Crystallography Open Database

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7119150 CIFC20.45 H30.90 Na O14.46P 1 21 16.6481; 24.625; 14.756
90; 102.798; 90
2355.7Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119151 CIFC20.29 H30.59 Na O14P 1 21 16.6239; 24.772; 14.6783
90; 102.43; 90
2352.1Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119152 CIFC2 H6 CdP 42/m n m7.195; 7.195; 4.118
90; 90; 90
213.2Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119153 CIFC2 H6 CdP 1 21/n 17.483; 7.711; 7.734
90; 115.85; 90
401.6Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119160 CIFC13 H16 N2 O7P 1 21/c 112.554; 8.8499; 12.6253
90; 103.988; 90
1361.1Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119161 CIFC7 H8 O6P 1 21/n 13.6803; 27.724; 9.3579
90; 94.397; 90
952Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119162 CIFC15 H13 N3 O4 SP -17.8557; 10.1043; 10.4713
80.602; 68.952; 69.742
727.01Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119163 CIFC15 H13 N3 O4 SP -112.6899; 14.6928; 20.5097
84.866; 74.669; 84.683
3663.7Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119164 CIFC46 H43 N9 O13 S3P -17.0374; 12.917; 25.467
84.077; 89.174; 83.327
2287Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119165 CIFC16 H15 N OP b c a9.0171; 11.0071; 23.9483
90; 90; 90
2376.9Vijay K. Srirambhatla; Rui Guo; Sarah L. Price; Alastair J. Florence
Isomorphous template induced crystallisation: a robust method for the targeted crystallisation of computationally predicted metastable polymorphs
Chem.Commun., 2016, 52, 7384
7119166 CIFC26 H16 S2P 1 21/n 115.113; 7.708; 16.178
90; 94; 90
1880Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119167 CIFC26 H16 S2C 1 2/c 117.08; 11.919; 19.8
90; 104.04; 90
3910.4Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119168 CIFC22 H23 N3 O4P 1 21/n 110.9129; 7.8194; 22.428
90; 97.304; 90
1898.3Haiyan Yu; Wang Ren; Hongguang Lu; Yanan Liang; Qiusheng Wang
Synthesis and piezochromic luminescence study of a coumarin hydrozone compound
Chem.Commun., 2016, 52, 7387
7119169 CIFC21 H11 F26 N O2P -112.37; 12.834; 18.49
98.783; 91.487; 104.872
2797.3Yohei Haketa; Ryota Takasago; Hiromitsu Maeda
beta-Perfluoroalkyl-substituted pyrrole as an anion-responsive pi-electronic system through a single NH moiety
Chem.Commun., 2016, 52, 7364
7119170 CIFC132 H108 Cd4 N20 O12C 1 2/c 131.093; 34.507; 24.271
90; 128.646; 90
20339Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119171 CIFC70 H56 B Cd2 F4 N10 O8I b a m12.5188; 15.3848; 42.5644
90; 90; 90
8197.9Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119172 CIFC105 H69 Cd3 F9 N15 O24 Re3R 3 c :H18.6042; 18.6042; 51.5285
90; 90; 120
15445.4Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119173 CIFC64 H60 F3 N12 O52 P W12 Zn2P 4/n :219.5965; 19.5965; 16.078
90; 90; 90
6174.32Jian-Zhen Liao; Chen Wu; Xiao-Yuan Wu; Shui-Quan Deng; Can-Zhong Lu
Exceptional photosensitivity of a polyoxometalate-based charge-transfer hybrid material
Chem.Commun., 2016, 52, 7394
7119174 CIFC18 H16 O4P 1 21/c 111.891; 16.2219; 15.2941
90; 93.262; 90
2945.4Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119175 CIFC19 H18 O4P 1 21/n 15.7294; 16.4971; 16.9275
90; 96.391; 90
1590Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119176 CIFMn1.5 N O13 V4P 1 2/m 18.2011; 3.5207; 9.9129
90; 110.987; 90
267.234Martin K. Dufficy; Lan Luo; Peter S. Fedkiw; Paul A. Maggard
Vacancy-induced manganese vanadates and their potential application to Li-ion batteries
Chem.Commun., 2016, 52, 7509
7119177 CIFC12 H8 Co3 K O20I -4 2 d13.0691; 13.0691; 30.157
90; 90; 90
5150.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119178 CIFC12 H8 Co3 K O18I -4 2 d13.0005; 13.0005; 30.2002
90; 90; 90
5104.2Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119179 CIFC12 H8 Co3 K O18I -4 2 d12.8201; 12.8201; 30.2685
90; 90; 90
4974.8Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119180 CIFC12 H8 Co3 K O18I -4 2 d12.6111; 12.6111; 30.2999
90; 90; 90
4818.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119181 CIFC21 H20 O4P 21 21 215.9638; 7.4011; 40.7678
90; 90; 90
1799.44Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119182 CIFC39 H38 N O P SP 21 21 218.966; 10.6824; 34.6972
90; 90; 90
3323.2Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119183 CIFC16 H21 B Fe O2P 1 21/n 112.7414; 7.5452; 15.8499
90; 104.524; 90
1475.06Anis Tlili; Arnaud Voituriez; Angela Marinetti; Pierre Thuery; Thibault Cantat
Synergistic effects in ambiphilic phosphino-borane catalysts for the hydroboration of CO2
Chem.Commun., 2016, 52, 7553
7119350 CIFC6 Cl8 N10 O8P 1 21/c 16.1067; 13.7465; 12.4167
90; 96.024; 90
1036.57Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119351 CIFC4 H2 Cl2 N10 O8P 1 21/c 110.3037; 9.6323; 14.3934
90; 107.927; 90
1359.17Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119352 CIFC47 H43 Ag3 F6 N12 O7 S2P -112.88; 13.13; 15.88
99.38; 90.29; 101.76
2592Hui; Guo; Xin; He; Chong-Qing; Wan; Liang; Zhao
A stepwise bulk-to-cluster-to-particle transformation toward the efficient synthesis of alkynyl-protected silver nanoclusters
Chem.Commun., 2016, 52, 7723
7119353 CIFC24 H27 Br O5P 1 21 111.882; 6.1817; 15.84
90; 108.485; 90
1103.4Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119354 CIFC43 H44 N3 O5 RhP 21 21 2112.6831; 13.3648; 25.5629
90; 90; 90
4333.1Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119355 CIFC24 H27 Br O5P 21 21 216.202; 12.159; 30.276
90; 90; 90
2283.12Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119356 CIFC12 H8 I2 N O3C 1 2/c 117.6; 4.372; 34.3
90; 97.444; 90
2617Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119357 CIFC24 H16 Cl4 N2 O6P -13.795; 14.7; 21.4
80.7; 89.35; 89.09
1178Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119358 CIFC11 H8 Br2 N OP -14.183; 8.769; 15.366
94.1; 95.78; 99.68
550.5Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119359 CIFC9 H6 Cl2 N O3P -13.777; 10.382; 13.45
68.43; 85.15; 80.26
483.3Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119360 CIFC9 H6 I2 N O3C 1 2/c 127.78; 4.706; 17.566
90; 96.051; 90
2284Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119361 CIFC91.75 H99.7 Cl12.48 N14.43 O4.45 Pd6 S0.48P 1 21/c 119.6264; 52.3974; 14.3627
90; 90.6803; 90
14769.2Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119362 CIFC43 H52 Cl8 N6 O4 Pd3P 1 21/c 119.5796; 52.142; 14.2469
90; 91.162; 90
14541.9Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119363 CIFC94.65 H105.36 Cl12 N16.29 O3.82 Pd6 S0.41P 1 21/c 119.5493; 51.784; 14.2759
90; 90.7569; 90
14450.8Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119373 CIFC13 H17 N3 O3 S2P b c a10.4816; 12.7531; 22.3603
90; 90; 90
2989Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119374 CIFC32 H62 N4 O5 S3P -15.7565; 10.7037; 31.057
87.126; 85.544; 86.192
1901.7Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119375 CIFC20 H15 N O3P 21 21 215.5517; 11.006; 24.121
90; 90; 90
1473.8Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119376 CIFC25 H19 N O2C 1 2/c 137.27; 7.992; 12.774
90; 91.797; 90
3803Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119377 CIFC20 H15 Cl N2 O2P 21 21 217.174; 14.3271; 17.4194
90; 90; 90
1790.4Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119378 CIFC21 H18 Cl N O4P 21 21 217.1668; 12.4455; 21.2096
90; 90; 90
1891.78Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119379 CIFC62 H58 Gd2 N8 O20 Zn2P 1 21/c 113.8176; 14.3073; 16.9982
90; 95.502; 90
3344.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119380 CIFC62 H58 Dy2 N8 O20 Zn2P 1 21/c 113.75033; 14.3147; 16.9418
90; 95.2801; 90
3320.54Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119381 CIFC62 H58 N8 O20 Y2 Zn2P 1 21/c 113.7448; 14.3133; 16.9268
90; 95.068; 90
3317Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119382 CIFC62 H58 Eu2 N8 O20 Zn2P 1 21/c 113.8125; 14.3087; 16.9783
90; 95.498; 90
3340.14Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119383 CIFC23 H18 N2P 1 21/c 110.0681; 9.7551; 17.5082
90; 94.291; 90
1714.8Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119384 CIFC29 H24 N2 O2P -19.9468; 10.285; 11.5735
75.327; 82.383; 81.347
1126.82Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119385 CIFC23 H20 N2 O3P 1 21/n 18.8491; 10.6531; 20.9154
90; 96.794; 90
1957.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119386 CIFC25 H22 N2I 1 2/a 118.3322; 10.0821; 20.0451
90; 90.573; 90
3704.7Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119387 CIFC96 H92 N12 O32 Zr6F m -3 m29.983; 29.983; 29.983
90; 90; 90
26954Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119388 CIFC96 H80 O32 Zr6F m -3 m29.941; 29.941; 29.941
90; 90; 90
26841Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119389 CIFC36 H36 Cl6 Ge3 N4P 1 21/c 19.4771; 16.9192; 25.2949
90; 92.298; 90
4052.6Swamy, V. S. V. S. N.; Yadav, Sandeep; Pal, Shiv; Das, Tamal; Vanka, Kumar; Sen, Sakya S.
