Crystallography Open Database

Result: there are 4887 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching volume of publication is 18

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 5 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
7157401 CIFC51 H44 Cl3 N5 OP -111.977; 12.739; 17.798
98.842; 98.679; 107.964		2495Kato, Shin-Ichiro; Kijima, Tomokazu; Shiota, Yoshihito; Abe, Tsukasa; Kuwako, Satoshi; Miyauchi, Hidenori; Yoshikawa, Naoki; Yamamoto, Koji; Yoshizawa, Kazunari; Yoshihara, Toshitada; Tobita, Seiji; Nakamura, Yosuke
Chemical transformations of push-pull fluorenones: push-pull dibenzodicyanofulvenes as well as fluorenone- and dibenzodicyanofulvene-tetracyanobutadiene conjugates.
Organic & biomolecular chemistry, 2020, 18, 4198-4209
7157402 CIFC52 H41 N7P 1 21/n 117.349; 13.933; 19.572
90; 100.366; 90		4653.8Kato, Shin-Ichiro; Kijima, Tomokazu; Shiota, Yoshihito; Abe, Tsukasa; Kuwako, Satoshi; Miyauchi, Hidenori; Yoshikawa, Naoki; Yamamoto, Koji; Yoshizawa, Kazunari; Yoshihara, Toshitada; Tobita, Seiji; Nakamura, Yosuke
Chemical transformations of push-pull fluorenones: push-pull dibenzodicyanofulvenes as well as fluorenone- and dibenzodicyanofulvene-tetracyanobutadiene conjugates.
Organic & biomolecular chemistry, 2020, 18, 4198-4209
7157403 CIFC53 H43 N7P -112.037; 13.922; 16.102
91.4728; 111.807; 109.604		2324.9Kato, Shin-Ichiro; Kijima, Tomokazu; Shiota, Yoshihito; Abe, Tsukasa; Kuwako, Satoshi; Miyauchi, Hidenori; Yoshikawa, Naoki; Yamamoto, Koji; Yoshizawa, Kazunari; Yoshihara, Toshitada; Tobita, Seiji; Nakamura, Yosuke
Chemical transformations of push-pull fluorenones: push-pull dibenzodicyanofulvenes as well as fluorenone- and dibenzodicyanofulvene-tetracyanobutadiene conjugates.
Organic & biomolecular chemistry, 2020, 18, 4198-4209
7157404 CIFC47 H43 N3P 1 21/c 115.001; 16.5592; 30.27
90; 100.711; 90		7388.2Kato, Shin-Ichiro; Kijima, Tomokazu; Shiota, Yoshihito; Abe, Tsukasa; Kuwako, Satoshi; Miyauchi, Hidenori; Yoshikawa, Naoki; Yamamoto, Koji; Yoshizawa, Kazunari; Yoshihara, Toshitada; Tobita, Seiji; Nakamura, Yosuke
Chemical transformations of push-pull fluorenones: push-pull dibenzodicyanofulvenes as well as fluorenone- and dibenzodicyanofulvene-tetracyanobutadiene conjugates.
Organic & biomolecular chemistry, 2020, 18, 4198-4209
7157405 CIFC46.5 H43 N3 O0.5P -113.3124; 17.3674; 17.7864
78.525; 77.087; 70.127		3735.5Kato, Shin-Ichiro; Kijima, Tomokazu; Shiota, Yoshihito; Abe, Tsukasa; Kuwako, Satoshi; Miyauchi, Hidenori; Yoshikawa, Naoki; Yamamoto, Koji; Yoshizawa, Kazunari; Yoshihara, Toshitada; Tobita, Seiji; Nakamura, Yosuke
Chemical transformations of push-pull fluorenones: push-pull dibenzodicyanofulvenes as well as fluorenone- and dibenzodicyanofulvene-tetracyanobutadiene conjugates.
Organic & biomolecular chemistry, 2020, 18, 4198-4209
7157406 CIFC29 H32 Cl N O5P 1 21 19.6244; 9.8943; 14.3864
90; 94.36; 90		1366Zhou, Jing; Bai, Li-Juan; Liang, Guo-Juan; Xu, Qi-Gui; Zhou, Li-Ping; Zhou, Hui
Organocatalytic asymmetric cascade 1,6-addition/hemiketalization/retro-Henry reaction of ortho-hydroxyphenyl-substituted p-QMs with α-nitroketones.
Organic & biomolecular chemistry, 2020, 18, 2641-2645
7157407 CIFC10 H13 Br Cl O4 PP 1 21/n 18.7086; 9.0359; 17.1804
90; 102.801; 90		1318.3Wang, Zexu; Zeng, Yiping; Wu, Xiaofan; Li, Zihan; Tao, Yuan; Yu, Xiaomin; Huang, Zedu; Chen, Fener
Access to chiral α-substituted-β-hydroxy arylphosphonates enabled by biocatalytic dynamic reductive kinetic resolution.
Organic & biomolecular chemistry, 2020, 18, 2672-2677
7157408 CIFC10 H13 Br Cl O4 PP 21 21 218.7884; 9.1062; 34.664
90; 90; 90		2774.12Wang, Zexu; Zeng, Yiping; Wu, Xiaofan; Li, Zihan; Tao, Yuan; Yu, Xiaomin; Huang, Zedu; Chen, Fener
Access to chiral α-substituted-β-hydroxy arylphosphonates enabled by biocatalytic dynamic reductive kinetic resolution.
Organic & biomolecular chemistry, 2020, 18, 2672-2677
7157409 CIFC18 H21 N O6P 21 21 215.7158; 16.615; 19.036
90; 90; 90		1807.8Popik, Oskar; Grzeszczyk, Barbara; Staszewska-Krajewska, Olga; Furman, Bartłomiej; Chmielewski, Marek
Synthesis of β-lactams via diastereoselective, intramolecular Kinugasa reactions.
Organic & biomolecular chemistry, 2020, 18, 2852-2860
7157410 CIFC105 H74 Cl2 N8 O2P 1 21 110.19377; 39.0375; 11.437
90; 116.788; 90		4062.81Kubo, Masahiro; Takase, Ko; Noguchi, Keiichi; Nakano, Koji
Solvent-sensitive circularly polarized luminescent compounds bearing a 9,9'-spirobi[fluorene] skeleton.
Organic & biomolecular chemistry, 2020, 18, 2866-2876
7157411 CIFC14 H11 N3 OP 1 21/c 15.4509; 19.981; 10.8572
90; 103.309; 90		1150.7Shamanth, Sadashivamurthy; Chaithra, Nagaraju; Gurukiran, Mahesha; Mamatha, Mahesha; Lokanath, N. K.; Rangappa, Kanchugarakoppal S.; Mantelingu, Kempegowda
I<sub>2</sub>-Catalyzed transformation of o-aminobenzamide to o-ureidobenzonitrile using isothiocyanates.
Organic & biomolecular chemistry, 2020, 18, 2678-2684
7157412 CIFC16 H20 B F O2P 21 21 218.532; 11.8108; 14.1961
90; 90; 90		1430.54Martínez-Aguirre, Mayte A; Flores-Alamo, Marcos; Medrano, Felipe; Yatsimirsky, Anatoly K.
Examination of pinanediol-boronic acid ester formation in aqueous media: relevance to the relative stability of trigonal and tetrahedral boronate esters.
Organic & biomolecular chemistry, 2020, 18, 2716-2726
7157413 CIFC18 H25 B O3P 21 21 216.2351; 12.5482; 20.861
90; 90; 90		1632.1Martínez-Aguirre, Mayte A; Flores-Alamo, Marcos; Medrano, Felipe; Yatsimirsky, Anatoly K.
Examination of pinanediol-boronic acid ester formation in aqueous media: relevance to the relative stability of trigonal and tetrahedral boronate esters.
Organic & biomolecular chemistry, 2020, 18, 2716-2726
7157414 CIFC106.12 H104.87 Cl12 N24 O8.53 Zn6C 1 2 134.1049; 14.4311; 31.2664
90; 102.554; 90		15020.5Morishita, Yohei; Sonohara, Terutaka; Taniguchi, Tohru; Adachi, Kiyohiro; Fujita, Makoto; Asai, Teigo
Synthetic-biology-based discovery of a fungal macrolide from Macrophomina phaseolina.
Organic & biomolecular chemistry, 2020, 18, 2813-2816
7157415 CIFC31 H34 Cl N O3P 21 21 2110.3478; 14.7058; 18.6178
90; 90; 90		2833.1Qi, Suo-Suo; Jiang, Zhen-Hui; Chu, Ming-Ming; Wang, Yi-Feng; Chen, Xue-Yang; Ju, Wan-Zhen; Xu, Dan-Qian
Regioselective catalytic asymmetric N-alkylation of isoxazol-5-ones with para-quinone methides.
