Crystallography Open Database

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7121564 CIFC30 H31 F2 N O4 SP -113.8373; 14.6324; 16.7936
65.506; 85.068; 61.827		2702Li, Ming; Wang, Cui-Tian; Qiu, Yi-Feng; Zhu, Xin-Yu; Han, Ya-Ping; Xia, Yu; Li, Xue-Song; Liang, Yong-Min
Base promoted direct difunctionalization/cascade cyclization of 1,6-enynes.
Chemical communications (Cambridge, England), 2018, 54, 5334-5337
7121565 CIFC31 H33 F2 N O5 SP 1 21/n 112.5836; 13.0599; 17.6689
90; 91.349; 90		2902.91Li, Ming; Wang, Cui-Tian; Qiu, Yi-Feng; Zhu, Xin-Yu; Han, Ya-Ping; Xia, Yu; Li, Xue-Song; Liang, Yong-Min
Base promoted direct difunctionalization/cascade cyclization of 1,6-enynes.
Chemical communications (Cambridge, England), 2018, 54, 5334-5337
7121566 CIFC26 H26 F6 N5 O P PdP -16.5861; 12.6581; 17.131
109.005; 99.386; 92.908		1323.96Zou, Chao; Lin, Jinqiang; Suo, Sa; Xie, Mo; Chang, Xiaoyong; Lu, Wei
Palladium(ii) N-heterocyclic allenylidene complexes with extended intercationic PdPd interactions and MMLCT phosphorescence.
Chemical communications (Cambridge, England), 2018, 54, 5319-5322
7121567 CIFC23 H19 F6 N4 P PdP -18.2664; 11.968; 12.4012
73.332; 73.511; 74.085		1101.9Zou, Chao; Lin, Jinqiang; Suo, Sa; Xie, Mo; Chang, Xiaoyong; Lu, Wei
Palladium(ii) N-heterocyclic allenylidene complexes with extended intercationic PdPd interactions and MMLCT phosphorescence.
Chemical communications (Cambridge, England), 2018, 54, 5319-5322
7121568 CIFC36 H48 Cl4 Cu2 N8 O2 S2P 1 21/c 18.8724; 13.043; 17.77
90; 95.506; 90		2046.9Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121569 CIFC35.78 H45.44 Cl4 Cu2 N8 O0.47P 1 21/c 18.6706; 13.3945; 18.2327
90; 95.236; 90		2108.7Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121570 CIFC40 H52 Cl4 Cu2 N8 O2P 1 21/c 18.8606; 13.145; 18.08
90; 95.808; 90		2095Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121571 CIFC38 H48 Cl4 Cu2 N8 O2P 1 21/c 18.755; 13.3722; 17.687
90; 95.982; 90		2059.4Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121572 CIFC36 H42 Cl4 Cu2 N10P 1 21/c 18.5707; 12.8298; 18.181
90; 91.579; 90		1998.4Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121573 CIFC35.52 H44.8 Cl4 Cu2 N8 O0.88P 1 21/c 18.5758; 13.295; 17.9793
90; 95.182; 90		2041.54Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121574 CIFC36.99 H47.97 Cl4 Cu2 N8P 1 21/c 18.499; 13.247; 18.335
90; 95.452; 90		2054.9Nikolayenko, Varvara I.; van Wyk, Lisa M.; Munro, Orde Q.; Barbour, Leonard J.
Supramolecular solvatochromism: mechanistic insight from crystallography, spectroscopy and theory.
Chemical communications (Cambridge, England), 2018, 54, 6975-6978
7121575 CIFC0 H224 Mn72 Na8 O408 W48P -120.043; 20.1636; 32.173
93.914; 96.564; 104.502		12442Zhang, Chao; Zhang, Mengrui; Shi, Hongyu; Zeng, Qingdao; Zhang, Dongdi; Zhao, Yaqing; Wang, Yuan; Ma, Pengtao; Wang, Jingping; Niu, Jingyang
A high-nuclearity isopolyoxotungstate based manganese cluster: one-pot synthesis and step-by-step assembly.
Chemical communications (Cambridge, England), 2018, 54, 5458-5461
7121577 CIFC19 H31 B Fe N2 SiP 1 21/n 16.3615; 19.7152; 15.9518
90; 94.707; 90		1993.9Bhattacharjee, Hridaynath; Dey, Subhayan; Zhu, Jianfeng; Sun, Wei; Müller, Jens
Strained azabora[2]ferrocenophanes.
Chemical communications (Cambridge, England), 2018, 54, 5562-5565
7121578 CIFC25 H46 B Fe N Si3P 1 21/c 116.488; 9.3747; 18.1053
90; 95.939; 90		2783.5Bhattacharjee, Hridaynath; Dey, Subhayan; Zhu, Jianfeng; Sun, Wei; Müller, Jens
Strained azabora[2]ferrocenophanes.
Chemical communications (Cambridge, England), 2018, 54, 5562-5565
7121579 CIFC21 H33 B Fe N2P 1 21/n 16.2078; 20.601; 15.7389
90; 94.438; 90		2006.76Bhattacharjee, Hridaynath; Dey, Subhayan; Zhu, Jianfeng; Sun, Wei; Müller, Jens
Strained azabora[2]ferrocenophanes.
Chemical communications (Cambridge, England), 2018, 54, 5562-5565
7121586 CIFC66 H50 B F24 P RuP 1 21/n 113.764; 17.7878; 25.873
90; 103.531; 90		6158.7Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121587 CIFC80 H56 B F24 P RuP -112.285; 15.887; 18.76
86.105; 79.344; 84.218		3575Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121588 CIFC68 H54 B F24 P RuP -112.9248; 13.019; 19.015
82.752; 84.077; 84.036		3143.7Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121589 CIFC77 H54 B F24 O P RuP -112.7071; 15.3471; 19.473
111.924; 92.508; 99.722		3448.6Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121590 CIFC76 H54 B F24 P RuP 1 21/c 118.038; 19.73; 19.271
90; 95.329; 90		6829Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121591 CIFC70 H52 B F24 P RuP -117.512; 19.924; 21.061
109.815; 93.484; 110.481		6340.7Kuwabara, Takuya; Kato, Takahiro; Takano, Kouichi; Kodama, Shintaro; Manabe, Yuuka; Tsuchida, Noriko; Takano, Keiko; Minami, Yasunori; Hiyama, Tamejiro; Ishii, Youichi
P-C reductive elimination in Ru(ii) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles.
Chemical communications (Cambridge, England), 2018, 54, 5357-5360
7121592 CIFC15 H13 N3 OP 1 21/c 112.9903; 7.8379; 13.2745
90; 114.935; 90		1225.58Croix, C.; Massip, S.; Viaud-Massuard, M-C
Synthesis of naphthyridin-2(1H)-one derivatives via ring expansion of 3-substituted-1H-pyrrolo[2,3-b]pyridin-2(3H)-one derivatives.
Chemical communications (Cambridge, England), 2018, 54, 5538-5541
7121593 CIFC61.5 H53.5 Cl4.5 N12 O4P -110.8247; 14.6849; 19.4686
74.323; 82.323; 77.013		2894.6Croix, C.; Massip, S.; Viaud-Massuard, M-C
Synthesis of naphthyridin-2(1H)-one derivatives via ring expansion of 3-substituted-1H-pyrrolo[2,3-b]pyridin-2(3H)-one derivatives.
Chemical communications (Cambridge, England), 2018, 54, 5538-5541
7121594 CIFC15 H18 N2 OC 1 2/m 120.1725; 7.0286; 8.788
90; 92.475; 90		1244.84Wu, Wanqing; Li, Meng; Zheng, Jia; Hu, Weigao; Li, Chunsheng; Jiang, Huanfeng
Tandem cyclization of o-alkynylanilines with isocyanides triggered by intramolecular nucleopalladation: access to heterocyclic fused 2-aminoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 6855-6858
7121595 CIFC4 H10 Cr N6 O8 P2P 1 21/c 115.303; 8.7095; 9.695
90; 91.626; 90		1291.6Ohara, Yuki; Hinokimoto, Akira; Chen, Wenqian; Kitao, Takashi; Nishiyama, Yusuke; Hong, You-Lee; Kitagawa, Susumu; Horike, Satoshi
Formation of coordination polymer glass by mechanical milling: dependence on metal ions and molecular doping for H<sup>+</sup> conductivity.
Chemical communications (Cambridge, England), 2018, 54, 6859-6862
7121596 CIFC2 H5 Fe0.5 N3 O4 PP b c n8.603; 9.609; 15.328
90; 90; 90		1267.1Ohara, Yuki; Hinokimoto, Akira; Chen, Wenqian; Kitao, Takashi; Nishiyama, Yusuke; Hong, You-Lee; Kitagawa, Susumu; Horike, Satoshi
Formation of coordination polymer glass by mechanical milling: dependence on metal ions and molecular doping for H<sup>+</sup> conductivity.
Chemical communications (Cambridge, England), 2018, 54, 6859-6862
7121597 CIFC2 H5 Mn0.5 N3 O4 PP b c n8.708; 9.681; 15.573
90; 90; 90		1312.8Ohara, Yuki; Hinokimoto, Akira; Chen, Wenqian; Kitao, Takashi; Nishiyama, Yusuke; Hong, You-Lee; Kitagawa, Susumu; Horike, Satoshi
Formation of coordination polymer glass by mechanical milling: dependence on metal ions and molecular doping for H<sup>+</sup> conductivity.
Chemical communications (Cambridge, England), 2018, 54, 6859-6862
7121598 CIFC2 H5 Co0.5 N3 O4 PP b c n8.477; 9.531; 15.479
90; 90; 90		1250.6Ohara, Yuki; Hinokimoto, Akira; Chen, Wenqian; Kitao, Takashi; Nishiyama, Yusuke; Hong, You-Lee; Kitagawa, Susumu; Horike, Satoshi
Formation of coordination polymer glass by mechanical milling: dependence on metal ions and molecular doping for H<sup>+</sup> conductivity.
Chemical communications (Cambridge, England), 2018, 54, 6859-6862
7121599 CIFC22 H26 O5P 1 21 17.0443; 24.124; 11.1252
90; 99.194; 90		1866.29Qiu, Yuanyou; Zhong, Jiaxin; Du, Shan; Gao, Shuanhu
Synthetic studies on daphniglaucins.
Chemical communications (Cambridge, England), 2018, 54, 5554-5557
7121600 CIFC24 H34 O3C 1 2/c 120.658; 8.0271; 26.312
90; 103.436; 90		4243.7Qiu, Yuanyou; Zhong, Jiaxin; Du, Shan; Gao, Shuanhu
Synthetic studies on daphniglaucins.
Chemical communications (Cambridge, England), 2018, 54, 5554-5557
7121601 CIFC32 H42 O4P -19.552; 13.723; 21.581
100.389; 93.85; 90.376		2775.7Qiu, Yuanyou; Zhong, Jiaxin; Du, Shan; Gao, Shuanhu
Synthetic studies on daphniglaucins.
Chemical communications (Cambridge, England), 2018, 54, 5554-5557
7121602 CIFC27 H21 Mo O6 PP -19.6734; 10.6787; 12.9836
76.188; 83.221; 73.4935		1246.92Kyri, A. W.; Gleim, F.; García Alcaraz, A; Schnakenburg, G.; Espinosa Ferao, A.; Streubel, R.