Facile access to a Ge(II) dication stabilized by isocyanides
Chemical Communications, 2016, 52, 7890-7892
7119440 CIFC29 H36 Br F3 N O3 PP 1 21/n 19.477; 15.308; 21.114
90; 102.525; 90
2990Ryosuke; Saijo; Hidemitsu; Uno; Shigeki; Mori; Masami; Kawase
Synthesis and structures of stable phosphorus zwitterions derived from mesoionic 4_trifluoroacetyl-1,3-oxazolium-5-olates
Chem.Commun., 2016, 52, 8006
7119441 CIFC39 H31 N O3 SP 4/n c c25.9455; 25.9455; 24.2457
90; 90; 90
16321.5Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119442 CIFC60 H45 N O3 SP 4/n c c26.7747; 26.7747; 24.0725
90; 90; 90
17257.2Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119443 CIFC62.5 H45 N O3 SP 4/n c c27.3864; 27.3864; 24.2386
90; 90; 90
18179.3Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119446 CIFC26 H28 F12 N6 P2 RuC 1 2/c 120.6432; 12.1018; 12.8802
90; 110.019; 90
3023.3Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119447 CIFC30 H32 F12 N6 P2 RuC 1 2 125.132; 9.8199; 17.2577
90; 131.012; 90
3213.8Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119448 CIFC24 H32 F12 N6 P2 RuP 31 2 110.2422; 10.2422; 24.9887
90; 90; 120
2270.18Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119449 CIFC25 H29 Cl F12 Fe N5 P2P 1 21 110.1753; 16.8389; 9.2498
90; 112.218; 90
1467.2Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119450 CIFC60 H74 B2 F8 N10 O20 Ru3P 1 21/n 114.515; 14.999; 15.692
90; 96.15; 90
3397Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119451 CIFC60 H82 B F4 N10 O32 Ru3 S2P -115.229; 17.001; 17.204
65.62; 84.91; 71.63
3845.9Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119454 CIFC36 H26 Cd N2 O4P 41 21 214.5436; 14.5436; 29.1864
90; 90; 90
6173.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119455 CIFC36 H25 Cd N2 O4P 43 21 214.573; 14.573; 28.941
90; 90; 90
6146Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119456 CIFC36 H26 Cd N2 O4P 43 21 214.523; 14.523; 29.1177
90; 90; 90
6141.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119457 CIFC36 H24 Cd N2 O4P 43 21 214.3555; 14.3555; 29.4087
90; 90; 90
6060.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119458 CIFC36 H26 Cd N2 O4P 41 21 214.5029; 14.5029; 29.2053
90; 90; 90
6142.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119459 CIFC36 H24 Cd N2 O4P 41 21 214.3664; 14.3664; 29.399
90; 90; 90
6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119460 CIFC36 H26 Cd N2 O4P 43 21 214.5318; 14.5318; 29.1429
90; 90; 90
6154.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119461 CIFC36 H26 Cd N2 O4P 41 21 214.5128; 14.5128; 29.194
90; 90; 90
6148.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119462 CIFC36 H26 Cd N2 O4P 43 21 214.4791; 14.4791; 29.069
90; 90; 90
6094.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119463 CIFC36 H26 Cd N2 O4P 43 21 214.4739; 14.4739; 29.0695
90; 90; 90
6089.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119464 CIFC36 H26 Cd N2 O4P 43 21 214.4958; 14.4958; 29.0361
90; 90; 90
6101.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119465 CIFC36 H26 Cd N2 O4P 43 21 214.5294; 14.5294; 29.1842
90; 90; 90
6160.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119466 CIFC36 H26 Cd N2 O4P 41 21 214.4838; 14.4838; 29.2182
90; 90; 90
6129.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119467 CIFC36 H26 Cd N2 O4P 41 21 214.4458; 14.4458; 29.3447
90; 90; 90
6123.7Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119468 CIFC36 H26 Cd N2 O4P 41 21 214.4171; 14.4171; 29.1929
90; 90; 90
6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119469 CIFC36 H26 Cd N2 O4P 41 21 214.5097; 14.5097; 28.8452
90; 90; 90
6072.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119470 CIFC36 H26 Cd N2 O4P 41 21 214.5222; 14.5222; 29.245
90; 90; 90
6167.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119471 CIFC36 H26 Cd N2 O4P 41 21 214.5387; 14.5387; 29.246
90; 90; 90
6181.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119472 CIFC36 H26 Cd N2 O4P 43 21 214.5486; 14.5486; 29.1966
90; 90; 90
6179.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119473 CIFC36 H26 Cd N2 O4P 43 21 214.486; 14.486; 28.911
90; 90; 90
6066.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119474 CIFC36 H26 Cd N2 O4P 41 21 214.4896; 14.4896; 29.1167
90; 90; 90
6113Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119475 CIFC36 H26 Cd N2 O4P 43 21 214.4789; 14.4789; 29.007
90; 90; 90
6081Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119476 CIFC36 H26 Cd N2 O4P 41 21 214.5067; 14.5067; 28.888
90; 90; 90
6079.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119477 CIFC36 H26 Cd N2 O4P 41 21 214.4975; 14.4975; 29.1189
90; 90; 90
6120.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119478 CIFC36 H26 Cd N2 O4P 43 21 214.5803; 14.5803; 29.181
90; 90; 90
6203.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119479 CIFC36 H26 Cd N2 O4P 41 21 214.5474; 14.5474; 29.2215
90; 90; 90
6184.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119480 CIFC36 H26 Cd N2 O4P 43 21 214.5616; 14.5616; 29.153
90; 90; 90
6181.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119481 CIFC36 H25 Cd N2 O4P 41 21 214.4906; 14.4906; 29.1148
90; 90; 90
6113.5Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119482 CIFC72 H40 In2 O16R -3 :H44.874; 44.874; 42.074
90; 90; 120
73373Panpan; Yu; Qipeng; Li; Yue; Hu; Nannan; Liu; Lijie; Zhang; Kongzhao; Su; Jinjie; Qian; Shaoming; Huang; Maochun; Hong
Cuboctahedron-based indium-organic frameworks for gas sorption and selective cation exchange
Chem.Commun., 2016, 52, 7978
7119483 CIFC25 H16 O3C 1 2/c 125.507; 8.1552; 16.661
90; 92.869; 90
3461.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119484 CIFC27 H22 O4P -19.173; 10.382; 12.748
104.062; 94.66; 116.023
1033.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119485 CIFC25 H26 O4P 1 21/n 114.1779; 7.8527; 19.28
90; 96.464; 90
2132.9Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119486 CIFC27 H24 O3P -15.7885; 10.4613; 16.3808
92.216; 97.607; 92.531
981.26Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119487 CIFC37.5 H32.5 Br Cl10.5 Mn N3 O3 P2P -112.8806; 15.305; 15.3667
113.734; 98.8175; 110.01
2452.06Gyandshwar; Kumar; Rao; Wendy; Pell; Ilia; Korobkov; Darrin; Richeson
Electrocatalytic reduction of CO2 using Mn complexes with unconventional coordination environments
Chem.Commun., 2016, 52, 8010
7119488 CIFC21 H17 Br Mn N2 O3 PP 1 21 18.312; 11.1704; 11.8045
90; 108.672; 90
1038.34Gyandshwar; Kumar; Rao; Wendy; Pell; Ilia; Korobkov; Darrin; Richeson
Electrocatalytic reduction of CO2 using Mn complexes with unconventional coordination environments
Chem.Commun., 2016, 52, 8010
7119615 CIFC219 H324 Gd18 N30 O147R -3 c :H33.1977; 33.1977; 59.4184
90; 90; 120
56711Kai; Wang; Zi-Lu; Chen; Hua-Hong; Zou; Kun; Hu; Hai-Ye; Li; Zhong; Zhang; Wei-Yin; Sun; Fu-Pei; Liang
A single-stranded {Gd18} nanowheel with a symmetric polydentate diacylhydrazone ligand
Chem.Commun., 2016, 52, 8297
7119616 CIFC15 H15 N O2P 21 21 217.965; 9.5073; 16.0506
90; 90; 90
1215.44Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119617 CIFC15 H15 N O2P 21 21 217.9647; 9.5076; 16.0492
90; 90; 90
1215.33Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119618 CIFC14 H12 Br N O2P 21 21 218.5431; 9.8089; 14.6636
90; 90; 90
1228.79Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119619 CIFC15 H15 N O3P 1 21/n 116.9222; 7.6509; 20.5384
90; 109.285; 90
2509.9Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119620 CIFC15 H12 F3 N O2P 1 21/c 19.6309; 7.8723; 17.274
90; 96.92; 90
1300.13Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119621 CIFC15 H12 F3 N O2P -18.7121; 11.7093; 14.2353
76.9998; 72.3793; 69.8941
1287.79Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119622 CIFC14 H12 Br N O2P 1 21/n 118.1984; 7.3629; 19.2858
90; 108.487; 90
2450.81Ramya Raghunathan; Elango Kumarasamy; Steffen Jockusch; Angel Ugrinov; J. Sivaguru
Engaging electronic effects for atropselective [5+2]-photocycloaddition of maleimides
Chem.Commun., 2016, 52, 8305
7119649 CIFC23 H20 Cl N O2P 21 21 219.4627; 11.1519; 18.1676
90; 90; 90