Organic & biomolecular chemistry, 2020, 18, 2398-2404
7157416 CIFC21 H23 N O2P 1 21/n 113.583; 8.561; 15.116
90; 97.03; 90		1744.5Ning, Yi; He, Xinwei; Zuo, Youpeng; Wang, Jian; Tang, Qiang; Xie, Mengqing; Li, Ruxue; Shang, Yongjia
Rh-Catalyzed C-H activation/intramolecular condensation for the construction of benzo[f]pyrazolo[1,5-a][1,3]diazepines.
Organic & biomolecular chemistry, 2020, 18, 2893-2901
7157417 CIFC18 H19 N3 OP 1 21/c 17.2409; 19.433; 10.923
90; 95.667; 90		1529.5Ning, Yi; He, Xinwei; Zuo, Youpeng; Wang, Jian; Tang, Qiang; Xie, Mengqing; Li, Ruxue; Shang, Yongjia
Rh-Catalyzed C-H activation/intramolecular condensation for the construction of benzo[f]pyrazolo[1,5-a][1,3]diazepines.
Organic & biomolecular chemistry, 2020, 18, 2893-2901
7157418 CIFC15 H12 O2 SP 21 21 217.5756; 8.7063; 19.34
90; 90; 90		1275.6Gharui, Chandan; Prakash, Satya; Chopra, Deepak; Pan, Subhas Chandra
Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones.
Organic & biomolecular chemistry, 2020, 18, 2828-2833
7157419 CIFC17 H16 O4 SP 21 21 27.969; 34.663; 5.361
90; 90; 90		1480.9Gharui, Chandan; Prakash, Satya; Chopra, Deepak; Pan, Subhas Chandra
Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones.
Organic & biomolecular chemistry, 2020, 18, 2828-2833
7157420 CIFC37 H40 O2 P2P 21 21 2112.9764; 14.3781; 17.5765
90; 90; 90		3279.4Qiu, Mao-Ran; Zheng, Hong-Xing; Ye, Jing-Jing; Yan, Bing-Xia; Zhao, Chang-Qiu; Li, Qiang
Stereoselective preparation of P,axial-stereogenic allenyl bisphosphine oxides via chirality-transfer.
Organic & biomolecular chemistry, 2020, 18, 3017-3021
7157421 CIFC38 H42 O2 P2P 21 21 2113.2801; 14.3298; 17.9616
90; 90; 90		3418.1Qiu, Mao-Ran; Zheng, Hong-Xing; Ye, Jing-Jing; Yan, Bing-Xia; Zhao, Chang-Qiu; Li, Qiang
Stereoselective preparation of P,axial-stereogenic allenyl bisphosphine oxides via chirality-transfer.
Organic & biomolecular chemistry, 2020, 18, 3017-3021
7157422 CIFC26 H33 O3 PP 21 21 218.8154; 11.3911; 24.121
90; 90; 90		2422.2Qiu, Mao-Ran; Zheng, Hong-Xing; Ye, Jing-Jing; Yan, Bing-Xia; Zhao, Chang-Qiu; Li, Qiang
Stereoselective preparation of P,axial-stereogenic allenyl bisphosphine oxides via chirality-transfer.
Organic & biomolecular chemistry, 2020, 18, 3017-3021
7157423 CIFC28 H28 N2 O2 SP 1 21/c 114.276; 14.392; 11.161
90; 94.34; 90		2287Zakharov, A. V.; Yadykov, A. V.; Lvov, A. G.; Mitina, E. A.; Shirinian, V. Z.
Photochemical rearrangement of diarylethenes: synthesis of functionalized phenanthrenes.
Organic & biomolecular chemistry, 2020, 18, 3098-3103
7157424 CIFC18 H14 N2 O3P 1 21/c 19.531; 7.0315; 21.6758
90; 93.267; 90		1450.29Ritu, ?; Sharma, Charu; Kumar, Sharvan; Jain, Nidhi
Singlet oxygen mediated dual C-C and C-N bond cleavage in visible light.
Organic & biomolecular chemistry, 2020, 18, 2921-2928
7157425 CIFC55 H34 F12 N4C 1 2/c 131.975; 7.5139; 20.464
90; 115.609; 90		4433.6Thomas, Kolle E.; Conradie, Jeanet; Beavers, Christine M.; Ghosh, Abhik
Free-base porphyrins with localized NH protons. Can substituents alone stabilize the elusive cis tautomer?
Organic & biomolecular chemistry, 2020, 18, 2861-2865
7157426 CIFC25 H29 N O4P 19.0309; 13.028; 19.9637
99.064; 98.729; 91.614		2289.36Chen, Jian-Ping; Xu, Ming-Hua
Chiral diene-promoted room temperature conjugate arylation: highly enantioselective synthesis of substituted chiral phenylalanine derivatives and α,α-di(arylmethyl)acetates.
Organic & biomolecular chemistry, 2020, 18, 4569-4574
7157427 CIFC28 H28 O2 SP 21 21 216.0742; 8.6056; 43.665
90; 90; 90		2282.5Chen, Jian-Ping; Xu, Ming-Hua
Chiral diene-promoted room temperature conjugate arylation: highly enantioselective synthesis of substituted chiral phenylalanine derivatives and α,α-di(arylmethyl)acetates.
Organic & biomolecular chemistry, 2020, 18, 4569-4574
7157428 CIFC26 H24 N2 O2P -19.778; 10.6122; 11.1756
103.043; 104.128; 92.353		1089.87Li, Ming; Yao, Tian-Yu; Sun, Sheng-Zheng; Yan, Ting-Xun; Wen, Li-Rong; Zhang, Lin-Bao
The ruthenium(ii)-catalyzed C-H olefination of indoles with alkynes: the facile construction of tetrasubstituted alkenes under aqueous conditions.
Organic & biomolecular chemistry, 2020, 18, 3158-3163
7157431 CIFC32 H33 N5 O4 SP 1 21/c 18.3154; 20.34; 17.962
90; 101.759; 90		2974.2Rong, Jing; Jiang, Hao; Wang, Sijing; Su, Zhenni; Wang, Huiyan; Tao, Chuanzhou
Metal-free cascade reactions of aziridines with arylalkynes and aryldiazoniums: facile access to arylazopyrrolines.
Organic & biomolecular chemistry, 2020, 18, 3149-3157
7157432 CIFC32 H29 Cl0 N3 O4 SP 1 21/c 114.818; 11.92; 16.557
90; 91.828; 90		2923Rong, Jing; Jiang, Hao; Wang, Sijing; Su, Zhenni; Wang, Huiyan; Tao, Chuanzhou
Metal-free cascade reactions of aziridines with arylalkynes and aryldiazoniums: facile access to arylazopyrrolines.
Organic & biomolecular chemistry, 2020, 18, 3149-3157
7157433 CIFC19 H26 N2 O2P 21 21 216.0543; 8.5333; 34.582
90; 90; 90		1786.6Pan, Changduo; Huang, Gao; Shan, Yujia; Li, Yiting; Yu, Jin-Tao
Rh(iii)-Catalyzed regioselective C4 alkylation of indoles with allylic alcohols: direct access to β-indolyl ketones.
Organic & biomolecular chemistry, 2020, 18, 3038-3042
7157434 CIFC27 H28 Cl2 F2 N4 SiP 1 21/c 114.1097; 10.9238; 17.0344
90; 94.326; 90		2618.06Furuta, Shohei; Mori, Toshiaki; Yoshigoe, Yusuke; Sekine, Kohei; Kuninobu, Yoichiro
Synthesis, structures and photophysical properties of hexacoordinated organosilicon compounds with 2-(2-pyridyl)phenyl groups.
Organic & biomolecular chemistry, 2020, 18, 3239-3242
7157435 CIFC23 H18 Cl2 F2 N2 SiP 1 21/c 19.0006; 16.2355; 14.0783
90; 96.804; 90		2042.76Furuta, Shohei; Mori, Toshiaki; Yoshigoe, Yusuke; Sekine, Kohei; Kuninobu, Yoichiro
Synthesis, structures and photophysical properties of hexacoordinated organosilicon compounds with 2-(2-pyridyl)phenyl groups.
Organic & biomolecular chemistry, 2020, 18, 3239-3242
7157436 CIFC24 H14 F8 N2 SiP -17.8983; 10.1395; 14.2203
80.924; 74.043; 85.365		1080.4Furuta, Shohei; Mori, Toshiaki; Yoshigoe, Yusuke; Sekine, Kohei; Kuninobu, Yoichiro
Synthesis, structures and photophysical properties of hexacoordinated organosilicon compounds with 2-(2-pyridyl)phenyl groups.
