P n a 2117.8332; 9.0061; 13.2032
90; 90; 90		2120.53Zhang, Jiajia; Cui, Fang; Li, Li; Liu, Yang; Zhang, Xiao; Cui, Tieyu
From coordination polymers to nanocrystals: general and facile synthesis of ultra-small metal oxide nanocrystals.
Chemical communications (Cambridge, England), 2020, 56, 6145-6148
7126452 CIFC14 H5 N3 O5P 1 21/c 15.0814; 6.9825; 17.0804
90; 93.994; 90		604.56Niazi, Muhammad Rizwan; Hamzehpoor, Ehsan; Ghamari, Pegah; Perepichka, Igor F.; Perepichka, Dmitrii F.
Nitroaromatics as n-type organic semiconductors for field effect transistors.
Chemical communications (Cambridge, England), 2020, 56, 6432-6435
7126453 CIFC14 H10 Cu N2 O3P 1 21/n 16.4066; 18.6435; 9.8389
90; 96.696; 90		1167.16Khanra, Somnath; Ta, Sabyasachi; Paladhi, Ankush; Ghosh, Milan; Ghosh, Subhasis; Hira, Sumit Kumar; Manna, Partha Partim; Brandão, Paula; Félix, Vítor; Das, Debasis
A polynuclear Cu(ii) complex for real time monitoring of mitochondrial cytochrome C release during cellular apoptosis.
Chemical communications (Cambridge, England), 2020, 56, 6563-6566
7126454 CIFC52 H48 B F24 N2 Na O7P 1 21/c 112.7633; 18.502; 24.5224
90; 96.5057; 90		5753.6Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126455 CIFC44 H82 Cl0 Cu2 F24 N4 Na2 O15 P4P 1 21/n 110.5906; 25.0689; 12.4435
90; 92.9669; 90		3299.3Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126456 CIFC24 H44 Cu F12 N2 Na O9 P2P -111.243; 12.5262; 14.6345
64.708; 87.283; 73.184		1776.8Iniesta, Ester; Vidal-Ferran, Anton
Supramolecularly regulated copper-bisoxazoline catalysts for the efficient insertion of carbenoid species into hydroxyl bonds.
Chemical communications (Cambridge, England), 2020, 56, 6364-6367
7126457 CIFC15 H14 F3 N O2 SC 1 2/c 125.516; 5.6738; 21.937
90; 110.176; 90		2981Zeng, Hao; Zhu, Chuanle; Liu, Chi; Cai, Yingying; Chen, Fulin; Jiang, Huanfeng
Three component hydroxyletherification and hydroxylazidation of (trifluoromethyl)alkenes: access to α-trifluoromethyl β-heteroatom substituted tertiary alcohols.
Chemical communications (Cambridge, England), 2020, 56, 6241-6244
7126458 CIFC6 H11 F O4P 1 21 18.1522; 4.739; 9.7711
90; 99.908; 90		371.86Valverde, Pablo; Vendeville, Jean-Baptiste; Hollingsworth, Kristian; Mattey, Ashley P.; Keenan, Tessa; Chidwick, Harriet; Ledru, Helene; Huonnic, Kler; Huang, Kun; Light, Mark E.; Turner, Nicholas; Jiménez-Barbero, Jesús; Galan, M. Carmen; Fascione, Martin A.; Flitsch, Sabine; Turnbull, W. Bruce; Linclau, Bruno
Chemoenzymatic synthesis of 3-deoxy-3-fluoro-l-fucose and its enzymatic incorporation into glycoconjugates.
Chemical communications (Cambridge, England), 2020, 56, 6408-6411
7126459 CIFC77 H118 Al2 N6 O2C 1 2/c 123.926; 13.52; 47.134
90; 98.006; 90		15098Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126460 CIFC70 H108 Al2 N8P -111.946; 14.183; 21.699
71.614; 88.934; 76.753		3390.2Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126461 CIFC85.5 H128 Al2 N8P -112.9012; 15.4561; 22.3126
100.431; 95.38; 110.218		4046.7Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126462 CIFC215 H318 Al4 N16 Na2 O4P -113.092; 17.852; 21.332
90.53; 90.05; 96.922		4949Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126463 CIFC37 H59 Al N4P 4112.7376; 12.7376; 22.3806
90; 90; 90		3631.2Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126464 CIFC53 H75 Al N4P c a 2120.25; 12.5817; 18.94
90; 90; 90		4825.5Xiao, Lin; Chen, Weixing; Shen, Lingyi; Liu, Li; Xue, Yujie; Zhao, Yanxia; Yang, Xiao-Juan
Reduction of carbodiimides by a dialumane through insertion and cycloaddition.