1917.17Yan Lu; Yuhang Zhou; Lili Lin; Haifeng Zheng; Kai Fu; Xiaohua Liu; Xiaoming Feng
N,N'-Dioxide/nickel(II)-catalyzed asymmetric Diels-Alder reaction of cyclopentadiene with 2,3-dioxopyrrolidines and 2=alkenoyl pyridines
Chem.Commun., 2016, 52, 8255
7119650 CIFC18 H21 N O4P 21 21 2116.2716; 21.2062; 10.0994
90; 90; 90
3484.9U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119651 CIFC18 H21 N O4P 1 21 19.882; 20.953; 16.215
90; 93.913; 90
3350U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119652 CIFC18 H21 N O4P 1 21/c 110.0661; 21.081; 16.584
90; 100.06; 90
3465.1U. B. Rao Khandavilli; Matteo Lusi; Balakrishna R. Bhogala; Anita R. Maguire; Matthias Stein; Simon E. Lawrence
Diversity in a simple co-crystal: racemic and kryptoracemic behaviour
Chem.Commun., 2016, 52, 8309-8312
7119653 CIFC11 H16 N2 O5 SP 1 21/n 19.03667; 6.90757; 21.7122
90; 99.8233; 90
1335.44Shuai Dong; Kiran Indukuri; Derrick L. J. Clive; Jin-Ming Gao
Synthesis of models of the BC ring systems of MPC1001 and MPC1001F
Chem.Commun., 2016, 52, 8271
7119654 CIFC16 H15 N3 O7 SP -16.7169; 7.9571; 16.1794
91.3062; 98.1391; 92.2828
855Shuai Dong; Kiran Indukuri; Derrick L. J. Clive; Jin-Ming Gao
Synthesis of models of the BC ring systems of MPC1001 and MPC1001F
Chem.Commun., 2016, 52, 8271
7119655 CIFC16 H14 F3 N3 O2P 1 21/c 110.013; 7.5562; 21.159
90; 93.102; 90
1598.5Xing-Long Yu; Jia-Rong Chen; Dong-Zhen Chen; Wen-Jing Xiao
Visible-light-induced photocatalytic azotrifluoromethylation of alkenes with aryldiazonium salts and sodium triflinate
Chem.Commun., 2016, 52, 8275
7119656 CIFC20 H17 B F4 OP 1 21/n 17.7761; 15.354; 14.48
90; 95.766; 90
1720.1Eliar Mosaferi; David Ripsman; Douglas W. Stephan
The air-stable carbocation salt [(MeOC6H4)CPh2][BF4] in Lewis acid catalyzed hydrothiolation of alkenes
Chem.Commun., 2016, 52, 8291
7119675 CIFC59 H59 B2 F24 N5 PtC 1 2/c 139.65; 13.44; 26.01
90; 111.476; 90
12898Marta Rosello-Merino; Raquel J. Rama; Josefina Diez; Salvador Conejero
Catalytic dehydrocoupling of amine-boranes and amines into diaminoboranes: isolation of a Pt(II), Shimoi-type, Eta1-BH complex
Chem.Commun., 2016, 52, 8389
7119676 CIFC68 H78 N8 O28 Zn3I -4 2 d28.2219; 28.2219; 9.7266
90; 90; 90
7747Jun-Cheng Jin; Ju Wu; Guo-Ping Yang; Yun-Long Wu; Yao-Yu Wang
A microporous anionic metal-organic framework for a highly selective and sensitive electrochemical sensor of Cu2+ ions
Chem.Commun., 2016, 52, 8475
7119677 CIFC19 H12 O4P -18.4472; 12.7834; 15.0002
100.217; 105.699; 108.939
1411Devenderan Ramanathan; Kayambu Namitharan; Kasi Pitchumani
Copper(I)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones
Chem.Commun., 2016, 52, 8436
7119678 CIFC18.25 H10.5 O3P 1 21/n 19.081; 15.7891; 9.2543
90; 97.431; 90
1315.74Devenderan Ramanathan; Kayambu Namitharan; Kasi Pitchumani
Copper(I)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones
Chem.Commun., 2016, 52, 8436
7119679 CIFC73 H82 Cl4 Co3 N10 O26P 1 21 114.3957; 18.2215; 16.1798
90; 102.476; 90
4143.9Roberto Berardozzi; Elena Badetti; Nadia Alessandra Carmo dos Santos; Klaus Wurst; Giulia Licini; Gennaro Pescitelli; Cristiano Zonta; Lorenzo Di Bari
Co(II)-induced giant vibrational CD provides a new design of methods for rapid and sensitive chirality recognition
Chem.Commun., 2016, 52, 8428
7119680 CIFC21 H17 N O3 S SeP -19.7234; 9.8305; 22.0952
102.367; 94.393; 107.218
1948.22Kai Sun; Xin Wang; Yunhe Lv; Gang Li; Hezhen Jiao; Changwei Dai; Yangyang Li; Chong Zhang; Lin Liu
Peroxodisulfate-mediated selenoamination of alkenes yielding amidoselenide-containing sulfamides and azoles
Chem.Commun., 2016, 52, 8471
7119681 CIFC24 H27 Co3 N12 O10P 63/m m c16.8676; 16.8676; 18.8186
90; 90; 120
4636.9Di-Ming Chen; Jia-Yue Tian; Chun-Sen Liu; Miao Du
A bracket approach to improve the stability and gas sorption performance of a metal-organic framework via in situ incorporating the size-matching molecular building blocks
Chem. Commun., 2016, 52, 8413
7119682 CIFC42 H24 Co5 N15 O15P 63/m m c18.8605; 18.8605; 16.6183
90; 90; 120
5119.5Di-Ming Chen; Jia-Yue Tian; Chun-Sen Liu; Miao Du
A bracket approach to improve the stability and gas sorption performance of a metal-organic framework via in situ incorporating the size-matching molecular building blocks
Chem. Commun., 2016, 52, 8413
7119826 CIFC193.68 H54 Cu18 N18 O117R -3 m18.2623; 18.2623; 39.6543
90; 90; 120
11453.3Xiaoping Zhang; Zhenjie Zhang; Jake Boissonnault; Seth M. Cohen
Design and synthesis of squaramide-based MOFs as efficient MOF-supported hydrogen-bonding organocatalysts
Chem.Commun., 2016, 52, 8585
7119827 CIFC180 H54 N18 O108 Zn18R -3 m18.816; 18.816; 38.416
90; 90; 120
11779Xiaoping Zhang; Zhenjie Zhang; Jake Boissonnault; Seth M. Cohen
Design and synthesis of squaramide-based MOFs as efficient MOF-supported hydrogen-bonding organocatalysts
Chem.Commun., 2016, 52, 8585
7119828 CIFC19 H21 B Cd N9 O4P -18.562; 8.839; 16.904
82.238; 89.592; 78.252
1240.7Min Liu; Shumei Chen; Tian Wen; Jian Zhang
Encapsulation of LnIII ions/Ag nanoparticles within Cd(II) boron imidazolate frameworks for tuning luminescence emission
Chem.Commun., 2016, 52, 8577
7119829 CIFC42 H31 B2 Cd3 N16 O12C 1 2/c 128.187; 14.002; 27.657
90; 116.228; 90
9792Min Liu; Shumei Chen; Tian Wen; Jian Zhang
Encapsulation of LnIII ions/Ag nanoparticles within Cd(II) boron imidazolate frameworks for tuning luminescence emission
Chem.Commun., 2016, 52, 8577
7119830 CIFC52 H68 N8 O8P 1 21/n 117.4535; 8.0246; 17.7712
90; 97.847; 90
2465.68Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119831 CIFC286 H338 N38 O40 Pr4P -120.6712; 21.0386; 21.6281
62.477; 79.558; 67.086
7683.2Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119832 CIFC60 H68 N16 O4 Pr2C 1 2 128.896; 8.6749; 14.2513
90; 116.056; 90
3209.29Juhoon Lee; Nolan W. Waggoner; Luis Polanco; Ga Rim You; Vincent M. Lynch; Sung Kuk Kim; Simon M. Humphrey; Jonathan L. Sessler
Ship in a breakable bottle: fluoride-induced release of an organic molecule from a Pr(III)-linked molecular cage
Chem.Commun., 2016, 52, 8514
7119833 CIFC21 H22 N2 O5P 1 21/n 114.2787; 9.4954; 14.5637
90; 98.003; 90
1955.34Yanan Li; Huihui Gao; Zhenlei Zhang; Peng Qian; Meixiang Bi; Zhenggen Zha; Zhiyong Wang
Electrochemical synthesis of alpha-enaminones from aryl ketones
Chem.Commun., 2016, 52, 8600
7120018 CIFC29 H46 N4 O2 S4P -18.58; 13.5581; 13.8786
85.002; 87.556; 85.019
1601.26Luyi Zong; Yujun Xie; Can Wang; Jian-Rong Li; Qianqian Li; Zhen Li
From ACQ to AIE: the suppression of the strong pi-pi interaction of naphthalene diimide derivatives through the adjustment of their flexible chains
Chem.Commun., 2016, 52, 11496
7121007 CIFC37 H43 N3 O3 S2P 1 21/c 114.0664; 27.41; 9.4754
90; 107.434; 90
3485.5Chris L. Vonnegut; Airlia M. Shonkwiler; Lev N. Zakharov; Michael M. Haley; Darren W. Johnson
Harnessing solid-state packing for selective detection of chloride in a macrocyclic anionophore
Chemical Communications, 2016, 52, 9506-9509
7121008 CIFC38.25 H44.5 Cl3.5 N3 O2 S2P 1 21/n 120.7737; 31.7155; 24.6016
90; 98.088; 90
16047.5Chris L. Vonnegut; Airlia M. Shonkwiler; Lev N. Zakharov; Michael M. Haley; Darren W. Johnson
Harnessing solid-state packing for selective detection of chloride in a macrocyclic anionophore
Chemical Communications, 2016, 52, 9506-9509
7121015 CIFC13 H54 N2 Na2 Ni O34 W6P -19.6825; 10.3943; 11.758
113.733; 102.543; 90.479
1051.34Nadiia I. Gumerova; Alexander Roller; Annette Rompel
[Ni(OH)3W6O18(OCH2)3CCH2OH]4-: the first tris-functionalized Anderson-type heteropolytungstate
Chemical Communications, 2016, 52, 9263-9266
7124582 CIFC31 H34 Cl2 N2 O3P 1 21/c 19.4917; 18.4515; 16.3576
90; 100.11; 90
2820.3Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124583 CIFC31 H35 Cl N2 O2P 1 21/c 110.4748; 17.8218; 15.4388
90; 105.179; 90
2781.6Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124584 CIFC35 H43 Cl3 N2 OP -111.4742; 11.8275; 12.891
81.869; 87.309; 88.774
1729.8Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124585 CIFC31 H33 N2 O3P 1 21/c 111.8892; 16.2557; 13.7767
90; 96.327; 90
2646.4Deardorff, Cassie L.; Eric Sikma, R.; Rhodes, Christopher P.; Hudnall, Todd W.