Organic & biomolecular chemistry, 2020, 18, 3239-3242
7157437 CIFC19 H14 Cl N O3 SP 1 21 15.5623; 8.7434; 17.6707
90; 96.868; 90		853.22Wang, Mei-Xin; Liu, Juan; Liu, Zhen; Wang, Yingcheng; Yang, Qi-Qiong; Shan, Wenyu; Deng, Yu-Hua; Shao, Zhihui
Enantioselective synthesis of chiral α-alkynylated thiazolidones by tandem S-addition/acetalization of alkynyl imines.
Organic & biomolecular chemistry, 2020, 18, 3117-3124
7157438 CIFC15 H15 Br N4 O3P -15.5984; 11.093; 12.6395
93.034; 97.303; 99.705		765.22Pretze, Marc; Neuber, Christin; Kinski, Elisa; Belter, Birgit; Köckerling, Martin; Caflisch, Amedeo; Steinbach, Jörg; Pietzsch, Jens; Mamat, Constantin
Synthesis, radiolabelling and initial biological characterisation of <sup>18</sup>F-labelled xanthine derivatives for PET imaging of Eph receptors.
Organic & biomolecular chemistry, 2020, 18, 3104-3116
7157439 CIFC10 H24 N4 O4P 1 21/c 110.3; 7.5991; 9.0926
90; 95.806; 90		708.03Pretze, Marc; Neuber, Christin; Kinski, Elisa; Belter, Birgit; Köckerling, Martin; Caflisch, Amedeo; Steinbach, Jörg; Pietzsch, Jens; Mamat, Constantin
Synthesis, radiolabelling and initial biological characterisation of <sup>18</sup>F-labelled xanthine derivatives for PET imaging of Eph receptors.
Organic & biomolecular chemistry, 2020, 18, 3104-3116
7157440 CIFC22 H18 N2 SP 1 21 19.768; 5.0226; 17.193
90; 95.43; 90		839.7Jiang, Jingjing; Tuo, Xiaolong; Fu, Zhuquan; Huang, Huawen; Deng, Guo-Jun
Three-component synthesis of 1,4-benzothiazines via iodide-catalyzed aerobic C-H sulfuration with elemental sulfur.
Organic & biomolecular chemistry, 2020, 18, 3234-3238
7157441 CIFC22 H16 N2 O2P 1 21/n 15.6311; 16.1768; 18.5883
90; 90.132; 90		1693.3Arcadi, Antonio; Aschi, Massimiliano; Chiarini, Marco; Marinelli, Fabio; Marsicano, Vincenzo; Portalone, Gustavo
Experimental results and computational insight into sequential reactions of β-(2-aminophenyl)-α,β-ynones with aryl isocyanates/benzoyl isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3177-3189
7157442 CIFC23 H18 N2 O2P 1 21/c 119.7918; 8.177; 24.1081
90; 107.785; 90		3715.14Arcadi, Antonio; Aschi, Massimiliano; Chiarini, Marco; Marinelli, Fabio; Marsicano, Vincenzo; Portalone, Gustavo
Experimental results and computational insight into sequential reactions of β-(2-aminophenyl)-α,β-ynones with aryl isocyanates/benzoyl isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3177-3189
7157443 CIFC24 H18 N2 O2 SP 21 21 216.576; 16.9049; 17.5937
90; 90; 90		1955.83Arcadi, Antonio; Aschi, Massimiliano; Chiarini, Marco; Marinelli, Fabio; Marsicano, Vincenzo; Portalone, Gustavo
Experimental results and computational insight into sequential reactions of β-(2-aminophenyl)-α,β-ynones with aryl isocyanates/benzoyl isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3177-3189
7157444 CIFC20 H16 Br2 O2 S3P 1 21/n 114.1114; 5.6423; 25.433
90; 98.033; 90		2005.1Jannapu Reddy, Raju; Waheed, Md; Rama Krishna, Gamidi
Phenylboronic acid-catalyzed tandem construction of S-S and C-S bonds: a new method for the synthesis of benzyl disulfanylsulfone derivatives from S-benzyl thiosulfonates.
Organic & biomolecular chemistry, 2020, 18, 3243-3248
7157445 CIFC22 H17 N2 O3P 1 21/c 19.8538; 10.2156; 18.572
90; 102.789; 90		1823.1Dagar, Anuradha; Seo, Yohan; Namkung, Wan; Kim, Ikyon
A domino annulation approach to 3,4-diacylpyrrolo[1,2-a]pyrazines: decoration of pyrazine units.
Organic & biomolecular chemistry, 2020, 18, 3324-3333
7157446 CIFC17 H15 N O2 SP -17.3519; 7.7182; 13.473
90.118; 98.358; 94.483		754Antony Savarimuthu, S.; Leo Prakash, D. G.; Augustine Thomas, S.; Gandhi, Thirumanavelan; Bera, Mrinal K.
Highly Z-selective synthesis of 1,3-oxathiol-2-ylidenes and 4-methylene-oxazolidine-2-thiones via atom-specific 5-exo-dig cyclization of propargyl alcohol with isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3552-3562
7157447 CIFC22 H16 Cl N O SP -19.729; 9.766; 10.945
67.938; 81.05; 73.602		923.1Antony Savarimuthu, S.; Leo Prakash, D. G.; Augustine Thomas, S.; Gandhi, Thirumanavelan; Bera, Mrinal K.
Highly Z-selective synthesis of 1,3-oxathiol-2-ylidenes and 4-methylene-oxazolidine-2-thiones via atom-specific 5-exo-dig cyclization of propargyl alcohol with isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3552-3562
7157448 CIFC17 H13 Cl2 N O SP 1 21/c 17.656; 21.804; 10.011
90; 106.066; 90		1605.9Antony Savarimuthu, S.; Leo Prakash, D. G.; Augustine Thomas, S.; Gandhi, Thirumanavelan; Bera, Mrinal K.
Highly Z-selective synthesis of 1,3-oxathiol-2-ylidenes and 4-methylene-oxazolidine-2-thiones via atom-specific 5-exo-dig cyclization of propargyl alcohol with isothiocyanate.
Organic & biomolecular chemistry, 2020, 18, 3552-3562
7157449 CIFC25 H20 Cl N O3 SP 1 21/c 113.132; 8.2538; 20.537
90; 105.43; 90		2145.8Lu, Tianyu; Zhang, Xuange; Miao, Zhiwei
Synthesis of methylene cyclopropane-fused chromenes and dihydroquinolines by sequential [4 + 2]- and [1 + 2]-annulation.
Organic & biomolecular chemistry, 2020, 18, 3303-3311
7157450 CIFC25 H18 O3P -19.5548; 10.071; 10.634
100.86; 104.43; 105.69		917.5Lu, Tianyu; Zhang, Xuange; Miao, Zhiwei
Synthesis of methylene cyclopropane-fused chromenes and dihydroquinolines by sequential [4 + 2]- and [1 + 2]-annulation.
Organic & biomolecular chemistry, 2020, 18, 3303-3311
7157451 CIFC24 H16 O2C 1 2/c 129.831; 11.148; 14.9443
90; 133.61; 90		3598.4Wu, Xinjie; Jia, Ming; Huang, Mengmeng; Kim, Jung Keun; Zhao, Zheng; Liu, Junkai; Xi, Jinhu; Li, Yabo; Wu, Yangjie
A visible-light-induced "on-off" one-pot synthesis of 3-arylacetylene coumarins with AIE properties.
Organic & biomolecular chemistry, 2020, 18, 3346-3353
7157452 CIFC25 H18 O3P c a 2121.9993; 12.5762; 13.8028
90; 90; 90		3818.79Wu, Xinjie; Jia, Ming; Huang, Mengmeng; Kim, Jung Keun; Zhao, Zheng; Liu, Junkai; Xi, Jinhu; Li, Yabo; Wu, Yangjie
A visible-light-induced "on-off" one-pot synthesis of 3-arylacetylene coumarins with AIE properties.
Organic & biomolecular chemistry, 2020, 18, 3346-3353
7157453 CIFC24 H13 F3 O2P 1 21/c 111.8769; 11.865; 14.2912
90; 110.026; 90		1892.1Wu, Xinjie; Jia, Ming; Huang, Mengmeng; Kim, Jung Keun; Zhao, Zheng; Liu, Junkai; Xi, Jinhu; Li, Yabo; Wu, Yangjie
A visible-light-induced "on-off" one-pot synthesis of 3-arylacetylene coumarins with AIE properties.