"Low-coordinate" 1,2-oxaphosphetanes - a new opportunity in coordination and main group chemistry.
Chemical communications (Cambridge, England), 2018, 54, 7123-7126
7121603 CIFC22 H21 Au Cl O PP 1 21/c 18.3743; 7.4432; 31.6312
90; 96.768; 90		1957.88Kyri, A. W.; Gleim, F.; García Alcaraz, A; Schnakenburg, G.; Espinosa Ferao, A.; Streubel, R.
"Low-coordinate" 1,2-oxaphosphetanes - a new opportunity in coordination and main group chemistry.
Chemical communications (Cambridge, England), 2018, 54, 7123-7126
7121604 CIFC22 H21 O PP 1 21 18.3304; 25.6709; 9.0341
90; 115.043; 90		1750.31Kyri, A. W.; Gleim, F.; García Alcaraz, A; Schnakenburg, G.; Espinosa Ferao, A.; Streubel, R.
"Low-coordinate" 1,2-oxaphosphetanes - a new opportunity in coordination and main group chemistry.
Chemical communications (Cambridge, England), 2018, 54, 7123-7126
7121605 CIFC51 H59 Cl Cu2 N17 O17P n n m16.418; 29.213; 14.052
90; 90; 90		6740Wu, Xue-Song; Wang, Xin-Long; Zhu, Fu-Long; Bao, Hong-Fei; Qin, Chao; Su, Zhong-Min
Guest exchange in a porous cucurbit[6]uril-based metal-organic rotaxane framework probed by NMR and X-ray crystallography.
Chemical communications (Cambridge, England), 2018, 54, 5474-5477
7121606 CIFC57 H49 Cl Cu2 N14 O14P n n m16.261; 29.33; 14.304
90; 90; 90		6822Wu, Xue-Song; Wang, Xin-Long; Zhu, Fu-Long; Bao, Hong-Fei; Qin, Chao; Su, Zhong-Min
Guest exchange in a porous cucurbit[6]uril-based metal-organic rotaxane framework probed by NMR and X-ray crystallography.
Chemical communications (Cambridge, England), 2018, 54, 5474-5477
7121607 CIFC18 H13 NF d d 212.7887; 38.195; 10.823
90; 90; 90		5286.7Zhang, Kai; Sun, Qikun; Zhang, Zhenzhen; Tang, Linagliang; Xie, Zongliang; Chi, Zhenguo; Xue, Shanfeng; Zhang, Haichang; Yang, Wenjun
Touch-sensitive mechanoluminescence crystals comprising a simple purely organic molecule emit bright blue fluorescence regardless of crystallization methods.
Chemical communications (Cambridge, England), 2018, 54, 5225-5228
7121608 CIFC20 H15 Br F3 N O4P 21 21 217.0842; 14.2629; 18.9648
90; 90; 90		1916.23Kondo, Hiroya; Maeno, Mayaka; Hirano, Kazuki; Shibata, Norio
Asymmetric synthesis of α-trifluoromethoxy ketones with a tetrasubstituted α-stereogenic centre via the palladium-catalyzed decarboxylative allylic alkylation of allyl enol carbonates.
Chemical communications (Cambridge, England), 2018, 54, 5522-5525
7121609 CIFC12 H24 Cl3.5 O3 PuP 1 2/c 112.264; 11.172; 13.938
90; 104.374; 90		1849.9Pattenaude, Scott A.; Anderson, Nickolas H.; Bart, Suzanne C.; Gaunt, Andrew J.; Scott, Brian L.
Non-aqueous neptunium and plutonium redox behaviour in THF - access to a rare Np(iii) synthetic precursor.
Chemical communications (Cambridge, England), 2018, 54, 6113-6116
7121610 CIFC28 H40 Cl3 N4 Np O2C 1 2/c 112.5752; 15.7756; 15.1347
90; 108.711; 90		2843.8Pattenaude, Scott A.; Anderson, Nickolas H.; Bart, Suzanne C.; Gaunt, Andrew J.; Scott, Brian L.
Non-aqueous neptunium and plutonium redox behaviour in THF - access to a rare Np(iii) synthetic precursor.
Chemical communications (Cambridge, England), 2018, 54, 6113-6116
7121611 CIFC12 H24 Cl4 Np O3P 1 21 17.8064; 14.381; 8.4636
90; 100.837; 90		933.2Pattenaude, Scott A.; Anderson, Nickolas H.; Bart, Suzanne C.; Gaunt, Andrew J.; Scott, Brian L.
Non-aqueous neptunium and plutonium redox behaviour in THF - access to a rare Np(iii) synthetic precursor.
Chemical communications (Cambridge, England), 2018, 54, 6113-6116
7121612 CIFC30 H44 O ZrP 1 21/n 18.6735; 32.9368; 9.8794
90; 110.658; 90		2640.9Jian, Zhongbao; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Zirconocene mediated acetylboron chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5724-5727
7121613 CIFC49 H57 B F10 O3 ZrC 1 2/c 126.8923; 10.9665; 31.0978
90; 94.806; 90		9138.9Jian, Zhongbao; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Zirconocene mediated acetylboron chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5724-5727
7121614 CIFC44 H47 B F10 O2 ZrP -112.4315; 17.3708; 21.1666
110.538; 104.768; 97.356		4017.8Jian, Zhongbao; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Zirconocene mediated acetylboron chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5724-5727
7121615 CIFC43 H45 B F10 O2 ZrP -19.9866; 13.5663; 17.4676
71.19; 82.82; 69.877		2103.13Jian, Zhongbao; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Zirconocene mediated acetylboron chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5724-5727
7121617 CIFC24 H25 N O3 SP 18.3029; 10.9797; 12.3088
77.695; 82.174; 84.301		1083.25Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121618 CIFC24 H23 Cl2 N O3 SP 1 21 19.0371; 8.0682; 16.2367
90; 103.107; 90		1153.03Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121619 CIFC18 H19 N O3 SP 1 21/n 111.26646; 6.7203; 21.0219
90; 101.248; 90		1561.08Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121620 CIFC28 H27 N O3 SP 21 21 218.2814; 12.1086; 23.3936
90; 90; 90		2345.8Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121621 CIFC26 H27 N O3 SP 1 21 112.3854; 8.06169; 23.0268
90; 94.441; 90		2292.26Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121622 CIFC23.5 H26.5 N O3 S2P 1 21 115.72773; 8.01122; 18.9065
90; 111.479; 90		2216.75Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121623 CIFC25 H27 N O3 SP 21 21 217.977; 15.2993; 18.0186
90; 90; 90		2199Nguyen, Thi Le Nhon; Incerti-Pradillos, Celia A; Lewis, William; Lam, Hon Wai
Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations.
Chemical communications (Cambridge, England), 2018, 54, 5622-5625
7121624 CIFC70 H76 Ag Au2 Cl N2 O3 P2P -113.8956; 16.1336; 16.6738
78.941; 78.141; 65.151		3296.1Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121625 CIFC64 H64 Au2 Br Cu N2 O P2P 1 21/c 118.6441; 14.8478; 24.59
90; 107.238; 90		6501.3Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121626 CIFC82 H79 Au3 Cl0.25 N2 O P3P 1 21/c 113.9827; 14.8116; 36.774
90; 90.166; 90		7616.1Zhang, Fan; Cao, Xiao-Ming; Wang, Jiwei; Jiao, Jiajun; Huang, Yongming; Shi, Min; Braunstein, Pierre; Zhang, Jun
A tritopic carbanionic N-heterocyclic dicarbene and its homo- and heterometallic coinage metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 5736-5739
7121627 CIFC12 H12 O3P -16.7868; 8.5848; 9.4383
87.679; 83.576; 73.938		525.1Shen, Guo; Zhou, Wen-Jun; Zhang, Xiao-Bo; Cao, Guang-Mei; Zhang, Zhen; Ye, Jian-Heng; Liao, Li-Li; Li, Jing; Yu, Da-Gang
Synthesis of tetronic acids from propargylic alcohols and CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 5610-5613
7121628 CIFC20 H16 N2P 1 21/n 111.883; 6.3386; 20.211
90; 92.61; 90		1520.7Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121629 CIFC32 H22 N2 O4 ZnP 1 21/n 110.553; 13.677; 17.241
90; 93.47; 90		2483.9Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121630 CIFC36 H22 N2 O8 Zn2P -110.502; 11.871; 13.571
94.67; 108.33; 104.03		1535.1Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121631 CIFC36 H22 N2 O8 Zn2P -110.324; 12.009; 13.22
94.44; 111.17; 97.2		1503Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121632 CIFC32 H22 N2 O4 ZnP 1 21/n 110.923; 13.139; 17.004
90; 94.47; 90		2432.9Li, Ni-Ya; Liu, Dong; Abrahams, Brendan F.; Lang, Jian-Ping
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 5831-5834
7121633 CIFC22 H28 O4P 659.0951; 9.0951; 38.8243
90; 90; 120		2781.31Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121634 CIFC20 H24 O4C 1 2/c 140.9654; 8.6677; 9.9042
90; 102.185; 90		3437.51Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121635 CIFC19 H22 O4P b c n7.4984; 10.1051; 20.5483
90; 90; 90		1556.99Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121636 CIFC17 H18 O4C 1 2/c 111.1202; 11.2585; 11.2577
90; 99.472; 90		1390.21Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121637 CIFC18 H20 O4P c a 2148.377; 7.5624; 21.0775
90; 90; 90		7711.1Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121638 CIFC21 H26 O4P -110.9041; 11.813; 15.392
67.718; 79.863; 89.142		1803.04Ivanova, Lena V.; Navale, Tushar S.; Wang, Denan; Lindeman, Sergey; Ivanov, Maxim V.; Rathore, Rajendra
Towards the rational design of novel charge-transfer materials: biaryls with a dihedral angle-independent hole delocalization mechanism.
Chemical communications (Cambridge, England), 2018, 54, 5851-5854
7121639 CIFC24 H0 In3 O15C m c m21.892; 37.916; 7.257
90; 90; 90		6024Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121640 CIFC24 H12 In3 O15C m c m21.851; 37.882; 7.246
90; 90; 90		5998Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121641 CIFC24 H12 In3 O15C m c m21.884; 37.906; 7.253
90; 90; 90		6017Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121642 CIFC24 H12 In3 O15C m c m21.841; 37.87; 7.246
90; 90; 90		5993Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121643 CIFC24 H12 In3 O15C m c m21.86; 37.89; 7.248
90; 90; 90		6003Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121644 CIFC24 H12 In3 O15C m c m21.872; 37.897; 7.25
90; 90; 90		6009Liu, Zhanning; Li, Qiang; Zhu, He; Lin, Kun; Deng, Jinxia; Chen, Jun; Xing, Xianran
3D negative thermal expansion in orthorhombic MIL-68(In).