Carbene-derived α-acyl formamidinium cations: organic molecules with readily tunable multiple redox processes.
Chemical communications (Cambridge, England), 2016, 52, 9024-9027
7124586 CIFC10 H10 N8 O S2P 1 21/n 19.3608; 11.0691; 13.0914
90; 110.3; 90
1272.2Kersten, Kortney M.; Matzger, Adam J.
Improved pharmacokinetics of mercaptopurine afforded by a thermally robust hemihydrate.
Chemical communications (Cambridge, England), 2016, 52, 5281-5284
7124587 CIFC54 H40 N2P b c a11.0573; 25.485; 28.816
90; 90; 90
8120.2Dai, Shengyu; Sui, Xuelin; Chen, Changle
Synthesis of high molecular weight polyethylene using iminopyridyl nickel catalysts.
Chemical communications (Cambridge, England), 2016, 52, 9113-9116
7124588 CIFC25 H22 N2 O4P 1 21/c 111.398; 11.272; 16.887
90; 98.34; 90
2146.7Wang, Nan-Nan; Hao, Wen-Juan; Zhang, Tian-Shu; Li, Guigen; Wu, Ya-Nan; Tu, Shu-Jiang; Jiang, Bo
Metal-free C(sp(3))-H functionalization: oxidative carbo-oxygenation of α-diazo carbonyls via radical dediazotization.
Chemical communications (Cambridge, England), 2016, 52, 5144-5147
7124589 CIFC14 H16 O3P 1 21/n 114.498; 5.9876; 14.857
90; 103.208; 90
1255.6Bankar, Siddheshwar K.; Mathew, Jopaul; Ramasastry, S. S. V.
Synthesis of benzofurans via an acid catalysed transacetalisation/Fries-type O →C rearrangement/Michael addition/ring-opening aromatisation cascade of β-pyrones.
Chemical communications (Cambridge, England), 2016, 52, 5569-5572
7124590 CIFC28 H30 Br2 O6P -17.84; 11.999; 15.345
102.86; 98.09; 90.08
1392.5Bankar, Siddheshwar K.; Mathew, Jopaul; Ramasastry, S. S. V.
Synthesis of benzofurans via an acid catalysed transacetalisation/Fries-type O →C rearrangement/Michael addition/ring-opening aromatisation cascade of β-pyrones.
Chemical communications (Cambridge, England), 2016, 52, 5569-5572
7124591 CIFC27 H30 N2 O6 SP 21 21 218.931; 10.538; 28.633
90; 90; 90
2695Zhang, Minmin; Yu, Shuowen; Hu, Fangzhi; Liao, Yijun; Liao, Lihua; Xu, Xiaoying; Yuan, Weicheng; Zhang, Xiaomei
Highly enantioselective [3+2] coupling of cyclic enamides with quinone monoimines promoted by a chiral phosphoric acid.
Chemical communications (Cambridge, England), 2016, 52, 8757-8760
7124592 CIFC15 H24 B N O2P 1 21/n 113.8539; 7.816; 15.243
90; 115.863; 90
1485.22Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124593 CIFC16 H26 B F2 N OP 1 21/n 17.6884; 13.7157; 15.1094
90; 98.435; 90
1576.1Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124594 CIFC15 H23 B F3 NP 1 21/c 114.8666; 7.633; 14.4543
90; 115.531; 90
1480.06Légaré, Marc-André; Rochette, Étienne; Légaré Lavergne, Julien; Bouchard, Nicolas; Fontaine, Frédéric-Georges
Bench-stable frustrated Lewis pair chemistry: fluoroborate salts as precatalysts for the C-H borylation of heteroarenes.
Chemical communications (Cambridge, England), 2016, 52, 5387-5390
7124595 CIFC21 H32 Cl N OP 21 21 2111.6015; 12.822; 13.428
90; 90; 90
1997.5McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124596 CIFC21 H31 N OP 1 21/c 18.9044; 11.5431; 17.771
90; 92.232; 90
1825.2McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124597 CIFC31 H41 N OP 1 21/n 18.6897; 29.0766; 10.8005
90; 106.809; 90
2612.3McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124598 CIFC29 H43 Cl Ir N OP 1 21/c 115.8695; 11.8315; 14.6016
90; 96.061; 90
2726.3McCarty, Zachary R.; Lastovickova, Dominika N.; Bielawski, Christopher W.
A cyclic (alkyl)(amido)carbene: synthesis, study and utility as a desulfurization reagent.
Chemical communications (Cambridge, England), 2016, 52, 5447-5450
7124599 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.8011; 14.62079; 21.27781
90; 90; 90
6160.09Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124600 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.9769; 14.811; 21.41308
90; 90; 90
6335.66Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124601 CIFC23 H7 F18 N3 O7 S2 SmP b c a20.0503; 14.9396; 21.463
90; 90; 90
6429.1Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124602 CIFC23 H7 F18 N3 O7 S2 SmP b c a20.1162; 15.14532; 21.5437
90; 90; 90
6563.64Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124603 CIFC23 H7 F18 N3 O7 S2 SmP b c a19.85308; 14.68673; 21.32145
90; 90; 90
6216.84Fatila, Elisabeth M.; Maahs, Adam C.; Mills, Michelle B.; Rouzières, Mathieu; Soldatov, Dmitriy V.; Clérac, Rodolphe; Preuss, Kathryn E.
Ferromagnetic ordering of -[Sm(iii)-radical]n- coordination polymers.
Chemical communications (Cambridge, England), 2016, 52, 5414-5417
7124604 CIFC62.5 H70 N4 Ni2 P4P -112.4093; 13.1987; 18.3557
79.4323; 76.229; 84.6926
2866.71Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124605 CIFC76.5 H83 N5 Ni2 P4 SP -113.6251; 14.0607; 19.7007
99.8667; 99.819; 98.0922
3607.33Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124606 CIFC73 H79 N5 Ni2 P4 SP -112.4533; 15.594; 19.3068
104.227; 103.128; 106.371
3305.15Pelties, Stefan; Ehlers, Andreas W.; Wolf, Robert
Insertion of phenyl isothiocyanate into a P-P bond of a nickel-substituted bicyclo[1.1.0]tetraphosphabutane.
Chemical communications (Cambridge, England), 2016, 52, 6601-6604
7124607 CIFC51 H38 Al B F20 N2P 1 21/n 114.3392; 22.0014; 16.1601
90; 107.299; 90
4867.6Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124608 CIFC17 H19 Al N2P 1 21/n 111.8284; 11.5141; 12.6491
90; 113.135; 90
1584.2Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124609 CIFC88 H38 Al B2 Br F40 N4P -112.4696; 13.5438; 23.9484
89.208; 88.213; 79.504
3974.8Cao, Levy L.; Daley, Erika; Johnstone, Timothy C.; Stephan, Douglas W.
Cationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borate.
Chemical communications (Cambridge, England), 2016, 52, 5305-5307
7124610 CIFC17 H15 Br O2P 1 21 15.9605; 32.909; 7.1915
90; 91.991; 90
1409.8Kondoh, Azusa; Tran, Hoa Thi Quynh; Kimura, Kyoko; Terada, Masahiro
Enantioselective intramolecular cyclization of alkynyl esters catalyzed by a chiral Brønsted base.