Chemical communications (Cambridge, England), 2020, 56, 6352-6355
7126465 CIFC17 H13 I O4P -19.5534; 9.6302; 10.2451
74.922; 85.722; 61.931		801.8Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126466 CIFC18 H14 F I O4P 21 21 218.7643; 9.1745; 20.1935
90; 90; 90		1623.72Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126467 CIFC19 H15 I O4P 1 21/n 18.0931; 13.1306; 15.5266
90; 95.488; 90		1642.41Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126468 CIFC19 H17 I O5P -19.8357; 10.4353; 10.4634
111.642; 106.312; 106.245		865.1Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126469 CIFC19 H14 F3 I O4C 1 c 19.2645; 22.2327; 18.2492
90; 101.504; 90		3683.36Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126470 CIFC19 H17 I O4P 1 21/n 110.5655; 14.926; 11.4963
90; 107.437; 90		1729.66Tang, Pan-Ting; Shao, You-Xiang; Wang, Liang-Neng; Wei, Yi; Li, Ming; Zhang, Ni-Juan; Luo, Xiao-Peng; Ke, Zhuofeng; Liu, Yue-Jin; Zeng, Ming-Hua
Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 6680-6683
7126471 CIFC24 H40 Cl2 Cu2 N2 O3 P2P n a 2117.8896; 11.8315; 14.1427
90; 90; 90		2993.46Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126472 CIFC16 H38 Cl2 Ni O2 P2P -17.8506; 8.205; 9.6512
111.818; 100.304; 97.698		554Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126473 CIFC26 H44 Br2 N2 Ni O3.5 P2P -18.2836; 11.8373; 16.2323
93.988; 96.686; 93.178		1573.77Scheerder, Arthur R.; Lutz, Martin; Broere, Daniël L J
Unexpected reactivity of a PONNOP 'expanded pincer' ligand.
Chemical communications (Cambridge, England), 2020, 56, 8198-8201
7126474 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.8059; 5.8059; 13.905
90; 90; 90		468.72Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126475 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.6443; 5.6443; 13.507
90; 90; 90		430.31Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126476 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.7051; 5.7051; 13.6603
90; 90; 90		444.62Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126477 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.6753; 5.6753; 13.593
90; 90; 90		437.82Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126478 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5997; 5.5997; 13.351
90; 90; 90		418.64Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126479 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.758; 5.758; 13.794
90; 90; 90		457.33Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126480 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.7382; 5.7382; 13.747
90; 90; 90		452.65Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126481 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5308; 5.5308; 13.126
90; 90; 90		401.5Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126482 CIFC4 H1.5 D0.5 N2 O4P 41 21 25.5604; 5.5604; 13.245
90; 90; 90		409.51Funnell, Nicholas P.; Bull, Craig L.; Ridley, Christopher J.; Parsons, Simon; Tellam, James P.
Alloxan under pressure-squeezing an extremely dense molecular crystal structure.
Chemical communications (Cambridge, England), 2020, 56, 6428-6431
7126483 CIFC78 H54 Cd3 N4 O14P -116.32; 16.974; 19.292
88.171; 70.164; 62.671		4417Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126484 CIFC89 H73 Cd3 Cl3 N6 O14P -116.4; 16.98; 20.488
92.38; 111.486; 116.958		4581.4Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126485 CIFC81.1 H58.4 Cd3 Cl3 N4.5 O13.7P -116.36; 17.031; 19.943
89.551; 69.596; 62.889		4559Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126486 CIFC69 H49 Cd3 N3 O14P -116.754; 16.894; 18.001
66.663; 77.37; 62.283		4137.7Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126487 CIFC83.5 H62.1 Cd3 N5.1 O13.5P -116.377; 17.024; 20.123
90.241; 110.656; 117.102		4580.7Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126488 CIFC94 H83 Cd3 Cl3 N7 O15P -116.459; 17.028; 20.704
92.164; 111.745; 117.015		4650Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126489 CIFC69.75 H50.75 Cd3 N3.25 O14.25P -116.713; 16.927; 17.944
65.931; 77.105; 62.489		4107.1Chen, Jing; Chao, Meng-Yao; Yan Liu, ?; Xu, Bo-Wei; Zhang, Wen-Hua; Young, David J.
An N,N'-diethylformamide solvent-induced conversion cascade within a metal-organic framework single crystal.
Chemical communications (Cambridge, England), 2020, 56, 5877-5880
7126490 CIFC6 H36 Cl6 Cu12 N6 S6P m -3 m12.3881; 12.3881; 12.3881
90; 90; 90		1901.14Hu, Lanxia; Zheng, Aiping; Kang, Yao; Wen, Tian; Zhang, Jian
A supersalt-type copper(i)-thiolate cluster with applications for mechano/thermochromism and the oxygen evolution reaction.
Chemical communications (Cambridge, England), 2020, 56, 3967-3970
7126491 CIFC128 H96 N16 O16C 1 c 122.05; 10.76; 9.34
90; 101.29; 90		2173.1Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126492 CIFC32 H8 N8 O8 S0P 1 21/c 18.09; 6.39; 11.63
90; 104.71; 90		581.5Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126493 CIFC432 H560 N64 O60 S16P 1 21/n 115.09; 19.55; 34.77
90; 94.63; 90		10224Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126494 CIFC19 H24.04 F3 O6 SP -19.3575; 10.2713; 11.5278
94.471; 104.322; 108.484		1003.31Cheng, Ruixiang; Xiong, Wenfang; Qi, Chaorong; Wang, Lu; Ren, Yanwei; Jiang, Huanfeng
Macrocyclization of 3-triflyloxybenzynes with tetrahydrofuran via an anionic thia-Fries rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 6495-6498
7126495 CIFC4 H2 F3 N3 O4 SP 1 21/c 112.0715; 5.7257; 12.5111
90; 101.199; 90		848.27Zhang, Wei; Lin, Jin-Hong; Zhang, Pengfei; Xiao, Ji-Chang
A convenient reagent for the conversion of aldoximes into nitriles and isonitriles.