Chemical communications (Cambridge, England), 2018, 54, 5712-5715
7121645 CIFC30 H45 Cl6 N2 P Pt RuP -110.0388; 11.4072; 15.5551
92.9312; 90.6096; 94.4168		1773.48Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121646 CIFC28 H53 Cl2 N2 O5 P PtP -19.4929; 13.9948; 14.1277
110.137; 105.007; 92.6871		1682.79Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121647 CIFC28 H45 Cl2 N2 O P PtP -19.674; 10.329; 15.976
90.696; 106.253; 99.069		1510.7Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121648 CIFC44 H81 Cl4 O P3 Pt RuP 1 21/n 115.8062; 16.5261; 19.3331
90; 91.648; 90		5048Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121649 CIFC79 H98 B Cl2 N3 P2 Pt RuP -112.9504; 14.9184; 20.154
104.998; 99.652; 97.274		3648.3Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121650 CIFC51 H44 Cl4 P4 Pt RuC 1 2/c 118.9; 21.5155; 16.337
90; 120.935; 90		5698.3Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121651 CIFC51.5 H75.5 Cl21.5 N P2 RuP 1 21/c 116.7297; 19.5656; 21.1868
90; 94.149; 90		6916.8Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121652 CIFC54 H96.5 Cl4 N1.5 P4 Pt RuP 1 21/c 114.6472; 19.8469; 21.394
90; 97.1342; 90		6171.1Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121653 CIFC28 H46 Cl13 N4 O P Pt RuP 1 21/n 114.4348; 11.4929; 27.5886
90; 104.657; 90		4427.9Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121654 CIFC56.33 H80.33 Cl7.33 N3 P2 Pt RuP -328.4392; 28.4392; 13.8884
90; 90; 120		9727.9Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121655 CIFC55.16 H52.08 Cl5.23 N O0.38 P4 Pt RuP -113.1006; 13.1671; 18.1048
72.0661; 72.0477; 63.5052		2605.1Reinholdt, Anders; Hill, Anthony F.; Bendix, Jesper
Synthons for carbide complex chemistry.
Chemical communications (Cambridge, England), 2018, 54, 5708-5711
7121656 CIFC100 H60 B12 F60 N O12P -113.3889; 13.8983; 29.7778
97.621; 100.29; 93.583		5382.7Wixtrom, Alex I.; Parvez, Zeeshan A.; Savage, Miles D.; Qian, Elaine A.; Jung, Dahee; Khan, Saeed I.; Rheingold, Arnold L.; Spokoyny, Alexander M.
Tuning the electrochemical potential of perfunctionalized dodecaborate clusters through vertex differentiation.
Chemical communications (Cambridge, England), 2018, 54, 5867-5870
7121657 CIFC93 H58 B12 F55 N2 O13P -114.125; 27.2616; 29.4644
110.44; 91.699; 97.139		10516.5Wixtrom, Alex I.; Parvez, Zeeshan A.; Savage, Miles D.; Qian, Elaine A.; Jung, Dahee; Khan, Saeed I.; Rheingold, Arnold L.; Spokoyny, Alexander M.
Tuning the electrochemical potential of perfunctionalized dodecaborate clusters through vertex differentiation.
Chemical communications (Cambridge, England), 2018, 54, 5867-5870
7121658 CIFC52 H39 B F15 O2 PP 1 21/n 113.04; 17.682; 20.467
90; 99.613; 90		4653Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121659 CIFC34.67 H25.33 B0.67 Br0.67 F10 O1.33 P0.67P -112.6688; 18.7187; 20.0531
90.811; 91.169; 97.947		4708.1Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121660 CIFC35.33 H27.33 B0.67 F10 O1.33 P0.67P 1 21/c 112.4203; 20.1153; 18.9334
90; 97.534; 90		4689.4Liu, Liu Leo; Cao, Levy L.; Zhu, Diya; Zhou, Jiliang; Stephan, Douglas W.
Homolytic cleavage of peroxide bonds via a single electron transfer of a frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 7431-7434
7121661 CIFC56 H63 F18 N8 P3 RuI -424.9906; 24.9906; 20.6467
90; 90; 90		12894.5Rota Martir, Diego; Cordes, David B.; Slawin, Alexandra M. Z.; Escudero, Daniel; Jacquemin, Denis; Warriner, Stuart L.; Zysman-Colman, Eli
A luminescent [Pd<sub>4</sub>Ru<sub>8</sub>]<sup>24+</sup> supramolecular cage.
Chemical communications (Cambridge, England), 2018, 54, 6016-6019
7121662 CIFC448 H496 F144 N64 P24 Pd4 Ru8P 4/m n c26.7344; 26.7344; 51.852
90; 90; 90		37060Rota Martir, Diego; Cordes, David B.; Slawin, Alexandra M. Z.; Escudero, Daniel; Jacquemin, Denis; Warriner, Stuart L.; Zysman-Colman, Eli
A luminescent [Pd<sub>4</sub>Ru<sub>8</sub>]<sup>24+</sup> supramolecular cage.
Chemical communications (Cambridge, England), 2018, 54, 6016-6019
7121663 CIFC50 H54 Cl2 O2 P4 Rh2 Si2P 21 21 2113.6107; 19.3024; 19.5658
90; 90; 90		5140.3Newland, Robert J.; Lynam, Jason M.; Mansell, Stephen M.
Small bite-angle 2-phosphinophosphinine ligands enable rhodium-catalysed hydroboration of carbonyls.
Chemical communications (Cambridge, England), 2018, 54, 5482-5485
7121664 CIFC61 H48 B F24 P2 Rh SiP -113.2396; 14.6179; 18.0412
98.298; 102.651; 110.657		3092.5Newland, Robert J.; Lynam, Jason M.; Mansell, Stephen M.
Small bite-angle 2-phosphinophosphinine ligands enable rhodium-catalysed hydroboration of carbonyls.
Chemical communications (Cambridge, England), 2018, 54, 5482-5485
7121665 CIFC53 H49 B F20 Mg N4 O2P 1 21 19.435; 27.598; 10.589
90; 105.636; 90		2655.2Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121666 CIFC82 H78 B2 F40 Mg2 N8 O4P 1 21/n 112.2624; 22.472; 15.7828
90; 92.505; 90		4345Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121667 CIFC40 H39 B F20 Mg N4P -112.305; 12.709; 15.464
69.721; 70.14; 83.743		2133.4Banerjee, Sumanta; Ankur, ?; Andrews, Alex; Venugopal, Ajay
A disguised hydride in a butylmagnesium cation.
Chemical communications (Cambridge, England), 2018, 54, 5788-5791
7121668 CIFC16 H9 B F2 I N O2P -18.1072; 10.316; 18.661
85.33; 85.74; 82.69		1539.6Tao, Yi-Chen; Li, Zhi-Zhou; Wang, Xue-Dong; Xiao, Lu; Fu, Hongbing; Liao, Liang-Sheng
Fluorescence/phosphorescence-conversion in self-assembled organic microcrystals.
Chemical communications (Cambridge, England), 2018, 54, 5895-5898
7121669 CIFC18 H17 Cl N2 OP -18.075; 8.096; 13.744
94.419; 104.016; 113.589		783.5Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121670 CIFC15 H15 Cl N4P 1 21/c 113.886; 14.758; 6.953
90; 102.04; 90		1394Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121671 CIFC12 H6 F6 N2 O8 Ru2P 1 21/c 114.2908; 8.8234; 15.2802
90; 101.799; 90		1886Fan, Zhoulong; Lu, Heng; Cheng, Zhen; Zhang, Ao
Ligand-promoted ruthenium-catalyzed meta C-H chlorination of arenes using N-chloro-2,10-camphorsultam.
Chemical communications (Cambridge, England), 2018, 54, 6008-6011
7121672 CIFC17 H16 Br2 Co N4 OP 1 21/c 18.8812; 17.0462; 11.8893
90; 96.1423; 90		1789.6Shee, Sujan; Ganguli, Kasturi; Jana, Kalipada; Kundu, Sabuj
Cobalt complex catalyzed atom-economical synthesis of quinoxaline, quinoline and 2-alkylaminoquinoline derivatives.
Chemical communications (Cambridge, England), 2018, 54, 6883-6886
7121673 CIFC30 H28 Br PP 1 21/c 118.8856; 8.5457; 15.9422
90; 107.321; 90		2456.24Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121674 CIFC59 H46 B F10 PP 1 2/c 122.7843; 8.4334; 27.6135
90; 113.888; 90		4851.4Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121675 CIFC42 H30 B F10 PP -111.8477; 12.3022; 14.0634
67.621; 72.281; 67.99		1725.74Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121676 CIFC47 H36 B F10 PP 1 21/n 113.0923; 11.9735; 24.9266
90; 98.327; 90		3866.32Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121677 CIFC42 H28 B F10 O2 PC 1 2/c 120.1789; 14.4682; 23.7982
90; 98.115; 90		6878.4Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121678 CIFC54 H42 B F10 PC 1 2/c 141.3837; 8.811; 24.2497
90; 96.346; 90		8788Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121679 CIFC53 H48 B F10 N2 PP -111.6758; 12.5018; 19.7217
90.855; 106.41; 104.165		2666.56Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121680 CIFC50 H40 B Cl6 F10 PP -111.5136; 14.6603; 16.4813
77.324; 70.587; 67.496		2410.36Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121681 CIFC50 H34 B F10 PP -113.3724; 14.8949; 23.4627
75.958; 83.414; 65.374		4120.83Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121682 CIFC52 H38 B F10 PP 1 21/n 114.5964; 18.8664; 15.7176
90; 104.493; 90		4190.6Li, Jun; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Selective formation of heterocyclic trans-cycloalkenes by alkyne addition to a biphenylene-based phosphane/borane frustrated Lewis pair.
Chemical communications (Cambridge, England), 2018, 54, 6344-6347
7121683 CIFC48 H144 B12 Er2 P6P 1 21/n 114.7928; 12.1704; 24.504
90; 91.557; 90		4409.9Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121684 CIFC52 H154 B12 O P6 U2P 1 21/n 115.0395; 12.0078; 24.766
90; 90.114; 90		4472.5Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121685 CIFC52 H154 B12 Nd2 O P6P 1 21/n 115.0204; 11.9884; 24.771
90; 90.05; 90		4460.5Blake, Anastasia V.; Fetrow, Taylor V.; Theiler, Zachary J.; Vlaisavljevich, Bess; Daly, Scott R.
Homoleptic uranium and lanthanide phosphinodiboranates.
Chemical communications (Cambridge, England), 2018, 54, 5602-5605
7121686 CIFC23 H26 F N O2 SP -18.7586; 12.203; 19.973
91.534; 96.604; 90.138		2119.8Zhu, Xin-Qi; Sun, Qing; Zhang, Zhi-Xin; Zhou, Bo; Xie, Pei-Xi; Shen, Wen-Bo; Lu, Xin; Zhou, Jin-Mei; Ye, Long-Wu
Zinc-catalyzed reaction of isoxazoles with thioynol ethers involving an unprecedented 1,2-sulfur migration.
Chemical communications (Cambridge, England), 2018, 54, 7435-7438
7121687 CIFC40 H54 B4 O8P 1 21/n 112.331; 10.794; 15.681
90; 109.944; 90		1962Wakchaure, Vivek C.; Ranjeesh, Kayaramkodath C.; Goudappagouda, ?; Das, Tamal; Vanka, Kumar; Gonnade, Rajesh; Babu, Sukumaran S.
Mechano-responsive room temperature luminescence variations of boron conjugated pyrene in air.