Chemical communications (Cambridge, England), 2016, 52, 5726-5729
7124611 CIFC29 H27 N3 O3P 1 21/n 117.181; 26.757; 21.323
90; 96.526; 90
9739Selvaraju, Manikandan; Ye, Tzuen-Yang; Li, Chia-Hsin; Ho, Pei-Heng; Sun, Chung-Ming
Copper catalyzed aerobic oxidative cyclization and ketonization: one pot synthesis of benzoimidazo[1,2-a]imidazolones.
Chemical communications (Cambridge, England), 2016, 52, 6621-6624
7124612 CIFC36 H44 Cl6 Cu N4 O4P -111.6428; 13.6677; 14.1795
84.481; 68.11; 72.003
1990.8Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124613 CIFC37 H44 N4 O4 ZnP -111.175; 11.683; 14.705
92.05; 105.445; 110.322
1717.8Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124614 CIFC35 H44 Cl2 Co N4 O4C 1 2/c 117.3525; 13.834; 14.8976
90; 102.894; 90
3486.1Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124615 CIFC36 H42 Cl6 D2 N4 Ni O4P -112.2982; 14.0284; 14.0382
76.426; 67.944; 64.685
2021.2Gautam, R.; Chang, T. M.; Astashkin, A. V.; Lincoln, K. M.; Tomat, E.
Propentdyopent: the scaffold of a heme metabolite as an electron reservoir in transition metal complexes.
Chemical communications (Cambridge, England), 2016, 52, 6585-6588
7124616 CIFC342 H280 B16 Co8 F64 N72 O3.5 PC 1 2/c 132.8826; 30.1786; 40.0732
90; 96.498; 90
39511.2Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124617 CIFC343 H281 B16 Co8 F64 N72 O3 PC 1 2/c 132.7148; 29.7919; 39.8554
90; 96.733; 90
38576.6Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124618 CIFC366 H330 B16 Co8 F64 N72 O30 P2C 1 2/c 127.477; 39.201; 41.992
90; 107.133; 90
43223Taylor, Christopher G. P.; Piper, Jerico R.; Ward, Michael D.
Binding of chemical warfare agent simulants as guests in a coordination cage: contributions to binding and a fluorescence-based response.
Chemical communications (Cambridge, England), 2016, 52, 6225-6228
7124619 CIFC60 H56 Cl2 O8C 1 2/c 112.0691; 21.178; 20.726
90; 105.081; 90
5115.1Ma, Yingjie; Chen, Long; Li, Chen; Müllen, Klaus
A fishing rod-like conjugated polymer bearing pillar[5]arenes.
Chemical communications (Cambridge, England), 2016, 52, 6662-6664
7124620 CIFC39 H54 N3 NbP 19.6363; 10.354; 10.4978
107.019; 113.605; 91.585
905.11Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124621 CIFC39 H55 N6 NbP 1 21/n 111.649; 18.9555; 17.0768
90; 97.526; 90
3738.3Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124622 CIFC38 H49 N3 NbP n n m12.4801; 13.772; 19.2824
90; 90; 90
3314.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124623 CIFC67 H72 B F15 N5 NbP -112.5396; 17.4757; 29.99
84.127; 82.987; 73.602
6241.6Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124624 CIFC57 H55 B F15 N6 NbP -112.2684; 12.7008; 19.2268
79.4526; 83.1067; 68.923
2743.4Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124625 CIFC121 H118 B2 F30 N8 Nb2P b c a19.3473; 22.4336; 25.5172
90; 90; 90
11075.2Camp, Clément; Grant, Lauren N.; Bergman, Robert G.; Arnold, John
Photo-activation of d(0) niobium imido azides: en route to nitrido complexes.
Chemical communications (Cambridge, England), 2016, 52, 5538-5541
7124626 CIFC15 H32 Cu3 N12 O16P -112.6421; 14.2612; 17.0125
90.192; 96.38; 113.941
2782Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124627 CIFC15 H44 Cl3 N9 Ni3 O13P 1 21/c 117.1605; 13.4761; 14.8097
90; 111.774; 90
3180.5Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124628 CIFC18 H32 N8 O14 U2P 1 21/n 18.3529; 21.2854; 8.9198
90; 111.884; 90
1471.61Kennedy, Zachary C.; Cardenas, Allan Jay P.; Corbey, Jordan F.; Warner, Marvin G.
2,6-Diiminopiperidin-1-ol: an overlooked motif relevant to uranyl and transition metal binding on poly(amidoxime) adsorbents.
Chemical communications (Cambridge, England), 2016, 52, 8802-8805
7124629 CIFC31 H32 F2 I N O4 SP 1 21/c 114.4081; 22.6704; 19.5045
90; 109.072; 90
6021.2Yu, Liu-Zhu; Zhu, Zi-Zhong; Hu, Xu-Bo; Tang, Xiang-Ying; Shi, Min
Palladium-catalyzed cascade cyclization of allylamine-tethered alkylidenecyclopropanes: facile access to iodine/difluoromethylene- and perfluoroalkyl-containing 1-benzazepine scaffolds.
Chemical communications (Cambridge, England), 2016, 52, 6581-6584
7124630 CIFC30 H36 B F2 PP -19.9138; 10.3236; 13.6951
76.806; 71.844; 82.615
1294.2Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124631 CIFC54 H32 B2 F25 PP 1 21 110.7299; 19.7985; 12.1281
90; 95.89; 90
2562.84Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124632 CIFC30 H32 B F6 PP 1 21/n 111.4351; 9.5654; 24.6131
90; 92.863; 90
2688.9Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124633 CIFC54 H36 B2 F21 PP -19.9916; 15.7747; 16.8287
86.925; 79.345; 75.871
2527.8Möbus, Juri; Vom Stein, Thorsten; Stephan, Douglas W.
Cooperative Lewis acidity in borane-substituted fluorophosphonium cations.
Chemical communications (Cambridge, England), 2016, 52, 6387-6390
7124634 CIFC11 H13 N O2P 1 21/n 18.9638; 10.52; 11.467
90; 109.75; 90
1017.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124635 CIFC11 H12 F N O2P 1 21/c 17.7034; 22.119; 12.573
90; 105.27; 90
2066.7Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124636 CIFC12 H15 N O3P 1 21/n 17.4266; 11.889; 13.141
90; 102.2; 90
1134.1Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124637 CIFC11 H12 F N O2P 1 21/n 19.0682; 10.39; 11.58
90; 109.17; 90
1030.6Tang, Baolei; Liu, Huapeng; Li, Feng; Wang, Yue; Zhang, Hongyu
Single-benzene solid emitters with lasing properties based on aggregation-induced emissions.
Chemical communications (Cambridge, England), 2016, 52, 6577-6580
7124638 CIFC158 H178 Au24 Pd S18P -116.1244; 17.6398; 17.7651
65.152; 64.342; 81.391
4129.8Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124639 CIFC158 H178 Au24 Pt S18P -116.19; 17.714; 17.8666
65.106; 64.289; 81.343
4184.5Tian, Shubo; Liao, Lingwen; Yuan, Jinyun; Yao, Chuanhao; Chen, Jishi; Yang, Jinlong; Wu, Zhikun
Structures and magnetism of mono-palladium and mono-platinum doped Au25(PET)18 nanoclusters.
Chemical communications (Cambridge, England), 2016, 52, 9873-9876
7124640 CIFC44 H42 Co4 N4 O14P 42/m b c25.569; 25.569; 16.707
90; 90; 90
10923Su, Lei; Song, Wei-Chao; Zhao, Jiong-Peng; Liu, Fu-Chen
Crystal engineering to control the magnetic interaction between weak ferromagnetic single-chain magnets assembled in a 3D framework.
Chemical communications (Cambridge, England), 2016, 52, 8722-8725
7124641 CIFC43 H51 Cl3 Co N2 O2 S2P 1 21/c 119.3263; 9.6193; 25.4228
90; 108.384; 90
4485Sarkar, Prasenjit; Tiwari, Archana; Sarmah, Amrit; Bhandary, Subhrajyoti; Roy, Ram Kinkar; Mukherjee, Chandan
An elusive vinyl radical isolated as an appended unit in a five-coordinate Co(iii)-bis(iminobenzosemiquinone) complex formed via ligand-centered C-S bond cleavage.
Chemical communications (Cambridge, England), 2016, 52, 10613-10616
7124642 CIFC21 H15 O7 PP 1 21/n 17.7879; 20.327; 11.9549
90; 93.558; 90
1888.9Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124643 CIFC60 H60 N6 O8 P2P 21 319.1327; 19.1327; 19.1327
90; 90; 90
7003.7Feng, Genfeng; Liu, Wei; Peng, Yuxin; Zhao, Bo; Huang, Wei; Dai, Yafei
Cavity partition and functionalization of a [2+3] organic molecular cage by inserting polar P[double bond, length as m-dash]O bonds.
Chemical communications (Cambridge, England), 2016, 52, 9267-9270
7124644 CIFC38 H32 F12 N4 P2P -18.8259; 9.7216; 12.7688
104.695; 100.791; 108.868
958.4Wang, Zhaoyang; Bai, Wei; Tong, Jiaqi; Wang, Yi Jia; Qin, Anjun; Sun, Jing Zhi; Tang, Ben Zhong
A macrocyclic 1,4-bis(4-pyridylethynyl)benzene showing unique aggregation-induced emission properties.