Organic & biomolecular chemistry, 2020, 18, 3346-3353
7157454 CIFC24 H15 F O3P c a 2121.9897; 12.2777; 13.5508
90; 90; 90		3658.48Wu, Xinjie; Jia, Ming; Huang, Mengmeng; Kim, Jung Keun; Zhao, Zheng; Liu, Junkai; Xi, Jinhu; Li, Yabo; Wu, Yangjie
A visible-light-induced "on-off" one-pot synthesis of 3-arylacetylene coumarins with AIE properties.
Organic & biomolecular chemistry, 2020, 18, 3346-3353
7157455 CIFC23 H14 O2P -110.9195; 11.7513; 14.206
87.69; 77.763; 71.943		1693.1Wu, Xinjie; Jia, Ming; Huang, Mengmeng; Kim, Jung Keun; Zhao, Zheng; Liu, Junkai; Xi, Jinhu; Li, Yabo; Wu, Yangjie
A visible-light-induced "on-off" one-pot synthesis of 3-arylacetylene coumarins with AIE properties.
Organic & biomolecular chemistry, 2020, 18, 3346-3353
7157456 CIFC22 H28 O2 SiC 1 2 119.7751; 7.6977; 13.7091
90; 104.859; 90		2017.05Sarkar, Parantap; Inaba, Yuya; Shirakura, Hayato; Yoneda, Tomoki; Inokuma, Yasuhide
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Organic & biomolecular chemistry, 2020, 18, 3297-3302
7157457 CIFC20 H30 O4P 1 21/n 19.8166; 12.8538; 14.9915
90; 98.444; 90		1871.13Sarkar, Parantap; Inaba, Yuya; Shirakura, Hayato; Yoneda, Tomoki; Inokuma, Yasuhide
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Organic & biomolecular chemistry, 2020, 18, 3297-3302
7157458 CIFC10 H19 O2 SiP 1 21/c 17.1033; 15.7; 10.748
90; 90.224; 90		1198.6Sarkar, Parantap; Inaba, Yuya; Shirakura, Hayato; Yoneda, Tomoki; Inokuma, Yasuhide
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Organic & biomolecular chemistry, 2020, 18, 3297-3302
7157459 CIFC34 H50 O8P -17.0479; 10.1584; 11.6894
91.402; 99.676; 96.997		817.99Sarkar, Parantap; Inaba, Yuya; Shirakura, Hayato; Yoneda, Tomoki; Inokuma, Yasuhide
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Organic & biomolecular chemistry, 2020, 18, 3297-3302
7157460 CIFC34 H50 O8P -17.3875; 9.2832; 11.5913
103.164; 95.845; 95.145		764.77Sarkar, Parantap; Inaba, Yuya; Shirakura, Hayato; Yoneda, Tomoki; Inokuma, Yasuhide
Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives.
Organic & biomolecular chemistry, 2020, 18, 3297-3302
7157461 CIFC27 H33 N OP 1 21/n 19.317; 18.704; 13.6865
90; 93.967; 90		2379.4Rayaroth, Amritha; Singh, Rajat Kumar; A V, Kalyanakrishnan; Hari, Krishna; Kaliyamoorthy, Alagiri
Base-promoted 1,6-conjugate addition of alkylazaarenes to para-quinone methides.
Organic & biomolecular chemistry, 2020, 18, 3354-3359
7157462 CIFC20 H14 Cl NP -15.5878; 10.8004; 13.7039
105.531; 91.027; 101.719		777.93Fang, Benyao; Hou, Jiao; Tian, Jinyue; Yu, Wenquan; Chang, Junbiao
Synthesis of phenanthridines by I<sub>2</sub>-mediated sp<sup>3</sup> C-H amination.
Organic & biomolecular chemistry, 2020, 18, 3312-3323
7157463 CIFC31 H32 Br N3 O6P 1 21/n 18.3958; 10.3211; 33.5425
90; 91.208; 90		2905.94Ao, Chaoqun; Huang, Jingjing; Xu, Xinfang; Jia, Shikun; Kang, Zhenghui; Hu, Wenhao
A Rh-catalyzed three-component reaction for the diastereoselective synthesis of pyrazolone derivatives with contiguous quaternary stereocenters.
Organic & biomolecular chemistry, 2020, 18, 3466-3470
7157464 CIFC22 H18 O2P 1 21/c 18.6541; 5.7809; 33.543
90; 97.281; 90		1664.57Dos Santos, Emerson E. F.; de Souza, Gabriela F. P.; Simoni, Deborah A.; Salles, Jr, Airton G
A base-promoted tandem approach to bicyclic 8-membered ring ketones.
Organic & biomolecular chemistry, 2020, 18, 3249-3253
7157465 CIFC26 H22 N4 O2 SP c a 2111.5618; 20.0595; 20.7439
90; 90; 90		4811Yang, Zhen; He, Jing; Wei, Yueting; Li, Weiwei; Liu, Ping
KI/TBHP-promoted [3 + 2] cycloaddition of pyrrolo[1,2-a]quinoxalines and N-arylsulfonylhydrazones.
Organic & biomolecular chemistry, 2020, 18, 3360-3366
7157466 CIFC16 H11 N5 O2P 1 21 17.1117; 14.251; 7.5497
90; 102.83; 90		746Kim, Woo Gyum; Baek, Seung-Yeol; Jeong, Seo Yeong; Nam, Dongsik; Jeon, Ji Hwan; Choe, Wonyoung; Baik, Mu-Hyun; Hong, Sung You
Chemo- and regioselective click reactions through nickel-catalyzed azide-alkyne cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 3374-3381
7157467 CIFC19 H18 N4 O2P 1 21/c 19.6779; 15.962; 12.006
90; 108.7; 90		1756.8Kim, Woo Gyum; Baek, Seung-Yeol; Jeong, Seo Yeong; Nam, Dongsik; Jeon, Ji Hwan; Choe, Wonyoung; Baik, Mu-Hyun; Hong, Sung You
Chemo- and regioselective click reactions through nickel-catalyzed azide-alkyne cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 3374-3381
7157468 CIFC19 H18 N4 O3P b c a14.942; 12.891; 17.93
90; 90; 90		3453.6Kim, Woo Gyum; Baek, Seung-Yeol; Jeong, Seo Yeong; Nam, Dongsik; Jeon, Ji Hwan; Choe, Wonyoung; Baik, Mu-Hyun; Hong, Sung You
Chemo- and regioselective click reactions through nickel-catalyzed azide-alkyne cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 3374-3381
7157469 CIFC28 H23 N3 SP b c a13.151; 18.198; 19.461
90; 90; 90		4657.4Kim, Woo Gyum; Baek, Seung-Yeol; Jeong, Seo Yeong; Nam, Dongsik; Jeon, Ji Hwan; Choe, Wonyoung; Baik, Mu-Hyun; Hong, Sung You
Chemo- and regioselective click reactions through nickel-catalyzed azide-alkyne cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 3374-3381
7157470 CIFC14 H10 Br N O2P 1 21/c 113.7872; 11.4491; 7.3967
90; 101.273; 90		1145.05Calatrava-Pérez, Elena; Acherman, Stefan; Stricker, Lucas; McManus, Gavin; Delente, Jason; Lynes, Amy D.; Henwood, Adam F.; Lovitt, June I.; Hawes, Chris S.; Byrne, Kevin; Schmitt, Wolfgang; Kotova, Oxana; Gunnlaugsson, Thorfinnur; Scanlan, Eoin M.
Fluorescent supramolecular hierarchical self-assemblies from glycosylated 4-amino- and 4-bromo-1,8-naphthalimides.
Organic & biomolecular chemistry, 2020, 18, 3475-3480
7157471 CIFC20 H22 Br N O2P -14.6972; 11.9618; 15.7954
81.534; 86.654; 84.89		873.41Calatrava-Pérez, Elena; Acherman, Stefan; Stricker, Lucas; McManus, Gavin; Delente, Jason; Lynes, Amy D.; Henwood, Adam F.; Lovitt, June I.; Hawes, Chris S.; Byrne, Kevin; Schmitt, Wolfgang; Kotova, Oxana; Gunnlaugsson, Thorfinnur; Scanlan, Eoin M.
Fluorescent supramolecular hierarchical self-assemblies from glycosylated 4-amino- and 4-bromo-1,8-naphthalimides.
Organic & biomolecular chemistry, 2020, 18, 3475-3480
7157472 CIFC32 H28 Br2 N2 O4P -14.4247; 16.1174; 19.4957
99.692; 94.484; 92.775		1363.61Calatrava-Pérez, Elena; Acherman, Stefan; Stricker, Lucas; McManus, Gavin; Delente, Jason; Lynes, Amy D.; Henwood, Adam F.; Lovitt, June I.; Hawes, Chris S.; Byrne, Kevin; Schmitt, Wolfgang; Kotova, Oxana; Gunnlaugsson, Thorfinnur; Scanlan, Eoin M.