Chemical communications (Cambridge, England), 2018, 54, 6028-6031
7121688 CIFC336 H Np24 O184F m -3 m27.6042; 27.6042; 27.6042
90; 90; 90		21034.2Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121689 CIFC22 H22 N2 Np O10C 1 2/c 115.345; 11.4621; 13.3406
90; 101.43; 90		2299.89Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121690 CIFC168 O70 Th12F m -3 m27.9879; 27.9879; 27.9879
90; 90; 90		21923.6Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121691 CIFC168 O70 Th12F m -3 m27.996; 27.996; 27.996
90; 90; 90		21943Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121692 CIFC192 Np12 O76F m -3 m33.3917; 33.3917; 33.3917
90; 90; 90		37231.9Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121693 CIFC168 Np12 O86F m -3 m27.5467; 27.5467; 27.5467
90; 90; 90		20903Martin, N. P.; März, J; Feuchter, H.; Duval, S.; Roussel, P.; Henry, N.; Ikeda-Ohno, A; Loiseau, T.; Volkringer, C.
Synthesis and structural characterization of the first neptunium based metal-organic frameworks incorporating {Np<sub>6</sub>O<sub>8</sub>} hexanuclear clusters.
Chemical communications (Cambridge, England), 2018, 54, 6979-6982
7121695 CIFC28 H20 B2 N2 S2P n a 2112.195; 12.807; 30.751
90; 90; 90		4803Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121696 CIFC28 H20 B2 N2 O S2P 1 21 113.257; 8.073; 13.405
90; 104.92; 90		1386.3Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121697 CIFC33 H26 B2 Cl2 N2P 21 21 217.742; 14.293; 25.54
90; 90; 90		2826.2Zhang, Jinyun; Liu, Fude; Sun, Zhe; Li, Chenglong; Zhang, Qian; Zhang, Chen; Liu, Zhiqiang; Liu, Xuguang
Synthesis, characterization and properties of aryl-fused bis-BN dihydropyrenes.
Chemical communications (Cambridge, England), 2018, 54, 8178-8181
7121698 CIFC22 H24 N2 O2P 1 21/c 114.8982; 5.9496; 21.2447
90; 97.139; 90		1868.5Zhou, Meng-Guang; Dai, Rui-Han; Tian, Shi-Kai
Nucleophilic addition of tertiary propargylic amines to arynes followed by a [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 6036-6039
7121699 CIFBa2 H3 N O6P -6 2 m6.9069; 6.9069; 3.8028
90; 90; 120		157.109Dong, Xuehua; Huang, Ling; Liu, Qingyu; Zeng, Hongmei; Lin, Zhien; Xu, Dingguo; Zou, Guohong
Perfect balance harmony in Ba<sub>2</sub>NO<sub>3</sub>(OH)<sub>3</sub>: a beryllium-free nitrate as a UV nonlinear optical material.
Chemical communications (Cambridge, England), 2018, 54, 5792-5795
7121704 CIFC74 H72 N6 O3P 21 21 2135.034; 10.393; 17.979
90; 90; 90		6546Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121705 CIFC74 H68 Cl2 N6 O PdC 1 2/c 131.021; 22.132; 29.199
90; 119.15; 90		17508Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121706 CIFC148 H136 Cl4 N12 O2 Pd2P -116.792; 23.687; 39.551
73.077; 84.189; 81.24		14848Jeon, Hae-Geun; Lee, Hyun Kyung; Lee, Seungwon; Jeong, Kyu-Sung
Foldamer-based helicate displaying reversible switching between two distinct conformers.
Chemical communications (Cambridge, England), 2018, 54, 5740-5743
7121707 CIFC23 H21 B2 F8 N O2 Pd3P -110.1815; 10.931; 11.5703
110.912; 92.099; 98.047		1185.81Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121708 CIFC46 H46 B2 F8 N O P Pd4P 1 21/c 115.662; 30.042; 9.1348
90; 90.782; 90		4297.7Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121709 CIFC28 H23 B2 F8 N Pd3P 1 21/n 110.6819; 11.6177; 21.577
90; 100.429; 90		2633.5Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121710 CIFC39.5 H34.5 B2 F8 N3.5 O Pd3P 1 21/c 118.3607; 14.2059; 15.0826
90; 102.778; 90		3836.6Sugawa, Tsuyoshi; Yamamoto, Koji; Murahashi, Tetsuro
Bimodal coordination of fused arenes to a Pd<sub>3</sub> cluster site.
Chemical communications (Cambridge, England), 2018, 54, 5875-5878
7121711 CIFC38 H56 Ge2 Ru2P -111.4301; 11.9637; 13.1386
87.895; 84.249; 88.71		1786.09Fujimori, Shiori; Mizuhata, Yoshiyuki; Tokitoh, Norihiro
Ru-Complexes of an anionic germabenzenyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 8044-8047
7121712 CIFC60 H87 Ge3 Ru3P -112.3082; 13.0253; 19.5207
74.599; 89.993; 71.829		2854.97Fujimori, Shiori; Mizuhata, Yoshiyuki; Tokitoh, Norihiro
Ru-Complexes of an anionic germabenzenyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 8044-8047
7121713 CIFC14 H18 Cu3 O15 P2P 1 21 18.872; 9.054; 13.255
90; 102.344; 90		1040.1Wang, Peng-Fei; Bao, Song-Song; Huang, Xin-Da; Akutagawa, T.; Zheng, Li-Min
Temperature controlled formation of polar copper phosphonates showing large dielectric anisotropy and a dehydration-induced switch from ferromagnetic to antiferromagnetic interactions.
Chemical communications (Cambridge, England), 2018, 54, 6276-6279
7121714 CIFC14 H12 Cu3 O12 P2P b c n22.65; 8.8845; 8.9245
90; 90; 90		1795.9Wang, Peng-Fei; Bao, Song-Song; Huang, Xin-Da; Akutagawa, T.; Zheng, Li-Min
Temperature controlled formation of polar copper phosphonates showing large dielectric anisotropy and a dehydration-induced switch from ferromagnetic to antiferromagnetic interactions.
Chemical communications (Cambridge, England), 2018, 54, 6276-6279
7121715 CIFC26 H28P 1 21/n 115.0392; 7.6824; 15.9139
90; 91.082; 90		1838.3Alonso, José M; Quiroga, Sabela; Codony, Sandra; Turcu, Andreea L.; Barniol-Xicota, Marta; Pérez, Dolores; Guitián, Enrique; Vázquez, Santiago; Peña, Diego
Palladium-catalyzed cocyclotrimerization of arynes with a pyramidalized alkene.
Chemical communications (Cambridge, England), 2018, 54, 5996-5999
7121716 CIFC35 H33 Cl3P -19.5957; 12.2865; 13.243
73.4435; 72.2898; 73.1598		1389.97Alonso, José M; Quiroga, Sabela; Codony, Sandra; Turcu, Andreea L.; Barniol-Xicota, Marta; Pérez, Dolores; Guitián, Enrique; Vázquez, Santiago; Peña, Diego
Palladium-catalyzed cocyclotrimerization of arynes with a pyramidalized alkene.
Chemical communications (Cambridge, England), 2018, 54, 5996-5999
7121717 CIFC51.2 H86.4 O71.2 Zr12P -112.5793; 15.7491; 16.7679
116.322; 93.693; 106.969		2774.1Fidelli, Athena M.; Karadeniz, Bahar; Howarth, Ashlee J.; Huskić, Igor; Germann, Luzia S.; Halasz, Ivan; Etter, Martin; Moon, Su-Young; Dinnebier, Robert E.; Stilinović, Vladimir; Farha, Omar K.; Friščić, Tomislav; UŽarević, Krunoslav
Green and rapid mechanosynthesis of high-porosity NU- and UiO-type metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 6999-7002
7121718 CIFC60 H92 N4 O36 Zr6I -416.0037; 16.0037; 16.2833
90; 90; 90		4170.5Fidelli, Athena M.; Karadeniz, Bahar; Howarth, Ashlee J.; Huskić, Igor; Germann, Luzia S.; Halasz, Ivan; Etter, Martin; Moon, Su-Young; Dinnebier, Robert E.; Stilinović, Vladimir; Farha, Omar K.; Friščić, Tomislav; UŽarević, Krunoslav
Green and rapid mechanosynthesis of high-porosity NU- and UiO-type metal-organic frameworks.
Chemical communications (Cambridge, England), 2018, 54, 6999-7002
7121725 CIFC36 H36 Cl6 N6 O10R -3 :H22.3483; 22.3483; 8.0031
90; 90; 120		3461.61Kosiorek, Sandra; Butkiewicz, Helena; Danylyuk, Oksana; Sashuk, Volodymyr
Pillar[6]pyridinium: a hexagonally shaped molecular box that selectively recognizes multicharged anionic species.
Chemical communications (Cambridge, England), 2018, 54, 6316-6319
7121726 CIFC8 H19 NP b c m4.8201; 7.003; 26.028
90; 90; 90		878.6Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121727 CIFC12 H27 NP b c m4.856; 7.056; 36.24
90; 90; 90		1241.7Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121728 CIFC4 H11 NC 1 2/c 18.0789; 15.538; 13.319
90; 98.065; 90		1655.4Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121729 CIFC5 H13 NP 1 21/n 18.933; 9.062; 15.56
90; 99.55; 90		1242Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121730 CIFC4 H11 NC 1 2/c 115.168; 8.902; 15.176
90; 90.67; 90		2049Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121731 CIFC6 H15 NC 1 c 114.348; 8.94; 17.768
90; 105.637; 90		2194.8Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121732 CIFC8 H19 NC 1 2/c 117.442; 11.612; 18.375
90; 90.08; 90		3722Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121733 CIFC6 H15 NC 1 2/c 114.527; 7.293; 14.148
90; 104.794; 90		1449.2Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121734 CIFC6 H15 NP 1 21/c 18.158; 10.492; 26.09
90; 90.156; 90		2233.1Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121735 CIFC3 H9 NP 1 21/n 17.761; 16.084; 14.231
90; 99.851; 90		1750Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121736 CIFC4 H11 NP 1 21/n 17.989; 15.32; 13.213
90; 96.29; 90		1607.4Hanke, Felix; Pugh, Chloe J.; Kay, Ellis F.; Taylor, Joshua B.; Todd, Stephen M.; Robertson, Craig M.; Slater, Benjamin J.; Steiner, Alexander
The simplest supramolecular helix.
Chemical communications (Cambridge, England), 2018, 54, 6012-6015
7121737 CIFC66 H82 B2 F4 N8 P2 PtP -110.503; 11.094; 14.692
106.564; 90.122; 95.097		1633.7Dhindsa, Jasveer S.; Maar, Ryan R.; Barbon, Stephanie M.; Olivia Avilés, María; Powell, Zachary K.; Lagugné-Labarthet, François; Gilroy, Joe B.
A π-conjugated inorganic polymer constructed from boron difluoride formazanates and platinum(ii) diynes.