Chemical communications (Cambridge, England), 2016, 52, 10365-10368
7124645 CIFC21 H27 N3 O4I 1 2 116.8244; 6.0896; 41.9414
90; 101.245; 90
4214.6Li, Dan; Wang, Yijie; Wang, Linqing; Wang, Jie; Wang, Pengxin; Wang, Kezhou; Lin, Li; Liu, Dongsheng; Jiang, Xianxing; Yang, Dongxu
Simple magnesium catalyst mediated γ-butyrolactams in desymmetrization of meso-aziridines.
Chemical communications (Cambridge, England), 2016, 52, 9640-9643
7124646 CIFC18 H13 N OP 1 21/c 110.016; 9.223; 13.978
90; 94.662; 90
1287Wu, Shanchao; Liu, Na; Dong, Guoqiang; Ma, Lin; Wang, Shengzheng; Shi, Wencai; Fang, Kun; Chen, Shuqiang; Li, Jian; Zhang, Wannian; Sheng, Chunquan; Wang, Wei
Facile construction of pyrrolo[1,2-b]isoquinolin-10(5H)-ones via a redox-amination-aromatization-Friedel-Crafts acylation cascade reaction and discovery of novel topoisomerase inhibitors.
Chemical communications (Cambridge, England), 2016, 52, 9593-9596
7124647 CIFC36 H45 F12 N7 O4 P2 RuP -18.4109; 11.4169; 11.725
74.801; 76.758; 87.087
1057.59He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124648 CIFC29 H32 F12 N6 O3 P2 Ru SP 1 21/c 111.5273; 12.9572; 24.0256
90; 97.6261; 90
3556.8He, Lei; Chen, Xiang; Meng, Zhenyu; Wang, Jintao; Tian, Keyin; Li, Tianhu; Shao, Fangwei
Octahedral ruthenium complexes selectively stabilize G-quadruplexes.
Chemical communications (Cambridge, England), 2016, 52, 8095-8098
7124649 CIFC64 H59 Cl2 N6 O14P 21 21 2115.8312; 18.6954; 21.7724
90; 90; 90
6444Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124650 CIFC29 H24 Cl N3 O8P 15.8187; 11.7632; 11.9555
79.413; 87.509; 78.478
788.2Liu, Kang; Xiong, Yong; Wang, Zuo-Fei; Tao, Hai-Yan; Wang, Chun-Jiang
Ligand-controlled stereodivergent 1,3-dipolar cycloaddition of azomethine ylides with 3-methyl-4-nitro-5-styrylisoxazoles.
Chemical communications (Cambridge, England), 2016, 52, 9458-9461
7124651 CIFC25 H31 B Br4 Ga PP 1 21/n 112.2483; 15.51; 15.3013
90; 90.094; 90
2906.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124652 CIFC18 H21 B F6 N O4 P S2P b c n30.337; 7.7017; 19.3533
90; 90; 90
4521.8Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124653 CIFC34 H26 B Br4 Ga N PP 1 21/n 112.5932; 14.1435; 19.2716
90; 107.068; 90
3281.3Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124654 CIFC31 H29 B N PP 1 21/n 16.9184; 22.8078; 16.1979
90; 101.927; 90
2500.7Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124655 CIFC33 H30 B F6 N2 O4 P S2P -18.9898; 12.2194; 15.5624
91.453; 91.387; 106.552
1637.28Devillard, Marc; Mallet-Ladeira, Sonia; Bouhadir, Ghenwa; Bourissou, Didier
Diverse reactivity of borenium cations with >N-H compounds.
Chemical communications (Cambridge, England), 2016, 52, 8877-8880
7124656 CIFC12 H10 N4 O4 ZnP 43 21 27.8691; 7.8691; 22.353
90; 90; 90
1384.2Cepeda, Javier; Sebastian, Eider San; Padro, Daniel; Rodríguez-Diéguez, Antonio; García, Jose A; Ugalde, Jesus M.; Seco, Jose M.
A Zn based coordination polymer exhibiting long-lasting phosphorescence.
Chemical communications (Cambridge, England), 2016, 52, 8671-8674
7124657 CIFC21 H19 B O2P 1 21/a 114.9097; 6.6345; 16.6553
90; 92.822; 90
1645.52Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124658 CIFC22 H21 B O2P 1 21/c 111.7096; 10.8168; 14.2151
90; 91.551; 90
1799.8Wang, Taisheng; Zhang, Na; Zhang, Ke; Dai, Jingwen; Bai, Wei; Bai, Ruke
Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature.
Chemical communications (Cambridge, England), 2016, 52, 9679-9682
7124659 CIFC42 F28P 21 21 218.45; 11.0004; 42.68
90; 90; 90
3967.3Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124660 CIFC42 F28P 1 21/n 116.6651; 11.1489; 19.1918
90; 90.213; 90
3565.8Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124661 CIFC42 F28P -112.5285; 17.8163; 24.7339
90.202; 101.264; 90.695
5414Zhang, Zhuoran; Ogden, William A.; Young, Victor G.; Douglas, Christopher J.
Synthesis, electrochemical properties, and crystal packing of perfluororubrene.
Chemical communications (Cambridge, England), 2016, 52, 8127-8130
7124662 CIFC44 H61 N O10P -112.0803; 12.3966; 14.483
106.375; 96.145; 108.074
1932.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124663 CIFC125 H227 N10 O31.5P -113.3506; 15.7389; 17.8889
69.234; 75.125; 87.036
3393.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Kalenius, Elina; Ras, Robin H. A.; Rissanen, Kari
2-Methylresorcinarene: a very high packing coefficient in a mono-anion based dimeric capsule and the X-ray crystal structure of the tetra-anion.
Chemical communications (Cambridge, England), 2016, 52, 8115-8118
7124664 CIFC98 H120 N16 O18P 43 21 215.4204; 15.4204; 43.9852
90; 90; 90
10459.2Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124665 CIFC68 H80 N16 O12P 21 21 2122.2194; 26.8073; 30.7909
90; 90; 90
18340.4Chung, Mee-Kyung; Lee, Stephen J.; Waters, Marcey L.; Gagné, Michel R
Tetrameric psuedo-peptide receptors with allosteric properties.
Chemical communications (Cambridge, England), 2016, 52, 8103-8106
7124666 CIFC31 H35 N O2 SiP 1 21/n 110.5604; 12.5871; 20.6289
90; 103.411; 90
2667.3Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124667 CIFC31 H33 N O2 SiP 1 21/c 117.0259; 19.7058; 8.2013
90; 101.746; 90
2694Shinde, Popat S.; Shaikh, Aslam C.; Patil, Nitin T.
Efficient access to alkynylated quinalizinones via the gold(i)-catalyzed aminoalkynylation of alkynes.
Chemical communications (Cambridge, England), 2016, 52, 8152-8155
7124668 CIFC78 H68 Cl2 F6 N4 Pt2 S2P 1 21/c 112.1203; 21.6638; 27.3069
90; 91.372; 90
7168Boixel, Julien; Zhu, Yifan; Le Bozec, Hubert; Benmensour, Mohamed Ali; Boucekkine, Abdou; Wong, Keith Man-Chung; Colombo, Alessia; Roberto, Dominique; Guerchais, Véronique; Jacquemin, Denis
Contrasted photochromic and luminescent properties in dinuclear Pt(ii) complexes linked through a central dithienylethene unit.
Chemical communications (Cambridge, England), 2016, 52, 9833-9836
7124669 CIFC34 H58 F4 Mo N6 P4P 1 n 110.2417; 18.3288; 21.5881
90; 95.3341; 90
4034.93Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124670 CIFC34 H58 Cr F4 N6 P4P 1 21/c 110.8985; 13.441; 13.4741
90; 101.392; 90
1934.89Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124671 CIFC34 H58 Cr F4 N6 P4P 1 21/n 110.301; 18.8047; 20.7192
90; 93.77; 90
4004.77Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124672 CIFC34 H58 F4 N6 P4 WP 1 n 110.2469; 18.3292; 21.5498
90; 95.426; 90
4029.29Egbert, Jonathan D.; O'Hagan, Molly; Wiedner, Eric S.; Bullock, R. Morris; Piro, Nicholas A.; Kassel, W. Scott; Mock, Michael T.
Putting chromium on the map for N2 reduction: production of hydrazine and ammonia. A study of cis-M(N2)2 (M = Cr, Mo, W) bis(diphosphine) complexes.
Chemical communications (Cambridge, England), 2016, 52, 9343-9346
7124673 CIFC105 H105 N5P b c a32.7165; 16.1948; 39.103
90; 90; 90
20718.2Qiao, Bo; Anderson, Joseph R.; Pink, Maren; Flood, Amar H.
Size-matched recognition of large anions by cyanostar macrocycles is saved when solvent-bias is avoided.
Chemical communications (Cambridge, England), 2016, 52, 8683-8686
7124674 CIFC17 H13 N O2P 1 21/c 18.9419; 20.446; 7.9832
90; 111.874; 90
1354.5Li, Jiu-Ling; Li, Wei-Ze; Wang, Ying-Chun; Ren, Qiu; Wang, Heng-Shan; Pan, Ying-Ming
Palladium(ii)-catalyzed C-C and C-O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10028-10031
7124675 CIFC9 H9 N O3P 21 21 215.43; 7.8748; 20.6997
90; 90; 90
885.12Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124676 CIFC14 H11 N O3P 1 21 18.6028; 6.2292; 11.4861
90; 94.415; 90
613.7Vidal-Albalat, A; Swiderek, K.; Izquierdo, J.; Rodríguez, S; Moliner, V.; González, F V
Catalytic enantioselective epoxidation of nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 10060-10063
7124677 CIFC42 H76 Cl3 Dy O35P -112.741; 13.235; 17.923
89.94; 85.741; 86.594
3008.6Al Hareri, M.; Gavey, E. L.; Regier, J.; Ras Ali, Z.; Carlos, L. D.; Ferreira, R. A. S.; Pilkington, M.