Fluorescent supramolecular hierarchical self-assemblies from glycosylated 4-amino- and 4-bromo-1,8-naphthalimides.
Organic & biomolecular chemistry, 2020, 18, 3475-3480
7157473 CIFC18 H18 O3 SP 1 21/n 15.5466; 9.9811; 27.5422
90; 91.085; 90		1524.5Lin, Qifu; Yao, Yongqi; Yang, Wen; Tan, Yun; Chen, Shuqi; Chen, Donghan; Yang, Dingqiao
Copper-catalyzed diastereoselective hydrothioetherification of oxa(aza)benzonorbornadienes.
Organic & biomolecular chemistry, 2020, 18, 3575-3584
7157474 CIFC35 H32 N2 O5P -110.5718; 10.6288; 13.5806
100.473; 97.068; 103.526		1436.9Zhulanov, Vladimir E.; Vigovskaya, Valeria A.; Dmitriev, Maksim V.; Silaichev, Pavel S.; Maslivets, Andrey N.; Rubin, Michael
Dipyrazolodioxadiazocines as shelf-stable "ready-to-use" precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines.
Organic & biomolecular chemistry, 2020, 18, 3382-3391
7157475 CIFC66 H66 N4 O11P -19.2689; 9.782; 35.199
94.886; 92.57; 115.038		2869.4Zhulanov, Vladimir E.; Vigovskaya, Valeria A.; Dmitriev, Maksim V.; Silaichev, Pavel S.; Maslivets, Andrey N.; Rubin, Michael
Dipyrazolodioxadiazocines as shelf-stable "ready-to-use" precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines.
Organic & biomolecular chemistry, 2020, 18, 3382-3391
7157476 CIFC21 H26 Br Cl F6 N2 P Rh SeP -19.3467; 11.887; 11.887
97.25; 97.072; 97.072		1287.2Sharma, Charu; Srivastava, Avinash Kumar; Sharma, Kamal Nayan; Joshi, Raj Kumar
Half-sandwich (η<sup>5</sup>-Cp*)Rh(iii) complexes of pyrazolated organo-sulfur/selenium/tellurium ligands: efficient catalysts for base/solvent free C-N coupling of chloroarenes under aerobic conditions.
Organic & biomolecular chemistry, 2020, 18, 3599-3606
7157477 CIFC21 H26 Br Cl F6 N2 P Rh SC 1 c 112.562; 11.151; 19.041
90; 91.874; 90		2665.8Sharma, Charu; Srivastava, Avinash Kumar; Sharma, Kamal Nayan; Joshi, Raj Kumar
Half-sandwich (η<sup>5</sup>-Cp*)Rh(iii) complexes of pyrazolated organo-sulfur/selenium/tellurium ligands: efficient catalysts for base/solvent free C-N coupling of chloroarenes under aerobic conditions.
Organic & biomolecular chemistry, 2020, 18, 3599-3606
7157478 CIFC23 H16 F3 N O2 SeP 1 21/c 15.7568; 25.3971; 13.5914
90; 98.147; 90		1967.1Recchi, Ana Maria S.; Rosa, Pedro H. P.; Back, Davi F.; Zeni, Gilson
Selenium-promoted electrophilic cyclization of arylpropiolamides: synthesis of 3-organoselenyl spiro[4,5]trienones.
Organic & biomolecular chemistry, 2020, 18, 3544-3551
7157479 CIFC44 H34 N2 O4 Se2P 1 c 19.6477; 14.9116; 13.3181
90; 98.129; 90		1896.73Recchi, Ana Maria S.; Rosa, Pedro H. P.; Back, Davi F.; Zeni, Gilson
Selenium-promoted electrophilic cyclization of arylpropiolamides: synthesis of 3-organoselenyl spiro[4,5]trienones.
Organic & biomolecular chemistry, 2020, 18, 3544-3551
7157480 CIFC40 H32 N0 O12F d d 218.987; 25.021; 7.087
90; 90; 90		3366.8Roy, Biswajit; Das, Eshani; Roy, Avijit; Mal, Dipakranjan
Ni(ii)-Catalyzed vinylic C-H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids.
Organic & biomolecular chemistry, 2020, 18, 3697-3706
7157481 CIFC11 H10 O3P 1 21 17.57; 9.753; 13.656
90; 102.23; 90		985.3Roy, Biswajit; Das, Eshani; Roy, Avijit; Mal, Dipakranjan
Ni(ii)-Catalyzed vinylic C-H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids.
Organic & biomolecular chemistry, 2020, 18, 3697-3706
7157482 CIFC80 H56 N8 O40C 1 2/c 125.689; 10.003; 7.418
90; 105.62; 90		1835.8Roy, Biswajit; Das, Eshani; Roy, Avijit; Mal, Dipakranjan
Ni(ii)-Catalyzed vinylic C-H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids.
Organic & biomolecular chemistry, 2020, 18, 3697-3706
7157483 CIFC11 H7 N O3P -18.009; 9.607; 13.044
94.77; 105.91; 108.25		900.812Roy, Biswajit; Das, Eshani; Roy, Avijit; Mal, Dipakranjan
Ni(ii)-Catalyzed vinylic C-H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids.
Organic & biomolecular chemistry, 2020, 18, 3697-3706
7157484 CIFC22 H23 Cl N2 O3C 1 2 124.1998; 12.37; 9.5879
90; 119.944; 90		2487Cui, Hao; Li, Ke; Wang, Yue; Song, Manman; Wang, Congcong; Wei, Donghui; Li, Er-Qing; Duan, Zheng; Mathey, François
Copper(i)/Ganphos catalysis: enantioselective synthesis of diverse spirooxindoles using iminoesters and alkyl substituted methyleneindolinones.
Organic & biomolecular chemistry, 2020, 18, 3740-3746
7157485 CIFC30 H52 O4P 21 21 216.61847; 9.54; 44.1844
90; 90; 90		2789.81Xiao, Long-Gao; Zhang, Yu; Zhang, Hong-Li; Li, Ding; Gu, Qiong; Tang, Gui-Hua; Yu, Qian; An, Lin-Kun
Spiroconyone A, a new phytosterol with a spiro [5,6] ring system from Conyza japonica.
Organic & biomolecular chemistry, 2020, 18, 5130-5136
7157486 CIFC16 H11 Br N O2P -18.3268; 9.2126; 9.6765
83.964; 73.197; 73.333		680.55Sreedharan, Ramdas; Rajeshwaran, Purushothaman; Panyam, Pradeep Kumar Reddy; Yadav, Saurabh; Nagaraja, C. M.; Gandhi, Thirumanavelan
Acylation of oxindoles using methyl/phenyl esters via the mixed Claisen condensation - an access to 3-alkylideneoxindoles.
Organic & biomolecular chemistry, 2020, 18, 3843-3847
7157487 CIFC17 H14 N O3P 1 21/c 111.1312; 8.2115; 16.7219
90; 109.192; 90		1443.5Sreedharan, Ramdas; Rajeshwaran, Purushothaman; Panyam, Pradeep Kumar Reddy; Yadav, Saurabh; Nagaraja, C. M.; Gandhi, Thirumanavelan
Acylation of oxindoles using methyl/phenyl esters via the mixed Claisen condensation - an access to 3-alkylideneoxindoles.
Organic & biomolecular chemistry, 2020, 18, 3843-3847
7157488 CIFC16 H10 Cl F12 N O3P 1 21/c 17.7099; 16.5285; 15.8165
90; 94.189; 90		2010.2Mo, Zu-Yu; Wang, Xin-Yu; Zhang, Yu-Zhen; Yang, Li; Tang, Hai-Tao; Pan, Ying-Ming
Electrochemically enabled functionalization of indoles or anilines for the synthesis of hexafluoroisopropoxy indole and aniline derivatives.
Organic & biomolecular chemistry, 2020, 18, 3832-3837
7157489 CIFC210 H270 B6 N6 O24C 1 2/m 142.922; 30.652; 19.133
90; 94.97; 90		25078Danjo, Hiroshi; Masuda, Yuhki; Kidena, Yuki; Kawahata, Masatoshi; Ohara, Kazuaki; Yamaguchi, Kentaro
Preparation of cage-shaped hexakis(spiroborate)s.