Chemical communications (Cambridge, England), 2018, 54, 6899-6902
7121738 CIFC7 H6 N2P 1 21/c 17.3184; 5.7059; 15.844
90; 113.439; 90		607Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121739 CIFC7 H6 N2P 1 21/c 17.243; 5.4842; 16.0426
90; 101.797; 90		623.79Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121740 CIFC7 H6 N2P 1 21/c 17.3198; 5.5097; 16.0906
90; 102.034; 90		634.67Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121741 CIFC7 H6 N2P 1 21/c 17.2662; 5.4906; 16.0552
90; 101.835; 90		626.92Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121742 CIFC7 H6 N2P 1 21/c 17.3414; 5.5181; 16.1043
90; 102.118; 90		637.86Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121743 CIFC7 H6 N2P 1 21/c 17.3002; 5.5022; 16.0771
90; 101.968; 90		631.73Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121744 CIFC7 H6 N2P 1 21/c 17.3645; 5.5357; 16.147
90; 102.119; 90		643.6Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121745 CIFC7 H6 N2P 1 21/c 17.3455; 5.7043; 15.878
90; 113.224; 90		611.4Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121746 CIFC7 H6 N2P 1 21/c 17.2228; 5.4765; 16.0273
90; 101.74; 90		620.71Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121747 CIFC7 H6 N2P 1 21/c 17.332; 5.7057; 15.859
90; 113.341; 90		609.2Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121748 CIFC7 H6 N2P 1 21/c 17.368; 5.7105; 15.915
90; 113.088; 90		616Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121749 CIFC7 H6 N2P 1 21/c 17.2815; 5.4951; 16.0633
90; 101.903; 90		628.91Alimi, Lukman O.; van Heerden, Dewald P.; Lama, Prem; Smith, Vincent J.; Barbour, Leonard J.
Reversible thermosalience of 4-aminobenzonitrile.
Chemical communications (Cambridge, England), 2018, 54, 6208-6211
7121750 CIFC11 H7 F N2 O5 SP -18.2004; 11.919; 12.4
93.86; 93.52; 95.79		1200.2Smedley, Christopher J.; Giel, Marie-Claire; Molino, Andrew; Barrow, Andrew S.; Wilson, David J. D.; Moses, John E.
1-Bromoethene-1-sulfonyl fluoride (BESF) is another good connective hub for SuFEx click chemistry.
Chemical communications (Cambridge, England), 2018, 54, 6020-6023
7121751 CIFC27 H23 Br N2 O6P b c n16.1053; 20.5425; 16.542
90; 90; 90		5472.8Gurubrahamam, Ramani; Nagaraju, Koppanathi; Chen, Kwunmin
Organocatalytic synthesis of densely functionalized oxa-bridged 2,6-epoxybenzo[b][1,5]oxazocine heterocycles.
Chemical communications (Cambridge, England), 2018, 54, 6048-6051
7121752 CIFC26 H37 I N2P 1 21/n 19.4821; 14.8496; 17.729
90; 100.901; 90		2451.3Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121753 CIFC23 H31 B F4 N2P 1 21/c 115.5061; 15.3089; 9.2595
90; 90.915; 90		2197.75Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121754 CIFC17 H20 I N2 O0.5C 1 2 117.5096; 10.5339; 11.1338
90; 126.315; 90		1654.71Teng, Qiaoqiao; Wu, Wenqin; Duong, Hung A.; Huynh, Han Vinh
Ring-expanded N-heterocyclic carbenes as ligands in iron-catalysed cross-coupling reactions of arylmagnesium reagents and aryl chlorides.
Chemical communications (Cambridge, England), 2018, 54, 6044-6047
7121755 CIFC9 H9 I2 N O2P b c a12.08; 11.704; 16.182
90; 90; 90		2287.88Li, Jing; Lear, Martin J.; Hayashi, Yujiro
Autoinductive conversion of α,α-diiodonitroalkanes to amides and esters catalysed by iodine byproducts under O<sub>2</sub>.
Chemical communications (Cambridge, England), 2018, 54, 6360-6363
7121756 CIFC34 H56 Cl2 P2 Rh2 S2P 21 21 2114.121; 14.5253; 18.8086
90; 90; 90		3857.9Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121757 CIFC76 H70 Cl6 P4 Rh4 S4P 1 21/c 112.0429; 13.0157; 45.0034
90; 90.985; 90		7053.1Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121758 CIFC34 H56 Cl2 O2 P2 Rh2P b c a16.0812; 15.1354; 29.4358
90; 90; 90		7164.5Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121759 CIFC78 H76 Cl8 O4 P4 Rh4P -112.2267; 13.3049; 13.5035
73.906; 69.569; 68.304		1884.77Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121760 CIFC76 H72 Cl4 P4 Rh4 S4P -110.7617; 17.854; 19.459
78.973; 84.819; 78.382		3589.4Vlahopoulou, G.; Möller, S; Haak, J.; Hasche, P.; Drexler, H.-J.; Heller, D.; Beweries, T.
Synthesis of Rh(iii) thiophosphinito pincer hydrido complexes by base-free C-H bond activation at room temperature.
Chemical communications (Cambridge, England), 2018, 54, 6292-6295
7121761 CIFC21 H22 F O5 PP 21 21 218.7032; 13.2565; 18.0076
90; 90; 90		2077.61Sun, Jun; He, Fangcheng; Wang, Zhongyao; Pan, Dingwu; Zheng, Pengcheng; Mou, Chengli; Jin, Zhichao; Chi, Yonggui Robin
Carbene-catalyzed enal γ-carbon addition to α-ketophosphonates for enantioselective access to bioactive 2-pyranylphosphonates.
Chemical communications (Cambridge, England), 2018, 54, 6040-6043
7121762 CIFC17 H13 F3 OP 1 21/c 112.9659; 8.4037; 12.8931
90; 113.171; 90		1291.5Yokoo, Kazuma; Mori, Keiji
Divergent synthesis of CF<sub>3</sub>-substituted polycyclic skeletons based on control of activation site of acid catalysts.
Chemical communications (Cambridge, England), 2018, 54, 6927-6930
7121763 CIFC57 H43 B F20 N O2 PP -112.7541; 13.627; 17.1282
100.157; 95.562; 112.012		2672.94Volodarsky, Solomon; Dobrovetsky, Roman
Ambiphilic geometrically constrained phosphenium cation.
Chemical communications (Cambridge, England), 2018, 54, 6931-6934
7121764 CIFC21 H23 N O5P 21 21 217.1336; 12.7135; 20.4017
90; 90; 90		1850.3Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121765 CIFC16 H20 O5P 1 21 18.5141; 7.7265; 22.836
90; 94.095; 90		1498.4Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121766 CIFC16 H20 O4P 21 21 217.102; 8.451; 24.298
90; 90; 90		1458.3Abe, Hideki; Fujimaki, Mitsuru; Nakagawa, Eri; Kobayashi, Toyoharu; Ito, Hisanaka
Enantioselective total synthesis of sagittacin E and related natural products.
Chemical communications (Cambridge, England), 2018, 54, 6165-6168
7121767 CIFC62 H60 Cr2 N4 Ni O14P -18.831; 13.443; 13.675
118; 103.9; 92.2		1369.6Fotopoulou, Eirini; Martínez-Lillo, Jose; Siczek, Milosz; Lis, Tadeusz; Tangoulis, Vassilis; Evangelisti, Marco; Brechin, Euan K.; Milios, Constantinos J.
A [Cr<sub>2</sub>Ni] coordination polymer: slow relaxation of magnetization in quasi-one-dimensional ferromagnetic chains.
Chemical communications (Cambridge, England), 2018, 54, 6153-6156
7121768 CIFC80 H84 N6 O12 SnP 19.756; 13.413; 14.922
112.87; 100.33; 94.47		1746.4Natali, Mirco; Amati, Agnese; Demitri, Nicola; Iengo, Elisabetta
Formation of a long-lived radical pair in a Sn(iv) porphyrin-di(l-tyrosinato) conjugate driven by proton-coupled electron-transfer.
Chemical communications (Cambridge, England), 2018, 54, 6148-6152
7121769 CIFC19 H15 N O3 SP 1 21/n 117.529; 10.184; 18.2727
90; 99.753; 90		3214.81Huang, Yuanqiong; Guo, Zhonglin; Song, Hongjian; Liu, Yuxiu; Wang, Qingmin
Silver-copper co-catalyzed cascade intramolecular cyclization/desulfinamide/dehydrogenation: one-pot synthesis of substituted carbazoles.
Chemical communications (Cambridge, England), 2018, 54, 7143-7146
7121770 CIFC108 H187 Cu7 N30 O96 P4P 1 21 115.3831; 35.7449; 16.8107
90; 94.964; 90		9209Bruno, Rosaria; Marino, Nadia; Bartella, Lucia; Di Donna, Leonardo; De Munno, Giovanni; Pardo, Emilio; Armentano, Donatella
Highly efficient temperature-dependent chiral separation with a nucleotide-based coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 6356-6359
7121771 CIFC112 H172 Cu7 N31 O89 P4P 1 21 115.2378; 35.525; 16.7521
90; 95.389; 90		9028.2Bruno, Rosaria; Marino, Nadia; Bartella, Lucia; Di Donna, Leonardo; De Munno, Giovanni; Pardo, Emilio; Armentano, Donatella
Highly efficient temperature-dependent chiral separation with a nucleotide-based coordination polymer.
Chemical communications (Cambridge, England), 2018, 54, 6356-6359
7121772 CIFC32 H30 N2 O2P -17.925; 12.453; 13.592
83.497; 82.328; 88.609		1320.8Li, Feng; Hu, Peng; Sun, Mingming; Li, Chunju; Jia, Xueshun; Li, Jian
Ytterbium and silver co-catalyzed synthesis of pyrrole-fused bicyclic skeletons from enynones and isocyanides.
Chemical communications (Cambridge, England), 2018, 54, 6412-6415
7121773 CIFC30 H26 N2 O2C 1 2/c 131.48; 7.4853; 20.361
90; 104.443; 90		4646.2Li, Feng; Hu, Peng; Sun, Mingming; Li, Chunju; Jia, Xueshun; Li, Jian
Ytterbium and silver co-catalyzed synthesis of pyrrole-fused bicyclic skeletons from enynones and isocyanides.
Chemical communications (Cambridge, England), 2018, 54, 6412-6415
7121774 CIFC55.76 H31.5 D19.56 Fe4 N3 O22.22F m -3 m40.251; 40.251; 40.251
90; 90; 90		65212Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121775 CIFC56.86 H30.78 D17.44 Fe4 N3 O22.28F m -3 m40.216; 40.216; 40.216
90; 90; 90		65042Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121776 CIFC61.56 H40.32 D8.74 Fe4 N2.96 O23.3F m -3 m40.302; 40.302; 40.302
90; 90; 90		65461Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121777 CIFC34.9 Cu4 N2.71 O17.78F m -3 m39.9765; 39.9765; 39.9765
90; 90; 90		63887Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121778 CIFC50.24 H12.6 Cu4 D23.48 N1.56 O18.84F m -3 m39.942; 39.942; 39.942
90; 90; 90		63722Gosselin, Eric J.; Lorzing, Gregory R.; Trump, Benjamin A.; Brown, Craig M.; Bloch, Eric D.
Gas adsorption in an isostructural series of pillared coordination cages.