Encapsulation of a [Dy(OH2)8](3+) cation: magneto-optical and theoretical studies of a caged, emissive SMM.
Chemical communications (Cambridge, England), 2016, 52, 11335-11338
7124678 CIFC19 H20 N2 O4P 1 21/n 17.791; 13.1164; 16.9526
90; 96.895; 90
1719.86Briones, John F.; Basarab, Gregory S.
Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives via the Lewis acid-catalyzed tert-amino effect reaction.
Chemical communications (Cambridge, England), 2016, 52, 8541-8544
7124679 CIFC52 H62 F12 N2 O14 P2P -113.595; 20.8235; 23.687
74.639; 84.656; 76.364
6280.5Cheng, Ming; Yao, Chenhao; Cao, Yihan; Wang, Qi; Pan, Yi; Jiang, Juli; Wang, Leyong
4-Methylcoumarin-bridged fluorescent responsive cryptand: from [2+2] photodimerization to supramolecular polymer.
Chemical communications (Cambridge, England), 2016, 52, 8715-8718
7124680 CIFC26 H24 N2 O3P 1 21/n 19.1828; 9.0675; 26.107
90; 91.376; 90
2173.2An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124681 CIFC26 H24 N2 O3C 1 2/c 138.327; 12.158; 9.715
90; 95.51; 90
4506An, Yuanyuan; Xia, Hongguang; Wu, Jie
Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations.
Chemical communications (Cambridge, England), 2016, 52, 10415-10418
7124682 CIFC66 H57 Ce F15 N3 O2 P2 S6 Si3P -113.5981; 14.8764; 21.2531
75.799; 87.413; 75.372
4032.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124683 CIFC48 H69 Ce F15 N9 Si3C 1 2/c 123.8; 12.7595; 40.727
90; 97.599; 90
12259.2Yin, Haolin; Carroll, Patrick J.; Schelter, Eric J.
Reactions of a cerium(iii) amide with heteroallenes: insertion, silyl-migration and de-insertion.
Chemical communications (Cambridge, England), 2016, 52, 9813-9816
7124684 CIFC21 H16 OP 1 21/c 113.33; 15.13; 7.59
90; 100.77; 90
1504Jin, Ruiwen; Chen, Yiyong; Liu, Wangsheng; Xu, Dawen; Li, Yawei; Ding, Aishun; Guo, Hao
Merging photoredox catalysis with Lewis acid catalysis: activation of carbon-carbon triple bonds.
Chemical communications (Cambridge, England), 2016, 52, 9909-9912
7124685 CIFC16 H14 O5P 1 21/c 18.4933; 10.7736; 14.1815
90; 92.817; 90
1296.1Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124686 CIFC16 H13 Br O5P 21 21 218.1765; 10.7366; 16.4944
90; 90; 90
1448Chen, Dong; Xu, Wen-Dan; Liu, Hao-Miao; Li, Ming-Ming; Yan, Yong-Min; Li, Xiao-Nian; Li, Yan; Cheng, Yong-Xian; Qin, Hong-Bo
Enantioselective total synthesis of (+)-Lingzhiol via tandem semipinacol rearrangement/Friedel-Crafts type cyclization.
Chemical communications (Cambridge, England), 2016, 52, 8561-8564
7124687 CIFC15 H14 N2 O3P 1 21/c 19.7836; 19.184; 7.2536
90; 110.113; 90
1278.4Alcaide, Benito; Almendros, Pedro; Cembellín, Sara; Fernández, Israel; Martínez Del Campo, Teresa
Stereoselective synthesis of strained cage compounds via gold-catalyzed allene functionalization.
Chemical communications (Cambridge, England), 2016, 52, 10265-10268
7124688 CIFC2 H4 N6 O2C 1 2/c 112.8179; 4.8463; 18.2472
90; 100.494; 90
1114.55He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124689 CIFC3 H4 N6 O4P n a 2112.7338; 9.977; 5.136
90; 90; 90
652.5He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124690 CIFC2 H4 N6 O2P 1 21 13.5852; 16.3937; 9.4278
90; 98.448; 90
548.1He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124691 CIFC2 H4 N6 O2P 1 21/n 18.0055; 6.4742; 10.7844
90; 96.224; 90
555.65He, Chunlin; Yin, Ping; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
Energetic aminated-azole assemblies from intramolecular and intermolecular N-HO and N-HN hydrogen bonds.
Chemical communications (Cambridge, England), 2016, 52, 8123-8126
7124692 CIFC H N O SP 1 21/c 115.924; 8.289; 15.498
90; 99.13; 90
2019.7Wang, Sasa; Chen, Xinzheng; Ao, Qiaoqiao; Wang, Huifei; Zhai, Hongbin
Decarboxylative Csp(3)-Csp(3) coupling for benzylation of unstable ketone enolates: synthesis of p-(acylethyl)phenols.
Chemical communications (Cambridge, England), 2016, 52, 9454-9457
7124693 CIFC22 H26 F6 N2 Rh SbP 1 21/n 112.6576; 14.5099; 13.416
90; 106.523; 90
2362.24Hou, Wei; Yang, Yaxi; Wu, Yunxiang; Feng, Huijin; Li, Yuanchao; Zhou, Bing
Rhodium(iii)-catalyzed alkylation of primary C(sp(3))-H bonds with α-diazocarbonyl compounds.
Chemical communications (Cambridge, England), 2016, 52, 9672-9675
7124694 CIFC64 H256 Co16 N64 Nb32 O205 S4 V39P n m a23.9036; 21.2261; 18.0968
90; 90; 90
9182Hu, Ju-Fang; Han, Tian; Chi, Ying-Nan; Lin, Zheng-Guo; Xu, Yan-Qing; Yang, Song; Wei, Ding; Zheng, Yan-Zhen; Hu, Chang-Wen
Sulfur-centred polyoxoniobate-based 3D organic-inorganic hybrid compound and its magnetic behavior.
Chemical communications (Cambridge, England), 2016, 52, 10846-10849
7124695 CIFC21 H30 Li N3P 1 21 110.1048; 12.9834; 15.341
90; 102.567; 90
1964.4Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124696 CIFC38 H48 Li2 O2 P2C 1 c 110.592; 18.626; 9.119
90; 95.24; 90
1791.5Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124697 CIFC24 H37 Li N4P 1 21/c 110.1275; 8.6095; 27.5008
90; 91.558; 90
2396.98Blair, V. L.; Stevens, M. A.; Thompson, C. D.
The importance of the Lewis base in lithium mediated metallation and bond cleavage reaction of allyl amines and allyl phosphines.
Chemical communications (Cambridge, England), 2016, 52, 8111-8114
7124698 CIFC51 H57 N9 O6P 1 21/c 126.8526; 13.8261; 26.9848
90; 111.812; 90
9301.3Pfletscher, Michael; Wölper, Christoph; Gutmann, Jochen S.; Mezger, Markus; Giese, Michael
A modular approach towards functional supramolecular aggregates - subtle structural differences inducing liquid crystallinity.
Chemical communications (Cambridge, England), 2016, 52, 8549-8552
7124699 CIFC25 H39 Br Co P2 SiP 1 21/n 112.1709; 14.4443; 15.9292
90; 97.855; 90
2774.1Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124700 CIFC30 H41 Br Co P2 SiP 1 21/c 111.0181; 18.0167; 15.4914
90; 98.734; 90
3039.5Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124701 CIFC25 H42 Br4 Co P2 SiP b c a17.6793; 16.195; 23.2286
90; 90; 90
6650.7Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124702 CIFC30 H42 P2 SiP 1 21/c 113.1415; 14.3471; 16.6192
90; 112.798; 90
2888.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124703 CIFC25 H40 Br2 Co P2 SiP 1 21/c 117.1233; 9.7303; 17.9002
90; 110.977; 90
2784.8Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124704 CIFC12 H32 Br4 Co N2P b c a12.3228; 13.1299; 26.5742
90; 90; 90
4299.6Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124705 CIFC30 H42 Br2 Co P2 SiP 1 21/c 117.387; 11.5644; 15.641
90; 92.891; 90
3140.9Kim, Jin; Kim, Yujeong; Sinha, Indranil; Park, Koeun; Kim, Sun Hee; Lee, Yunho
The unusual hydridicity of a cobalt bound Si-H moiety.
Chemical communications (Cambridge, England), 2016, 52, 9367-9370
7124706 CIFC62 H59 F12 N11 O11 P2 Ru3P -115.8008; 16.2412; 19.6284
107.027; 102.696; 109.127
4263.5Zhang, Biaobiao; Li, Fei; Zhang, Rong; Ma, Chengbing; Chen, Lin; Sun, Licheng
Characterization of a trinuclear ruthenium species in catalytic water oxidation by Ru(bda)(pic)2 in neutral media.
Chemical communications (Cambridge, England), 2016, 52, 8619-8622
7124707 CIFC47 H34 N6 O3P c a 2126.853; 10.1988; 27.005
90; 90; 90
7395.8Luciano, M.; Tardie, W.; Zeller, M.; Brückner, C
Supersizing pyrrole-modified porphyrins by reversal of the 'breaking and mending' strategy.