Organic & biomolecular chemistry, 2020, 18, 3717-3723
7157490 CIFC223.49 H272.13 B6 N6.66 O25.16P -127.909; 32.78; 34.958
105.11; 107.86; 110.03		26098Danjo, Hiroshi; Masuda, Yuhki; Kidena, Yuki; Kawahata, Masatoshi; Ohara, Kazuaki; Yamaguchi, Kentaro
Preparation of cage-shaped hexakis(spiroborate)s.
Organic & biomolecular chemistry, 2020, 18, 3717-3723
7157491 CIFC45 H74 N2 O20 S2P 43 21 29.74142; 9.74142; 55.7588
90; 90; 90		5291.25Tota, Arianna; Carlucci, Claudia; Pisano, Luisa; Cutolo, Giuliano; Clarkson, Guy J.; Romanazzi, Giuseppe; Degennaro, Leonardo; Bull, James A.; Rollin, Patrick; Luisi, Renzo
Synthesis of glycosyl sulfoximines by a highly chemo- and stereoselective NH- and O-transfer to thioglycosides.
Organic & biomolecular chemistry, 2020, 18, 3893-3897
7157492 CIFC25 H17 Cl O4C 1 2 117.9619; 9.8922; 22.6104
90; 96.832; 90		3988.95Yang, Xiao-Chao; Xu, Meng; Wang, Jin-Bao; Liu, Meng-Meng; Mathey, François; Hua, Yuan-Zhao; Wang, Min-Can
Enantioselective synthesis of indanone spiro-isochromanone derivatives via a dinuclear zinc-catalyzed Michael/transesterification tandem reaction.
Organic & biomolecular chemistry, 2020, 18, 3917-3926
7157493 CIFC24 H19 N O6P -18.2622; 10.8562; 11.4554
83.258; 82.82; 84.193		1008.49Ravindran, Jaice; Yadhukrishnan, Velickakathu O.; Asha, Reghuvaran S.; Lankalapalli, Ravi S.
Dienaminodioate based multicomponent reactions with post-benzylic oxidative transformations mediated by DDQ.
Organic & biomolecular chemistry, 2020, 18, 3927-3937
7157494 CIFC33 H30 Cl N3 O9P -19.3935; 10.3136; 17.8351
102.592; 95.138; 101.978		1633.08Ravindran, Jaice; Yadhukrishnan, Velickakathu O.; Asha, Reghuvaran S.; Lankalapalli, Ravi S.
Dienaminodioate based multicomponent reactions with post-benzylic oxidative transformations mediated by DDQ.
Organic & biomolecular chemistry, 2020, 18, 3927-3937
7157495 CIFC22 H32 O4P 1 21 112.5521; 6.6052; 12.9824
90; 113.567; 90		986.58Zou, Chun-Xin; Hou, Zi-Lin; Bai, Ming; Guo, Rui; Lin, Bin; Wang, Xiao-Bo; Huang, Xiao-Xiao; Song, Shao-Jiang
Highly modified steroids from Inonotus obliquus.
Organic & biomolecular chemistry, 2020, 18, 3908-3916
7157496 CIFC24 H34.5 O17.25C 1 2 119.2032; 6.11; 10.9617
90; 103.271; 90		1251.81St-Gelais, Jacob; Denavit, Vincent; Giguère, Denis
Efficient synthesis of a galectin inhibitor clinical candidate (TD139) using a Payne rearrangement/azidation reaction cascade.
Organic & biomolecular chemistry, 2020, 18, 3903-3907
7157497 CIFC17 H11 N O3 S2P 21 21 216.4978; 14.5164; 16.2262
90; 90; 90		1530.5Mondal, Santa; Mahato, Karuna; Arora, Neha; Kankane, Dheerendra; Singh, Umed Pratap; Ali, Saghir; Khan, Aftab Hossain; Ghosh, Siddhartha S.; Khan, Abu T.
Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity.
Organic & biomolecular chemistry, 2020, 18, 4104-4113
7157498 CIFC17 H11 N O S2C 1 2/c 117.5086; 11.7781; 13.9721
90; 92.715; 90		2878.1Mondal, Santa; Mahato, Karuna; Arora, Neha; Kankane, Dheerendra; Singh, Umed Pratap; Ali, Saghir; Khan, Aftab Hossain; Ghosh, Siddhartha S.; Khan, Abu T.
Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity.
Organic & biomolecular chemistry, 2020, 18, 4104-4113
7157499 CIFC30 H29 N O7P 1 21/n 111.695; 14.5145; 15.6982
90; 107.486; 90		2541.59Cui, Hai-Lei
FeCl<sub>2</sub> catalyzed direct modification of dihydropyrrolo[2,1-a]isoquinolines with phenols.
Organic & biomolecular chemistry, 2020, 18, 4085-4089
7157500 CIFC57 H77 N O6P 21 21 2112.008; 13.0066; 34.139
90; 90; 90		5331.9Peng, Xiaogang; Duan, Fangfang; He, Yangzhou; Gao, Ying; Chen, Juan; Chang, Jinling; Ruan, Hanli
Ergocytochalasin A, a polycyclic merocytochalasan from an endophytic fungus Phoma multirostrata XJ-2-1.
Organic & biomolecular chemistry, 2020, 18, 4056-4062
7157501 CIFC8 H12 F N O4 SP -16.9928; 7.7011; 10.3093
79.651; 81.793; 80.005		534.28Liu, Jing; Wang, Shi-Meng; Qin, Hua-Li
Light-induced [2 + 2] cycloadditions for the construction of cyclobutane-fused pyridinyl sulfonyl fluorides.
Organic & biomolecular chemistry, 2020, 18, 4019-4023
7157502 CIFC26 H24 N2 O2 SP 43 21 29.3559; 9.3559; 60.611
90; 90; 90		5305.5Yang, Junxian; He, Zeyuan; Hong, Liang; Sun, Wangsheng; Wang, Rui
Asymmetric N-aminoalkylation of 3-substituted indoles by N-protected N,O-acetals: an access to chiral propargyl aminals.
Organic & biomolecular chemistry, 2020, 18, 4169-4173
7157503 CIFC14 H18 B N O2P b c a10.372; 12.8487; 21.0007
90; 90; 90		2798.69Zhao, Jia-Hui; Zhou, Zhao-Zhao; Zhang, Yue; Su, Xuan; Chen, Xi-Meng; Liang, Yong-Min
Visible-light-mediated borylation of aryl and alkyl halides with a palladium complex.
Organic & biomolecular chemistry, 2020, 18, 4390-4394
7157504 CIFC16 H13 Cl N2 OP c c n8.947; 16.934; 18.608
90; 90; 90		2819.3Hu, Fang-Peng; Cui, Xin-Feng; Lu, Guo-Qiang; Huang, Guo-Sheng
Base-promoted Lewis acid catalyzed synthesis of quinazoline derivatives.
Organic & biomolecular chemistry, 2020, 18, 4376-4380
7157505 CIFC16 H14 N2 O2P -14.9529; 11.1696; 13.2334
112.623; 99.49; 94.354		658.67Yang, Huiyong; Xu, Jun; Zhang, Yilan; He, Lei; Zhang, Pengfei; Li, Wanmei
Synthesis of quinazoin-4-ones through an acid ion exchange resin mediated cascade reaction.
Organic & biomolecular chemistry, 2020, 18, 4406-4414
7157506 CIFC19 H23 Br N2P 1 21/c 119.7432; 18.485; 10.3179
90; 99.181; 90		3717.3Banerjee, Indrani; Sagar, Shweta; Panda, Tarun K.
Calcium mediated efficient synthesis of N-arylamidines from organic nitriles and amines.
Organic & biomolecular chemistry, 2020, 18, 4231-4237
7157507 CIFC26 H28 Cl N3 OP 1 21/n 112.988; 15.255; 14.374
90; 104.275; 90		2760Banerjee, Indrani; Sagar, Shweta; Panda, Tarun K.
Calcium mediated efficient synthesis of N-arylamidines from organic nitriles and amines.
Organic & biomolecular chemistry, 2020, 18, 4231-4237
7157508 CIFC21 H29 N3P 1 21/n 18.5523; 10.6764; 20.418
90; 93.693; 90		1860.5Banerjee, Indrani; Sagar, Shweta; Panda, Tarun K.
Calcium mediated efficient synthesis of N-arylamidines from organic nitriles and amines.
Organic & biomolecular chemistry, 2020, 18, 4231-4237
7157509 CIFC27 H30 Cl N3 O2P 1 21/n 118.7816; 29.0379; 19.9928
90; 115.493; 90		9842Banerjee, Indrani; Sagar, Shweta; Panda, Tarun K.
Calcium mediated efficient synthesis of N-arylamidines from organic nitriles and amines.