Chemical communications (Cambridge, England), 2018, 54, 6392-6395
7121779 CIFC36 H61 Dy Si2P -19.6968; 12.7898; 16.0392
71.948; 75.157; 80.771		1821.04Kilpatrick, Alexander F. R.; Guo, Fu-Sheng; Day, Benjamin M.; Mansikkamäki, Akseli; Layfield, Richard A.; Cloke, F Geoffrey N
Single-molecule magnet properties of a monometallic dysprosium pentalene complex.
Chemical communications (Cambridge, England), 2018, 54, 7085-7088
7121780 CIFC36 H61 Si2 YP -19.7114; 12.7624; 15.9778
72.103; 75.026; 80.722		1813.26Kilpatrick, Alexander F. R.; Guo, Fu-Sheng; Day, Benjamin M.; Mansikkamäki, Akseli; Layfield, Richard A.; Cloke, F Geoffrey N
Single-molecule magnet properties of a monometallic dysprosium pentalene complex.
Chemical communications (Cambridge, England), 2018, 54, 7085-7088
7121781 CIFC22 H16 Co N6 S2C 1 2/c 112.099; 11.399; 16.538
90; 99.939; 90		2246.6Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121782 CIFC22 H16 Co N6 S2C 1 2/c 112.605016; 11.467969; 19.683948
90; 92.9158; 90		2841.71Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121783 CIFC36 H26 Co F6 N6 S2C 1 2/c 123.3527; 11.5209; 13.7802
90; 108.764; 90		3510.4Wang, Shi-Qiang; Yang, Qing-Yuan; Mukherjee, Soumya; O'Nolan, Daniel; Patyk-Kaźmierczak, Ewa; Chen, Kai-Jie; Shivanna, Mohana; Murray, Claire; Tang, Chiu C.; Zaworotko, Michael J.
Recyclable switching between nonporous and porous phases of a square lattice (sql) topology coordination network.
Chemical communications (Cambridge, England), 2018, 54, 7042-7045
7121784 CIFC29 H21 N O3P -19.7087; 10.8041; 11.9237
78.551; 66.373; 74.278		1097.26Zheng, Zhong; Wang, Ye; Xu, Murong; Kong, Lingkai; Wang, Mengdan; Li, Yanzhong
Transition-metal-free insertion reactions of alkynes into the C-N σ-bonds of imides: synthesis of substituted enamides or chromones.
Chemical communications (Cambridge, England), 2018, 54, 6192-6195
7121785 CIFC29 H18 F N O3P 1 2/n 17.5691; 11.0082; 26.381
90; 93.532; 90		2193.9Zheng, Zhong; Wang, Ye; Xu, Murong; Kong, Lingkai; Wang, Mengdan; Li, Yanzhong
Transition-metal-free insertion reactions of alkynes into the C-N σ-bonds of imides: synthesis of substituted enamides or chromones.
Chemical communications (Cambridge, England), 2018, 54, 6192-6195
7121786 CIFC13 H8 Br2 O2P 1 21/n 115.484; 4.021; 19.824
90; 90.285; 90		1234.3Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121787 CIFC13 H8 Br2 O2P n a 217.859; 6.118; 24.872
90; 90; 90		1195.9Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121788 CIFC13 H8 Br2 O2P 21 21 213.8549; 11.732; 27.48
90; 90; 90		1242.8Saha, Subhankar; Desiraju, Gautam R.
Trimorphs of 4-bromophenyl 4-bromobenzoate. Elastic, brittle, plastic.
Chemical communications (Cambridge, England), 2018, 54, 6348-6351
7121789 CIFC28 H28 Br2 N2 O4P 21 21 218.3572; 15.2648; 20.6156
90; 90; 90		2629.95Jia, Hao; Guo, Zhenyan; Liu, Honglei; Mao, Biming; Shi, Xueyan; Guo, Hongchao
Tandem nucleophilic addition-cycloaddition of arynes with α-iminoesters: two concurrent pathways to imidazolidines.
Chemical communications (Cambridge, England), 2018, 54, 7050-7053
7121790 CIFC30 H27 N O4P 21 21 219.49079; 9.73586; 26.0784
90; 90; 90		2409.67Pawliczek, Martin; Shimazaki, Yuto; Kimura, Hidenori; Oberg, Kevin M.; Zakpur, Saman; Hashimoto, Takuya; Maruoka, Keiji
Phase-transfer-catalysed asymmetric synthesis of 2,2-disubstituted 1,4-benzoxazin-3-ones.
Chemical communications (Cambridge, England), 2018, 54, 7078-7080
7121791 CIFC36 H32 F3 N4 Nd O10P -110.1306; 11.4102; 17.3413
70.926; 88.066; 72.035		1797.08Sun, Si-Si; Zhang, Jian-Hua; Wang, Zheng; Yu, Yong-Qin; Zhu, Cheng-Yi; Pan, Mei; Su, Cheng-Yong
Anomalous thermally-activated NIR emission of ESIPT modulated Nd-complexes for optical fiber sensing devices.
Chemical communications (Cambridge, England), 2018, 54, 6304-6307
7121792 CIFC53 H41 B F20 Mg N2P -115.0751; 18.2135; 19.1996
79.2972; 86.7245; 72.6916		4945.36Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121793 CIFC65 H61 B F21 Mg N2 O PP -112.6579; 15.3343; 17.5503
92.793; 107.979; 99.369		3179.12Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121794 CIFC65 H53 B F20 Mg N2P -112.6783; 13.1414; 19.5127
100.801; 101.644; 110.656		2858.36Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121795 CIFC65 H53 B Ca F20 N2P 1 21/c 115.4894; 16.6388; 22.8557
90; 94.347; 90		5873.54Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121796 CIFC65 H71 B F20 Mg N2 O2 P2P -112.9094; 15.1447; 16.9144
94.761; 92.981; 96.921		3265.1Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121797 CIFC59 H51 B F20 Mg N2P 1 21/c 114.3528; 20.156; 19.2715
90; 100.557; 90		5480.8Pahl, Jürgen; Brand, Steffen; Elsen, Holger; Harder, Sjoerd
Highly Lewis acidic cationic alkaline earth metal complexes.
Chemical communications (Cambridge, England), 2018, 54, 8685-8688
7121798 CIFB5 F O8 PbP b c a10.885; 9.108; 13.576
90; 90; 90		1345.9Mutailipu, Miriding; Zhang, Min; Zhang, Bingbing; Yang, Zhihua; Pan, Shilie
The first lead fluorooxoborate PbB<sub>5</sub>O<sub>8</sub>F: achieving the coexistence of large birefringence and deep-ultraviolet cut-off edge.
Chemical communications (Cambridge, England), 2018, 54, 6308-6311
7121799 CIFBi7 Nd3I m m m4.2996; 15.2; 19.121
90; 90; 90		1249.6Ovchinnikov, Alexander; Makongo, Julien P. A.; Bobev, Svilen
Yet again, new compounds found in systems with known binary phase diagrams. Synthesis, crystal and electronic structure of Nd<sub>3</sub>Bi<sub>7</sub> and Sm<sub>3</sub>Bi<sub>7</sub>.
Chemical communications (Cambridge, England), 2018, 54, 7089-7092
7121800 CIFBi7 Sm3I m m m4.2762; 15.05; 19.034
90; 90; 90		1225Ovchinnikov, Alexander; Makongo, Julien P. A.; Bobev, Svilen
Yet again, new compounds found in systems with known binary phase diagrams. Synthesis, crystal and electronic structure of Nd<sub>3</sub>Bi<sub>7</sub> and Sm<sub>3</sub>Bi<sub>7</sub>.
Chemical communications (Cambridge, England), 2018, 54, 7089-7092
7121801 CIFC20 H15 N OP 1 21/n 113.107; 5.8099; 19.648
90; 102.575; 90		1460.3Jaiswal, Yogesh; Kumar, Yogesh; Pal, Jagannath; Subramanian, Ranga; Kumar, Amit
Rapid synthesis of polysubstituted phenanthridines from simple aliphatic/aromatic nitriles and iodo arenes via Pd(ii) catalyzed domino C-C/C-C/C-N bond formation.
Chemical communications (Cambridge, England), 2018, 54, 7207-7210
7121802 CIFC42 H72 Lu N3 Si3P 1 21/c 112.4709; 20.2287; 36.0755
90; 90.1168; 90		9100.8Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121803 CIFC57.5 H98 N3 O Si3 YP 1 21/n 118.7125; 31.04; 20.6586
90; 93.071; 90		11982Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121804 CIFC42 H72 N3 Sc Si3P 1 21/c 112.3546; 20.0869; 35.9838
90; 90.113; 90		8929.9Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121805 CIFC42 H72 N3 Si3 YP 1 21/c 112.5095; 20.2927; 36.0731
90; 90.412; 90		9157Boteju, Kasuni C.; Wan, Suchen; Venkatesh, Amrit; Ellern, Arkady; Rossini, Aaron J.; Sadow, Aaron D.
Rare earth arylsilazido compounds with inequivalent secondary interactions.
Chemical communications (Cambridge, England), 2018, 54, 7318-7321
7121808 CIFC24 H35 B N6 O2 Si WP 1 21/c 19.3555; 14.6772; 20.6011
90; 89.668; 90		2828.74Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121809 CIFC25 H37 B N6 O2 Si WP 1 21/c 112.636; 14.8272; 16.3046
90; 109.839; 90		2873.47Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121810 CIFC53 H80 B2 N12 O4 Si2 W2P -111.0937; 13.1532; 22.7516
91.059; 98.161; 108.441		3110.38Frogley, Benjamin J.; Hill, Anthony F.
Bis(alkylidynyl)arsines.
Chemical communications (Cambridge, England), 2018, 54, 7649-7652
7121811 CIFC19 H18 Cl N OC 1 2/c 120.1159; 8.9951; 17.9253
90; 93.382; 90		3237.8Gupta, Sonu; Chandna, Nisha; Dubey, Pooja; Singh, Ajai K.; Jain, Nidhi
GO-Cu<sub>7</sub>S<sub>4</sub> catalyzed ortho-aminomethylation of phenol derivatives with N,N-dimethylbenzylamines: site-selective oxidative CDC.
Chemical communications (Cambridge, England), 2018, 54, 7511-7514
7121812 CIFC12 H14 N2 OP 21 21 215.7386; 9.5416; 18.3137
90; 90; 90		1002.77Wu, Kui; Du, Yuliu; Wei, Zheng; Wang, Ting
Synthesis of functionalized pyrroloindolines via a visible-light-induced radical cascade reaction: rapid synthesis of (±)-flustraminol B.
Chemical communications (Cambridge, England), 2018, 54, 7443-7446
7121813 CIFC13 H16 N2 O2C 1 2/c 128.7011; 9.388; 8.9139
90; 99.23; 90		2370.7Wu, Kui; Du, Yuliu; Wei, Zheng; Wang, Ting
Synthesis of functionalized pyrroloindolines via a visible-light-induced radical cascade reaction: rapid synthesis of (±)-flustraminol B.
Chemical communications (Cambridge, England), 2018, 54, 7443-7446
7121814 CIFC26 H37 N O PP -110.0822; 10.8747; 12.0033
106.883; 90.592; 103.9		1217.9Mai, Juri; Arkhypchuk, Anna I.; Gupta, Arvind Kumar; Ott, Sascha
Reductive coupling of two aldehydes to unsymmetrical E-alkenes via phosphaalkene and phosphinate intermediates.