Chemical communications (Cambridge, England), 2016, 52, 10133-10136
7124708 CIFC24 H20 O3P 1 21/c 111.887; 10.4572; 14.8193
90; 100.36; 90
1812.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124709 CIFC24 H20 O4P 1 21/n 112.6203; 10.0898; 15.4768
90; 106.857; 90
1886.08Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124710 CIFC23 H16 Br2 O4P -18.0971; 11.2035; 12.1077
87.795; 71.122; 74.233
998.7Ma, Ben; Wu, Ziang; Huang, Ben; Liu, Lu; Zhang, Junliang
Gold-catalysed facile access to indene scaffolds via sequential C-H functionalization and 5-endo-dig carbocyclization.
Chemical communications (Cambridge, England), 2016, 52, 9351-9354
7124711 CIFC18 H22 Cl2 O6P c a 2112.3202; 4.6501; 32.022
90; 90; 90
1834.5Kaufmann, Lena; Kennedy, Stuart R.; Jones, Christopher D.; Steed, Jonathan W.
Cavity-containing supramolecular gels as a crystallization tool for hydrophobic pharmaceuticals.
Chemical communications (Cambridge, England), 2016, 52, 10113-10116
7124712 CIFC19 H24 N O6 P SP 319.7393; 9.7393; 18.532
90; 90; 120
1522.3Yan, Zhong; Wu, Bo; Gao, Xiang; Zhou, Yong-Gui
Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids.
Chemical communications (Cambridge, England), 2016, 52, 10882-10885
7124713 CIFC36 H41 N3 O10 S3P 6314.5223; 14.5223; 10.2703
90; 90; 120
1875.8Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124714 CIFC288 H264 Ag12 N24 O96 Re12 S24F 4 3 235.7237; 35.7237; 35.7237
90; 90; 90
45590Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124715 CIFC288 H264 Ag12 B12 F48 N24 O48 S24F 4 3 235.4548; 35.4548; 35.4548
90; 90; 90
44568.2Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124716 CIFC39 H42 N6 O12 S3R 3 :H28.138; 28.138; 4.4445
90; 90; 120
3047.5Fowler, Jonathan M.; Thorp-Greenwood, Flora L; Warriner, Stuart L.; Willans, Charlotte E.; Hardie, Michaele J.
M12L8 metallo-supramolecular cube with cyclotriguaiacylene-type ligand: spontaneous resolution of cube and its constituent host ligand.
Chemical communications (Cambridge, England), 2016, 52, 8699-8702
7124717 CIFC42.98 H46.96 Ag Cl3.96 N3 O4 PP 21 21 2114.018; 17.0222; 19.3743
90; 90; 90
4623.04de la Campa, Raquel; Gammack Yamagata, Adam D.; Ortín, Irene; Franchino, Allegra; Thompson, Amber L.; Odell, Barbara; Dixon, Darren J.
Catalytic enantio- and diastereoselective Mannich reaction of α-substituted isocyanoacetates and ketimines.
Chemical communications (Cambridge, England), 2016, 52, 10632-10635
7124718 CIFC28 H20 O2P 1 21 19.4569; 19.807; 21.941
90; 96.83; 90
4080.7Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124719 CIFC20 H14 O2P 3110.784; 10.784; 10.863
90; 90; 120
1094.1Zhang, Xin; Chen, Lin; Chen, Xiang-Yu; Zhang, Hanzhi; Yang, Liuqing; Yang, Fengchun
Effective separation of single-walled carbon nanotubes and their very different electrochemical behaviours.
Chemical communications (Cambridge, England), 2016, 52, 9287-9290
7124720 CIFC39 H84 Ge10 N7 O12 Rb2P -110.8759; 13.4395; 21.2985
85.907; 88.885; 88.995
3104.2Bentlohner, Manuel M.; Fischer, Christina; Fässler, Thomas F
Synthesis and characterization of pristine closo-[Ge10](2.).
Chemical communications (Cambridge, England), 2016, 52, 9841-9843
7124721 CIFC38 H32 N4 O2P 1 21/n 111.4777; 15.9325; 17.0968
90; 103.233; 90
3043.4Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124722 CIFC46 H32 D8 N4 O3P -19.7141; 13.7175; 13.8642
92.206; 97.198; 98.744
1808.46Krick, Marcel; Holstein, Julian; Würtele, Christian; Clever, Guido H.
Endohedral dynamics of push-pull rotor-functionalized cages.
Chemical communications (Cambridge, England), 2016, 52, 10411-10414
7124723 CIFC40 H43 Br6 N9 P2P 1 21/c 115.79; 17.796; 16.457
90; 104.672; 90
4473.6Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124724 CIFC84 H93.9 Br2 F24 N19.05 O0.47 P2 Sb4P -112.1048; 13.7318; 16.1379
108.884; 98.2298; 102.753
2407.61Đorđević, Nemanja; Ganguly, Rakesh; Petković, Milena; Vidović, Dragoslav
Bis(carbodicarbene)phosphenium trication: the case against hypervalency.
Chemical communications (Cambridge, England), 2016, 52, 9789-9792
7124725 CIFC38 H26 F2P -19.3318; 16.3035; 18.6019
94.673; 90.768; 100.362
2773.6Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124726 CIFC37 H28 Cl2 N2P 1 21/n 110.2875; 9.5469; 30.516
90; 90.739; 90
2996.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124727 CIFC40 H32 S2P 1 21/c 19.6317; 9.5173; 33.0419
90; 96.269; 90
3010.8Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124728 CIFC40 H32 S2P 1 21/c 116.2653; 11.5962; 18.2995
90; 115.9; 90
3104.9Zhuang, Zeyan; Shen, Pingchuan; Ding, Siyang; Luo, Wenwen; He, Bairong; Nie, Han; Wang, Bohan; Huang, Tianbai; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
Synthesis, aggregation-enhanced emission, polymorphism and piezochromism of TPE-cored foldamers with through-space conjugation.
Chemical communications (Cambridge, England), 2016, 52, 10842-10845
7124729 CIFC35 H36 Br Cl4 Ir N2P 1 21/n 111.5187; 12.8279; 23.1283
90; 96.529; 90
3395.29Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124730 CIFC41 H36 Br Ir N2P 21 21 2113.7643; 14.1122; 16.9238
90; 90; 90
3287.4Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124731 CIFC33 H32 Br Ir N2P 21 21 219.2873; 16.9087; 17.495
90; 90; 90
2747.3Hellou, Nora; Jahier-Diallo, Claire; Baslé, Olivier; Srebro-Hooper, Monika; Toupet, Loïc; Roisnel, Thierry; Caytan, Elsa; Roussel, Christian; Vanthuyne, Nicolas; Autschbach, Jochen; Mauduit, Marc; Crassous, Jeanne
Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.
Chemical communications (Cambridge, England), 2016, 52, 9243-9246
7124732 CIFC20 H20 N2 O2P 1 21/n 19.797; 9.3477; 19.3037
90; 103.385; 90
1719.8Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124733 CIFC19 H19 N3 O2P 1 21/c 17.9685; 10.0372; 20.628
90; 91.778; 90
1649.1Kim, Won Young; Shi, Hu; Jung, Hyo Sung; Cho, Daeheum; Verwilst, Peter; Lee, Jin Yong; Kim, Jong Seung
Coumarin-decorated Schiff base hydrolysis as an efficient driving force for the fluorescence detection of water in organic solvents.
Chemical communications (Cambridge, England), 2016, 52, 8675-8678
7124734 CIFC14 H14 F N O3P 21 21 218.2754; 12.082; 13.332
90; 90; 90
1333Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124735 CIFC17 H19 N O4P 1 21/n 114.349; 7.2477; 14.692
90; 105.12; 90
1475Liu, Jianchao; Xu, Xiaobing; Li, Jiuyi; Liu, Bo; Jiang, Huanfeng; Yin, Biaolin
Palladium-catalyzed dearomatizing 2,5-alkoxyarylation of furan rings: diastereospecific access to spirooxindoles.
Chemical communications (Cambridge, England), 2016, 52, 9550-9553
7124736 CIFC14 H12 N2 O2P -16.0661; 7.8841; 12.8564
91.07; 94.098; 97.33
608.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124737 CIFC16 H16 N2 O2P -19.2837; 9.9699; 9.9836
92.401; 112.162; 116.147
743.75Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124738 CIFC18 H16 N2 O2 SP 1 21/c 18.4209; 28.5775; 6.9049
90; 101.544; 90
1628.04Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124739 CIFC18 H17 N O4 SP -16.5556; 11.4813; 12.6356
113.781; 98.198; 93.092
854.85Singh, RahulKumar Rajmani; Pawar, Samir Kundlik; Huang, Min-Jie; Liu, Rai-Shung
Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes.
Chemical communications (Cambridge, England), 2016, 52, 11434-11437
7124740 CIFC162 H66 Cl8 N2 O14P -116.2768; 16.3003; 23.6077
94.242; 95.588; 115.579
5575.6Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784
7124741 CIFC156 H51 Cl8 O12P -113.8208; 17.4812; 24.2884
76.082; 87.204; 70.991
5382.5Hisaki, Ichiro; Nakagawa, Shoichi; Sato, Hiroyasu; Tohnai, Norimitsu
Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds.
Chemical communications (Cambridge, England), 2016, 52, 9781-9784

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