Organic & biomolecular chemistry, 2020, 18, 4231-4237
7157510 CIFC14 H23 Cl N2 O2P 1 21/c 113.9531; 18.3735; 12.488
90; 90.003; 90		3201.5He, Xinwei; Yang, Cheng; Wu, Yinsong; Xie, Mengqing; Li, Ruxue; Duan, Jiahui; Shang, Yongjia
Synthesis of unsymmetrical urea derivatives via one-pot sequential three-component reactions of cyclic 2-diazo-1,3-diketones, carbodiimides, and 1,2-dihaloethanes.
Organic & biomolecular chemistry, 2020, 18, 4178-4182
7157511 CIFC14 H10 N2 O2 SP 1 21/c 112.7318; 9.1027; 20.8094
90; 96.677; 90		2395.3Singh, Manpreet; Vaishali, ?; Paul, Avijit Kumar; Singh, Virender
Isatin as a 2-aminobenzaldehyde surrogate: transition metal-free efficient synthesis of 2-(2'-aminophenyl)benzothiazole derivatives.
Organic & biomolecular chemistry, 2020, 18, 4459-4469
7157512 CIFC14 H11 N S2P n a 2127.604; 7.7285; 5.8633
90; 90; 90		1250.86Wang, Dungai; Liang, Xiao; Xiong, Mingteng; Zhu, Heping; Zhou, Yifeng; Pan, Yuanjiang
Synthesis of unsymmetrical disulfides via PPh<sub>3</sub>-mediated reductive coupling of thiophenols with sulfonyl chlorides.
Organic & biomolecular chemistry, 2020, 18, 4447-4451
7157513 CIFC15 H18 B F2 N O2 SP b c a8.2789; 13.5084; 29.7538
90; 90; 90		3327.5Wei, Jun; Bao, Kun; Wang, Yuan; Sheng, Rong; Hu, Jinbo
Novel usage of 2-BTSO<sub>2</sub>CF<sub>2</sub>H for metal-free electrophilic difluoroalkanethiolation of indoles.
Organic & biomolecular chemistry, 2020, 18, 4556-4559
7157514 CIFC59 H59 B F2 N4 O6C 1 2/c 127.487; 11.9733; 19.9835
90; 132.48; 90		4850.5Sugiura, Shinya; Maeda, Hiromitsu
Pyrrole-based anion-responsive π-electronic molecules as fluorescence sensors responsive to multiple stimuli.
Organic & biomolecular chemistry, 2020, 18, 4433-4438
7157515 CIFC28 H25 N O6P -110.6091; 11.9396; 20.1405
103.598; 99.511; 95.686		2420.12Luo, Si-Qin; Liu, Wei; Ruan, Ban-Feng; Fan, Shi-Lu; Zhu, Hui-Xia; Tao, Wei; Xiao, Hua
P(NMe<sub>2</sub>)<sub>3</sub> mediated cyclopropanation of α-methylene-β-lactams for rapid syntheses of spirocyclopropyl β-lactams.
Organic & biomolecular chemistry, 2020, 18, 4599-4603
7157516 CIFC25 H20 Br N O3P -19.6348; 10.2842; 11.504
103.149; 104.108; 94.618		1065.31Luo, Si-Qin; Liu, Wei; Ruan, Ban-Feng; Fan, Shi-Lu; Zhu, Hui-Xia; Tao, Wei; Xiao, Hua
P(NMe<sub>2</sub>)<sub>3</sub> mediated cyclopropanation of α-methylene-β-lactams for rapid syntheses of spirocyclopropyl β-lactams.
Organic & biomolecular chemistry, 2020, 18, 4599-4603
7157517 CIFC192 H224 B6 F24 N8 O48P 42/n :225.0521; 25.0521; 15.1716
90; 90; 90		9521.8Martinez-Bulit, Pablo; Wilson, Benjamin H.; Loeb, Stephen J.
One-pot synthesis of porphyrin-based [5]rotaxanes.
Organic & biomolecular chemistry, 2020, 18, 4395-4400
7157518 CIFC22 H44 B10 O4P -110.486; 11.704; 13.581
87.493; 84.584; 66.838		1525.5Zhang, Chuyi; Wang, Qian; Tian, Song; Zhang, Jianwei; Li, Jiaoyi; Zhou, Ling; Lu, Jian
Palladium-catalyzed regioselective synthesis of B(4,5)- or B(4)-substituted o-carboranes containing α,β-unsaturated carbonyls.
Organic & biomolecular chemistry, 2020, 18, 4723-4727
7157519 CIFC32 H29 N O SP 1 21 19.25182; 14.2225; 10.38203
90; 106.464; 90		1310.1Li, Ying-Xian; Cheng, Cheng; Tang, Lei; Yang, Yuan-Yong
Palladium catalyzed asymmetric allylic alkylation of isoquinolinedione derivatives in the preparation of quaternary carbon stereocenters.
Organic & biomolecular chemistry, 2020, 18, 4551-4555
7157520 CIFC4.75 H5 N O1.25P 1 21/c 118.271; 8.4386; 12.378
90; 93.24; 90		1905.4Surendra Reddy, G.; Suresh Kumar, A.; Ramachary, Dhevalapally B.
Organocatalytic enone-azide [3 + 2]-cycloaddition: synthesis of functionally rich C/N-double vinyl 1,2,3-triazoles.
Organic & biomolecular chemistry, 2020, 18, 4470-4478
7157521 CIFC5.67 H6.33 N OP -17.2978; 8.2873; 14.1639
97.85; 94.308; 110.859		785.86Surendra Reddy, G.; Suresh Kumar, A.; Ramachary, Dhevalapally B.
Organocatalytic enone-azide [3 + 2]-cycloaddition: synthesis of functionally rich C/N-double vinyl 1,2,3-triazoles.
Organic & biomolecular chemistry, 2020, 18, 4470-4478
7157522 CIFC2 H2 Cl0.14 N0.43 O0.29P 1 21 16.5916; 4.0692; 26.512
90; 94.367; 90		709.1Surendra Reddy, G.; Suresh Kumar, A.; Ramachary, Dhevalapally B.
Organocatalytic enone-azide [3 + 2]-cycloaddition: synthesis of functionally rich C/N-double vinyl 1,2,3-triazoles.
Organic & biomolecular chemistry, 2020, 18, 4470-4478
7157523 CIFC8 H6 Br3 N O2P b c a7.016; 16.476; 19.291
90; 90; 90		2230Okuma, Kentaro; Qu, Yuxuan; Suetome, Aoi; Nagahora, Noriyoshi
Reaction of ketone hydrazones with TeCl<sub>4</sub>: isolation and reactions of novel divinyl telluride.
Organic & biomolecular chemistry, 2020, 18, 4583-4589
7157524 CIFC16 H12 Br2 N2 O4 TeC 1 2/c 115.726; 10.425; 13.63
90; 121.565; 90		1903.9Okuma, Kentaro; Qu, Yuxuan; Suetome, Aoi; Nagahora, Noriyoshi
Reaction of ketone hydrazones with TeCl<sub>4</sub>: isolation and reactions of novel divinyl telluride.
Organic & biomolecular chemistry, 2020, 18, 4583-4589
7157525 CIFC31 H33 N O3P 1 21/n 110.0037; 20.2706; 13.2122
90; 92.231; 90		2677.15You, Yong; Quan, Bao-Xue; Wang, Zhen-Hua; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Divergent synthesis of oxindole derivatives via controllable reactions of isatin-derived para-quinone methides with sulfur ylides.
Organic & biomolecular chemistry, 2020, 18, 4560-4565
7157526 CIFC31 H33 N O3P -19.4791; 9.7988; 15.518
83.644; 83.34; 62.855		1271.23You, Yong; Quan, Bao-Xue; Wang, Zhen-Hua; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Divergent synthesis of oxindole derivatives via controllable reactions of isatin-derived para-quinone methides with sulfur ylides.
Organic & biomolecular chemistry, 2020, 18, 4560-4565
7157527 CIFC96 H31 N O S2P 1 21/n 110.205; 23.555; 23.364
90; 95.62; 90		5589.21Yang, Yong; Niu, Chuang; Chen, Muqing; Yang, Shangfeng; Wang, Guan-Wu
Electrochemical regioselective alkylations of a [60]fulleroindoline with bulky alkyl bromides.
Organic & biomolecular chemistry, 2020, 18, 4783-4787
7157528 CIFC20 H21 F3 O2P 1 21/n 110.8717; 10.7087; 15.1761
90; 95.029; 90		1760.03Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Syntheses of α-CF<sub>3</sub>-α-quaternary ketones via p-quinone methides and their derivatization to compounds with successively congested stereogenic centers.