Chemical communications (Cambridge, England), 2018, 54, 7163-7166
7121815 CIFC57 H85 Cl3 N2 O6 P2P -110.7916; 17.0045; 17.0443
90.205; 96.705; 106.832		2971Mai, Juri; Arkhypchuk, Anna I.; Gupta, Arvind Kumar; Ott, Sascha
Reductive coupling of two aldehydes to unsymmetrical E-alkenes via phosphaalkene and phosphinate intermediates.
Chemical communications (Cambridge, England), 2018, 54, 7163-7166
7121816 CIFC209 H298 N36 O33 P2P -119.83; 22.082; 27.967
86.839; 77.529; 75.246		11563Zuo, Wei; Huang, Zhe; Zhao, Yanxia; Xu, Wenhua; Liu, Zhihua; Yang, Xiao-Juan; Jia, Chuandong; Wu, Biao
Chirality sensing of choline derivatives by a triple anion helicate cage through induced circular dichroism.
Chemical communications (Cambridge, England), 2018, 54, 7378-7381
7121817 CIFC22 H29 I N2 O3P -19.0399; 10.7529; 12.1907
84.915; 70.321; 80.746		1100.51Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121818 CIFC44 H58 Cl2 N4 O6P -17.9255; 9.259; 15.1784
96.993; 98.728; 98.758		1076.06Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121819 CIFC46 H55 F12 N7 O4 P2P 1 21/c 112.698; 17.0155; 23.0412
90; 96.201; 90		4949.2Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121820 CIFC44 H58 Br2 N4 O6P 1 21/c 18.303; 28.106; 9.5912
90; 104.697; 90		2165Tam, Teck Lip Dexter; Ng, Chee Koon; Lu, Xuefeng; Lim, Zheng Long; Wu, Jishan
Anion-π interactions of highly π-acidic dipyridinium-naphthalene diimide salts.
Chemical communications (Cambridge, England), 2018, 54, 7374-7377
7121821 CIFCe2 Cl12 Ni4F m -3 m10.1404; 10.1404; 10.1404
90; 90; 90		1042.7Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121822 CIFCl12 Eu2 Ni4F m -3 m10.1666; 10.1666; 10.1666
90; 90; 90		1050.8Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121823 CIFCl12 Gd2 Ni4F m -3 m10.1164; 10.1164; 10.1164
90; 90; 90		1035.33Baldo, Bianca; Rubio, Francisco; Flores, Erwin; Vega, Andres; Audebrand, Nathalie; Venegas-Yazigi, Diego; Paredes-García, Verónica
Ni<sub>2</sub>[LnCl<sub>6</sub>] (Ln = Eu<sup>II</sup>, Ce<sup>II</sup>, Gd<sup>II</sup>): the first Ln<sup>II</sup> compounds stabilized in a pure inorganic lattice.
Chemical communications (Cambridge, England), 2018, 54, 7531-7534
7121824 CIFC57 H71 B N4P -110.344; 15.31; 15.375
96.097; 93.5; 101.648		2363Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121825 CIFC34 H56 B N5 SiP 1 21/n 119.1168; 17.0388; 21.9556
90; 105.534; 90		6890.3Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121826 CIFC50 H59 B N4P -113.134; 16.944; 19.889
79.28; 81.864; 73.209		4145Winner, Lena; Hermann, Alexander; Bélanger-Chabot, Guillaume; González-Belman, Oscar F; Jiménez-Halla, J Oscar C; Kelch, Hauke; Braunschweig, Holger
Cleavage of BN triple bonds by main group reagents.
Chemical communications (Cambridge, England), 2018, 54, 8210-8213
7121828 CIFC17 H13 F2 N O2P b c a8.3324; 18.0049; 18.9382
90; 90; 90		2841.2Ma, Xingxing; Mai, Shaoyu; Zhou, Yao; Cheng, Gui-Juan; Song, Qiuling
Dual role of ethyl bromodifluoroacetate in the formation of fluorine-containing heteroaromatic compounds.
Chemical communications (Cambridge, England), 2018, 54, 8960-8963
7121829 CIFC34 H40 N2 O14 S12 ZnP 1 21/c 114.0234; 10.7448; 15.7641
90; 94.765; 90		2367.1Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121830 CIFC34 H40 Mn N2 O14 S12P 1 21/c 113.904; 10.668; 15.757
90; 95.34; 90		2327.1Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121831 CIFC34 H40 N2 O14 S12 ZnP 1 21/c 113.956; 10.755; 15.612
90; 94.237; 90		2336.9Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121832 CIFC34 H40 Mn N2 O14 S12P 1 21/c 113.957; 10.7952; 15.701
90; 94.815; 90		2357.3Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121833 CIFC34 H42 N2 O14 S12 ZnP 1 21/c 114.2765; 10.2073; 16.037
90; 92.05; 90		2335.5Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121834 CIFC34 H42 Mn N2 O14 S12P 1 21/c 114.0309; 10.3024; 16.0378
90; 93.634; 90		2313.6Zhang, Ping; Huo, Peng; Zhang, Xuan; Zhu, Qin-Yu; Dai, Jie
C-C to C[double bond, length as m-dash]C conversion within a supramolecular framework of tetrathiafulvalene: a confinement effect and an oxygen related dehydrogenation.
Chemical communications (Cambridge, England), 2018, 54, 7334-7337
7121835 CIFC7 H11 N O4P 1 21/n 19.7222; 7.91107; 11.6743
90; 102.086; 90		878Riemer, Martin; Uzunova, Veselina V.; Riemer, Nastja; Clarkson, Guy J.; Pereira, Nicole; Napier, Richard; Shipman, Michael
Phyllostictine A: total synthesis, structural verification and determination of substructure responsible for plant growth inhibition.
Chemical communications (Cambridge, England), 2018, 54, 7211-7214
7121836 CIFC14 H25 N O5P 1 21/c 115.5057; 9.2475; 11.6104
90; 108.886; 90		1575.17Hayashi, Hirohito; Kaga, Atsushi; Wang, Bin; Gagosz, Fabien; Chiba, Shunsuke
Use of a benzyl ether as a traceless hydrogen donor in the anti-Markovnikov hydrofunctionalization of alkenes with xanthates.
Chemical communications (Cambridge, England), 2018, 54, 7535-7538
7121837 CIFC H4 Cl3 K N2 O ZnP 1 21/m 16.8599; 7.353; 8.4999
90; 99.069; 90		423.38Casali, Lucia; Mazzei, Luca; Shemchuk, Oleksii; Honer, Kenneth; Grepioni, Fabrizia; Ciurli, Stefano; Braga, Dario; Baltrusaitis, Jonas
Smart urea ionic co-crystals with enhanced urease inhibition activity for improved nitrogen cycle management.
Chemical communications (Cambridge, England), 2018, 54, 7637-7640
7121838 CIFC H4 Cl3 K N2 O ZnP 1 21/n 17.422; 13.553; 8.4219
90; 92.089; 90		846.6Casali, Lucia; Mazzei, Luca; Shemchuk, Oleksii; Honer, Kenneth; Grepioni, Fabrizia; Ciurli, Stefano; Braga, Dario; Baltrusaitis, Jonas
Smart urea ionic co-crystals with enhanced urease inhibition activity for improved nitrogen cycle management.
Chemical communications (Cambridge, England), 2018, 54, 7637-7640
7121839 CIFC14 H16 N2 O2 SP 1 21 19.955; 5.5629; 12.732
90; 92.902; 90		704.2Wang, Miao; Tang, Bo-Cheng; Wang, Jun-Gang; Xiang, Jia-Chen; Guan, Ao-Yu; Huang, Ping-Ping; Guo, Wu-Yinzheng; Wu, Yan-Dong; Wu, An-Xin
The triple role of rongalite in aminosulfonylation of aryldiazonium tetrafluoroborates: synthesis of N-aminosulfonamides via a radical coupling reaction.
Chemical communications (Cambridge, England), 2018, 54, 7641-7644
7121840 CIFC17 H18 O4P 1 21 17.69761; 12.2794; 8.18769
90; 110.677; 90		724.07Shu, Tao; Li, Sun; Chen, Xiang-Yu; Liu, Qiang; von Essen, Carolina; Rissanen, Kari; Enders, Dieter
Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition.
Chemical communications (Cambridge, England), 2018, 54, 7661-7664
7121841 CIFC25 H34 N4 SP 1 21/n 115.443; 11.2028; 15.4669
90; 117.896; 90		2364.9Ruamps, Mirko; Bastin, Stéphanie; Rechignat, Lionel; Sournia-Saquet, Alix; Valyaev, Dmitry A.; Mouesca, Jean-Marie; Lugan, Noël; Maurel, Vincent; César, Vincent
Unveiling the redox-active character of imidazolin-2-thiones derived from amino-substituted N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2018, 54, 7653-7656
7121842 CIFC27 H37 F12 N5 S Sb2P -111.9044; 12.9628; 13.2255
60.88; 78.818; 80.295		1742.51Ruamps, Mirko; Bastin, Stéphanie; Rechignat, Lionel; Sournia-Saquet, Alix; Valyaev, Dmitry A.; Mouesca, Jean-Marie; Lugan, Noël; Maurel, Vincent; César, Vincent
Unveiling the redox-active character of imidazolin-2-thiones derived from amino-substituted N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2018, 54, 7653-7656
7121843 CIFC17 H28 O6P 21 21 217.6651; 12.4842; 18.5353
90; 90; 90		1773.69Feng, Jing; Yu, Tianzi; Zhang, Zhijiang; Li, Jinpeng; Fu, Shaomin; Chen, Juan; Liu, Bo
Asymmetric synthesis of the fully functionalized six-membered ring of trigoxyphin A.
Chemical communications (Cambridge, England), 2018, 54, 7665-7668
7121844 CIFC17 H26 O7P 21 21 218.9598; 11.7903; 17.2249
90; 90; 90		1819.62Feng, Jing; Yu, Tianzi; Zhang, Zhijiang; Li, Jinpeng; Fu, Shaomin; Chen, Juan; Liu, Bo
Asymmetric synthesis of the fully functionalized six-membered ring of trigoxyphin A.
Chemical communications (Cambridge, England), 2018, 54, 7665-7668
7121845 CIFC19 H18 N2P b c a10.619; 9.676; 28.661
90; 90; 90		2944.9Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121846 CIFC20 H20 N2P 1 21/n 19.4242; 7.9644; 19.9745
90; 99.582; 90		1478.33Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121847 CIFC41 H43 N4P 1 21/c 120.821; 9.5022; 17.881
90; 110.124; 90		3321.7Liu, Siyuan; Qu, Jingping; Wang, Baomin
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades.
Chemical communications (Cambridge, England), 2018, 54, 7928-7931
7121848 CIFC33 H30 N2 O2 SP 1 21/n 17.7368; 16.8658; 20.2866
90; 96.461; 90		2630.3Pradhan, Sajan; Shahi, Chandan Kumar; Bhattacharyya, Aditya; Ghorai, Manas K.
Stereoselective synthesis of 3-spiropiperidino indolenines via S<sub>N</sub>2-type ring opening of activated aziridines with 1H-indoles/Pd-catalyzed spirocyclization with propargyl carbonates.