Chemical communications (Cambridge, England), 2020, 56, 6221-6224
7126496 CIFC14 H30 Cl4 Fe N4 O4P c a 2112.504; 12.83; 13.185
90; 90; 90		2115.2Hay, Moya A.; Sarkar, Arup; Craig, Gavin A.; Marriott, Katie E. R.; Wilson, Claire; Rajaraman, Gopalan; Murrie, Mark
A large axial magnetic anisotropy in trigonal bipyramidal Fe(ii).
Chemical communications (Cambridge, England), 2020, 56, 6826-6829
7126497 CIFC63 H47 N5 O22P -113.7033; 14.2585; 15.6635
104.701; 100.957; 99.729		2829.3Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126498 CIFC64 H38 N2 O16P -18.8579; 15.7231; 20.017
110.471; 93.635; 106.238		2467Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126499 CIFC64 H42 N2 O16P 1 21/c 18.4167; 28.6453; 20.8697
90; 100.155; 90		4952.8Yelgaonkar, Shweta P.; Kiani, Daniyal; Baltrusaitis, Jonas; MacGillivray, Leonard R.
Superstructural diversity in salt-cocrystals: higher-order hydrogen-bonded assemblies formed using U-shaped dications and with assistance of π<sup>-</sup>-π stacking.
Chemical communications (Cambridge, England), 2020, 56, 6708-6710
7126500 CIFC9.6 H7.2 F0.8 N1.6 O2.4P n a 2113.7895; 20.62; 3.8818
90; 90; 90		1103.7Sasmal, Sheuli; Sinha, Soumya Kumar; Lahiri, Goutam Kumar; Maiti, Debabrata
A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols.
Chemical communications (Cambridge, England), 2020, 56, 7100-7103
7126501 CIFC5.33 H4.44 N0.89 O1.78P 1 21/c 18.531; 11.1285; 12.0481
90; 110.333; 90		1072.54Sasmal, Sheuli; Sinha, Soumya Kumar; Lahiri, Goutam Kumar; Maiti, Debabrata
A directing group-assisted ruthenium-catalyzed approach to access meta-nitrated phenols.
Chemical communications (Cambridge, England), 2020, 56, 7100-7103
7126502 CIFC84 H48 N12 O38 Th6F m -3 m30.4822; 30.4822; 30.4822
90; 90; 90		28323Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126503 CIFC60 H36 O38 Th6F m -3 m25.052; 25.052; 25.052
90; 90; 90		15722.7Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126504 CIFC42 H24 O19 Th3F m -3 m27.9387; 27.9387; 27.9387
90; 90; 90		21808.1Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126505 CIFC24 H12 O19 Th3F m -3 m21.9026; 21.9026; 21.9026
90; 90; 90		10507.2Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126506 CIFC144 H96 O76 Th12F m -3 m28.2063; 28.2063; 28.2063
90; 90; 90		22440.8Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126507 CIFC399.36 H249.6 O155.84 Th24F m -3 m30.976; 30.976; 30.976
90; 90; 90		29722Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126508 CIFC48 H24 O94 Th12F m -3 m19.0604; 19.0604; 19.0604
90; 90; 90		6924.6Li, Zi-Jian; Ju, Yu; Yu, Bowen; Wu, Xiaoling; Lu, Huangjie; Li, Yongxin; Zhou, Jing; Guo, Xiaofeng; Zhang, Zhi-Hui; Lin, Jian; Wang, Jian-Qiang; Wang, Shuao
Modulated synthesis and isoreticular expansion of Th-MOFs with record high pore volume and surface area for iodine adsorption.
Chemical communications (Cambridge, England), 2020, 56, 6715-6718
7126509 CIFC26 H32 La1.11 N4.67 O14.17R 3 2 :H16.2731; 16.2731; 66.968
90; 90; 120		15358.1Wang, Shanshan; Li, Shuning; Xiong, Junyu; Lin, Zhengguo; Wei, Wei; Xu, Yanqing
Near-infrared photothermal conversion of stable radicals photoinduced from a viologen-based coordination polymer.
Chemical communications (Cambridge, England), 2020, 56, 7399-7402
7126510 CIFC25 H22 Cl F3 N4P 1 21 15.6933; 12.7845; 15.7666
90; 99.16; 90		1132.95Stewart, Hannah L.; Hanby, Abigail R.; King, Thomas A.; Bond, Andrew D.; Moss, Thomas A.; Sore, Hannah F.; Spring, David R.
An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 6818-6821

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