Chemical communications (Cambridge, England), 2018, 54, 8583-8586
7121849 CIFC66 H64 O12P -19.3274; 12.0859; 12.4207
110.921; 90.774; 98.445		1290.4Chai, Hongxin; Yang, Liu-Pan; Ke, Hua; Pang, Xin-Yu; Jiang, Wei
Allosteric cooperativity in ternary complexes with low symmetry.
Chemical communications (Cambridge, England), 2018, 54, 7677-7680
7121850 CIFC67 H66 Cl2 O12P -112.3158; 12.769; 19.5858
85.884; 73.714; 80.961		2918.52Chai, Hongxin; Yang, Liu-Pan; Ke, Hua; Pang, Xin-Yu; Jiang, Wei
Allosteric cooperativity in ternary complexes with low symmetry.
Chemical communications (Cambridge, England), 2018, 54, 7677-7680
7121851 CIFC22 H23 F OP 1 21/c 112.6134; 8.4407; 17.1212
90; 94.76; 90		1816.54Xu, Ming-Hui; Dai, Kun-Long; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
A catalytic allylic cation-induced intermolecular allylation-semipinacol rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 7685-7688
7121852 CIFC28 H28 OP n a 2118.308; 19.0516; 6.2276
90; 90; 90		2172.17Xu, Ming-Hui; Dai, Kun-Long; Tu, Yong-Qiang; Zhang, Xiao-Ming; Zhang, Fu-Min; Wang, Shao-Hua
A catalytic allylic cation-induced intermolecular allylation-semipinacol rearrangement.
Chemical communications (Cambridge, England), 2018, 54, 7685-7688
7121853 CIFC17 H21 Br Cl N2 O RhP b c a15.4304; 14.9823; 16.4747
90; 90; 90		3808.7He, Shuang; Tan, Guangying; Luo, Anping; You, Jingsong
Rhodium-catalyzed oxidative C-H/C-H cross-coupling of aniline with heteroarene: N-nitroso group enabled mild conditions.
Chemical communications (Cambridge, England), 2018, 54, 7794-7797
7121854 CIFC65 H64 B Cl F20 Mg N2 O Si2P -113.3518; 14.4685; 17.3377
98.233; 97.872; 90.686		3281.8Pahl, Jürgen; Elsen, Holger; Friedrich, Alexander; Harder, Sjoerd
Unsupported metal silyl ether coordination.
Chemical communications (Cambridge, England), 2018, 54, 7846-7849
7121855 CIFC44 H42 N2 O4 S2P -17.2994; 9.0319; 14.3088
84.935; 77.163; 84.614		913.49Hu, Yingyuan; Wang, Zhenfeng; Jiang, Xiaofang; Cai, Xinyi; Su, Shi-Jian; Huang, Fei; Cao, Yong
One-step synthesis of cyclic compounds towards easy room-temperature phosphorescence and deep blue thermally activated delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 7850-7853
7121856 CIFC38 H30 N2 O6 S2P 1 21/c 113.5501; 4.9755; 23.1851
90; 100.243; 90		1538.19Hu, Yingyuan; Wang, Zhenfeng; Jiang, Xiaofang; Cai, Xinyi; Su, Shi-Jian; Huang, Fei; Cao, Yong
One-step synthesis of cyclic compounds towards easy room-temperature phosphorescence and deep blue thermally activated delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 7850-7853
7121857 CIFC30 H28 F12 N8 Ni P2P 1 21/c 110.7258; 18.871; 16.3402
90; 93.244; 90		3302.1Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121858 CIFC30 H28 F12 N8 Ni P2P 21 21 2111.199; 15.1982; 19.638
90; 90; 90		3342.5Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121859 CIFC28 H24 F6 N7 Ni PP 1 21/n 18.3433; 28.32; 11.5936
90; 90.533; 90		2739.2Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121860 CIFC32 H31 F12 N9 P2 PdP 1 21/c 114.6723; 13.3927; 19.2473
90; 108.953; 90		3577.1Yang, Chu-Fan; Lu, Taotao; Chen, Xue-Tai; Xue, Zi-Ling
Unusual rearrangement of an N-heterocyclic carbene via a ring-opening and ring-closing process.
Chemical communications (Cambridge, England), 2018, 54, 7830-7833
7121861 CIFC42 H40 N4R -3 :H26.1757; 26.1757; 31.6025
90; 90; 120		18752Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121862 CIFC60 H77 F3 N6 O0.29P -111.5785; 13.3678; 19.1989
80.99; 73.141; 82.786		2798.7Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121863 CIFC46 H46 N6P 1 21/c 111.27; 14.844; 12.708
90; 114.23; 90		1938.7Dutta, Ranjan; Firmansyah, Dikhi; Kim, Jihoon; Jo, Hongil; Ok, Kang Min; Lee, Chang-Hee
Unexpected halide anion binding modes in meso-bis-ethynyl picket-calix[4]pyrroles: effects of meso-π (ethynyl) extension.
Chemical communications (Cambridge, England), 2018, 54, 7936-7939
7121864 CIFC18 H24 O7P 1 21/c 17.31; 24.5621; 10.1151
90; 91.383; 90		1815.6Burnie, Andrew J.; Evans, P. Andrew
Rhodium-catalyzed [(3+2)+1] carbocyclizations of alkynylidenecyclopropanes with carbon monoxide: construction of polysubstituted bicyclohexa-2,5-dienones.
Chemical communications (Cambridge, England), 2018, 54, 7621-7624
7121865 CIFC57.18 H44.44 O40 S4 Zr6I 4/m m m23.3559; 23.3559; 26.7429
90; 90; 90		14588.2Du, Pei-Yao; Lustig, William P.; Teat, Simon J.; Gu, Wen; Liu, Xin; Li, Jing
A robust two-dimensional zirconium-based luminescent coordination polymer built on a V-shaped dicarboxylate ligand for vapor phase sensing of volatile organic compounds.
Chemical communications (Cambridge, England), 2018, 54, 8088-8091
7121866 CIFC18 H30 Cl F2 N O10P c a 2114.558; 11.247; 14.392
90; 90; 90		2356.5Wei, Yan-Li; Jing, Jing; Shi, Chao; Ye, Heng-Yun; Wang, Zhong-Xia; Zhang, Yi
Unusual high-temperature reversible phase transition containing dielectric and nonlinear optical switches in host-guest supramolecular crown ether clathrates.
Chemical communications (Cambridge, England), 2018, 54, 8076-8079
7121867 CIFC18 H30 Cl F2 N O10P c a 2114.5486; 11.2914; 14.5674
90; 90; 90		2393Wei, Yan-Li; Jing, Jing; Shi, Chao; Ye, Heng-Yun; Wang, Zhong-Xia; Zhang, Yi
Unusual high-temperature reversible phase transition containing dielectric and nonlinear optical switches in host-guest supramolecular crown ether clathrates.
Chemical communications (Cambridge, England), 2018, 54, 8076-8079
7121868 CIFC5 H9 I2 N2 PC 1 2/m 113.4578; 8.6203; 9.8671
90; 116.365; 90		1025.62Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121869 CIFC18 H32 I N4 PI 1 2/a 19.4547; 19.5345; 11.8695
90; 94.891; 90		2184.2Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121870 CIFC9 H17 I2 N2 PP -17.7774; 8.4078; 11.6208
84.753; 79.435; 78.409		730.6Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121871 CIFC27 H37 I4 N2 PC 1 c 112.5136; 16.67; 16.872
90; 108.146; 90		3344.5Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121872 CIFC21 H25 I2 N2 PP 21 21 219.253; 15.3097; 16.0029
90; 90; 90		2267Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121873 CIFC28 H39 Cl2 I2 N2 PP 1 21/n 110.7558; 18.7258; 16.3345
90; 102.309; 90		3214.3Cicač-Hudi, M; Schlindwein, S. H.; Feil, C. M.; Nieger, M.; Gudat, D.
Isolable N-heterocyclic carbene adducts of the elusive diiodophosphine.
Chemical communications (Cambridge, England), 2018, 54, 7645-7648
7121874 CIFC23 H30 O4P 1 21/n 117.18; 6.536; 17.28
90; 91.34; 90		1940Yao, Sheng; Zhang, Kai; Zhou, Quan-Quan; Zhao, Yu; Shi, De-Qing; Xiao, Wen-Jing
Photoredox-promoted alkyl radical addition/semipinacol rearrangement sequences of alkenylcyclobutanols: rapid access to cyclic ketones.
Chemical communications (Cambridge, England), 2018, 54, 8096-8099
7121875 CIFC14 H16 Cl2 N2 O6P -14.9143; 7.458; 11.698
73.27; 89.528; 69.737		383.2Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121876 CIFC14 H16 Cl2 N2 O6P -14.987; 7.592; 11.718
72.926; 89.449; 71.157		399.6Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121877 CIFC14 H16 Cl2 N2 O6P -14.6904; 8.921; 9.833
103.357; 96.447; 93.984		395.8Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121878 CIFC14 H16 Cl2 N2 O6P -18.1575; 10.3671; 11.0921
74.29; 75.655; 67.442		822.93Donoshita, Masaki; Hayashi, Mikihiro; Ikeda, Ryuichi; Yoshida, Yukihiro; Morikawa, Shota; Sugimoto, Kunihisa; Kitagawa, Hiroshi
Drastic rearrangement of self-assembled hydrogen-bonded tapes in a molecular crystal.
Chemical communications (Cambridge, England), 2018, 54, 8571-8574
7121879 CIFC68 H98 Si3P 1 21/n 119.538; 14.015; 24.33
90; 108.596; 90		6314Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121880 CIFC135 H202 Si6C 1 2/c 140.86; 14.207; 23.479
90; 96.47; 90		13543Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121881 CIFC74 H102 Si3P -118.411; 20.736; 22.03
110.122; 100.632; 100.34		7488Zhao, Hui; Klemmer, Lukas; Cowley, Michael J.; Majumdar, Moumita; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Phenylene-bridged cross-conjugated 1,2,3-trisilacyclopentadienes.
Chemical communications (Cambridge, England), 2018, 54, 8399-8402
7121882 CIFC36 H24P 1 21/c 111.1772; 10.312; 11.2725
90; 106.329; 90		1246.85Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121883 CIFC64 H80 Na O10P 1 21/c 110.1288; 17.237; 16.0129
90; 102.514; 90		2729.28Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121884 CIFC76 H104 K2 O16P 1 21/n 110.1496; 23.2584; 15.4171
90; 98.784; 90		3596.73Spisak, Sarah N.; Wei, Zheng; Darzi, Evan; Jasti, Ramesh; Petrukhina, Marina A.
Highly strained [6]cycloparaphenylene: crystallization of an unsolvated polymorph and the first mono- and dianions.
Chemical communications (Cambridge, England), 2018, 54, 7818-7821
7121885 CIFC8 H14 Br3 N3 OP 1 21/c 16.4062; 20.4294; 9.5955
90; 92.369; 90		1254.74Weinberger, Craig; Hines, Rachel; Zeller, Matthias; Rosokha, Sergiy V.
Continuum of covalent to intermolecular bonding in the halogen-bonded complexes of 1,4-diazabicyclo[2.2.2]octane with bromine-containing electrophiles.
Chemical communications (Cambridge, England), 2018, 54, 8060-8063

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