Organic & biomolecular chemistry, 2020, 18, 4638-4644
7157529 CIFC17 H17 F3 O2P b c n24.336; 7.1684; 16.7513
90; 90; 90		2922.3Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Syntheses of α-CF<sub>3</sub>-α-quaternary ketones via p-quinone methides and their derivatization to compounds with successively congested stereogenic centers.
Organic & biomolecular chemistry, 2020, 18, 4638-4644
7157530 CIFC26 H26 Cl F3 O4P 1 21/n 112.0518; 11.0358; 18.5393
90; 103.931; 90		2393.22Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Syntheses of α-CF<sub>3</sub>-α-quaternary ketones via p-quinone methides and their derivatization to compounds with successively congested stereogenic centers.
Organic & biomolecular chemistry, 2020, 18, 4638-4644
7157531 CIFC23 H21 F3 O4 SP 1 21/n 113.8943; 9.9889; 15.0537
90; 99.237; 90		2062.19Terashima, Kyu; Kawasaki-Takasuka, Tomoko; Agou, Tomohiro; Kubota, Toshio; Yamazaki, Takashi
Syntheses of α-CF<sub>3</sub>-α-quaternary ketones via p-quinone methides and their derivatization to compounds with successively congested stereogenic centers.
Organic & biomolecular chemistry, 2020, 18, 4638-4644
7157532 CIFC23 H18 O3 SeP 1 21 112.2311; 5.5378; 13.6984
90; 95.773; 90		923.13Sahoo, Sushree Ranjan; Sarkar, Debayan; Henkel, Felix; Reuter, Hans
Copper(i) catalyzed synthesis of selanyl methylene 4-chromanol and aurone derivatives.
Organic & biomolecular chemistry, 2020, 18, 4619-4627
7157533 CIFC20 H17 Br N2 O3P 1 21/c 116.6385; 14.3268; 7.7041
90; 100.731; 90		1804.4Shi, Yaqi; Yang, Fan; Wu, Yangjie
Palladium-catalyzed C8-H alkoxycarbonylation of 1-naphthylamines with alkyl chloroformates.
Organic & biomolecular chemistry, 2020, 18, 4628-4637
7157534 CIFC59 H56 Cl N3 O14 SP 1 21 15.2366; 35.3229; 14.5684
90; 95.522; 90		2682.24Sheppard, Daniel J.; Cameron, Scott A.; Tyler, Peter C.; Schwörer, Ralf
Comparison of disaccharide donors for heparan sulfate synthesis: uronic acids vs. their pyranose equivalents.
Organic & biomolecular chemistry, 2020, 18, 4728-4733
7157535 CIFC44 H46 Cl N3 O14P 21 21 218.1104; 19.5548; 27.2321
90; 90; 90		4318.9Sheppard, Daniel J.; Cameron, Scott A.; Tyler, Peter C.; Schwörer, Ralf
Comparison of disaccharide donors for heparan sulfate synthesis: uronic acids vs. their pyranose equivalents.
Organic & biomolecular chemistry, 2020, 18, 4728-4733
7157536 CIFC43 H45 N3 O14P 21 21 218.0833; 18.7876; 26.8116
90; 90; 90		4071.8Sheppard, Daniel J.; Cameron, Scott A.; Tyler, Peter C.; Schwörer, Ralf
Comparison of disaccharide donors for heparan sulfate synthesis: uronic acids vs. their pyranose equivalents.
Organic & biomolecular chemistry, 2020, 18, 4728-4733
7157537 CIFC33 H37 Cl3 N O2 PP -110.546; 12.611; 12.642
109.078; 94.549; 91.826		1581Jiang, Shuai-Shuai; Xiao, Yu-Ting; Wu, Yan-Chen; Luo, Shu-Zheng; Song, Ren-Jie; Li, Jin-Heng
Manganese(iii)-promoted tandem phosphinoylation/cyclization of 2-arylindoles/2-arylbenzimidazoles with disubstituted phosphine oxides.
Organic & biomolecular chemistry, 2020, 18, 4843-4847
7157538 CIFC25 H19 N3 O6P b c a15.1872; 16.3092; 34.3428
90; 90; 90		8506.4Panday, Anoop Kumar; Ali, Danish; Choudhury, Lokman H.
One-pot synthesis of pyrimidine linked naphthoquinone-fused pyrroles by iodine-mediated multicomponent reactions.
Organic & biomolecular chemistry, 2020, 18, 4997-5007
7157539 CIFC25 H16 F3 N3 O5P 1 21/c 112.391; 8.165; 21.573
90; 94.106; 90		2177Panday, Anoop Kumar; Ali, Danish; Choudhury, Lokman H.
One-pot synthesis of pyrimidine linked naphthoquinone-fused pyrroles by iodine-mediated multicomponent reactions.
Organic & biomolecular chemistry, 2020, 18, 4997-5007
7157540 CIFC30 H24 Cl3 N3 O6P -110.9534; 12.5947; 13.2276
100.624; 113.849; 110.012		1453.4Nguyen, Tuan K.; Titov, Gleb D.; Khoroshilova, Olesya V.; Kinzhalov, Mikhail A.; Rostovskii, Nikolai V.
Light-induced one-pot synthesis of pyrimidine derivatives from vinyl azides.
Organic & biomolecular chemistry, 2020, 18, 4971-4982
7157541 CIFC22 H22 N2 O6P 1 21/c 114.0485; 13.9573; 10.3547
90; 99.58; 90		2002.03Nguyen, Tuan K.; Titov, Gleb D.; Khoroshilova, Olesya V.; Kinzhalov, Mikhail A.; Rostovskii, Nikolai V.
Light-induced one-pot synthesis of pyrimidine derivatives from vinyl azides.
Organic & biomolecular chemistry, 2020, 18, 4971-4982
7157542 CIFC20 H14 Cl4 N2 O4P 1 21 110.8248; 16.4407; 12.0407
90; 109.771; 90		2016.53Nguyen, Tuan K.; Titov, Gleb D.; Khoroshilova, Olesya V.; Kinzhalov, Mikhail A.; Rostovskii, Nikolai V.
Light-induced one-pot synthesis of pyrimidine derivatives from vinyl azides.
Organic & biomolecular chemistry, 2020, 18, 4971-4982
7157543 CIFC90 H51 Cl3P 1 21/n 17.62; 43.657; 25.19
90; 90.53; 90		8380Yang, Yong; Nanjo, Yuki; Isobe, Hiroyuki; Sato, Sota
Synthesis and stereoisomerism of [n]cyclo-2,9-phenanthrenylene congeners possessing alternating E/Z- and R/S-biaryl linkages.
Organic & biomolecular chemistry, 2020, 18, 4949-4955
7157544 CIFC56 H32P 1 21/c 17.662; 15.949; 14.374
90; 99.232; 90		1733.8Yang, Yong; Nanjo, Yuki; Isobe, Hiroyuki; Sato, Sota
Synthesis and stereoisomerism of [n]cyclo-2,9-phenanthrenylene congeners possessing alternating E/Z- and R/S-biaryl linkages.
Organic & biomolecular chemistry, 2020, 18, 4949-4955
7157545 CIFC15 H10 Br I O2P -17.9349; 8.1555; 11.7247
108.099; 92.6644; 92.6		718.99Yang, Yong; Nanjo, Yuki; Isobe, Hiroyuki; Sato, Sota
Synthesis and stereoisomerism of [n]cyclo-2,9-phenanthrenylene congeners possessing alternating E/Z- and R/S-biaryl linkages.
Organic & biomolecular chemistry, 2020, 18, 4949-4955
7157546 CIFC20 H16 Cl N3 O2P 1 21/c 112.174; 12.709; 12.335
90; 117.06; 90		1699.5Tikhonova, Tatyana A.; Ilment, Nikita V.; Lyssenko, Konstantin A.; Zavarzin, Igor V.; Volkova, Yulia A.
Sulfur-mediated synthesis of unsymmetrically substituted N-aryl oxalamides by the cascade thioamidation/cyclocondensation and hydrolysis reaction.
Organic & biomolecular chemistry, 2020, 18, 5050-5060
7157547 CIFC22 H19 Cl N3 O3 SC 1 2/c 135.957; 6.1171; 19.5083
90; 96.604; 90		4262.4Tikhonova, Tatyana A.; Ilment, Nikita V.; Lyssenko, Konstantin A.; Zavarzin, Igor V.; Volkova, Yulia A.
Sulfur-mediated synthesis of unsymmetrically substituted N-aryl oxalamides by the cascade thioamidation/cyclocondensation and hydrolysis reaction.
Organic & biomolecular chemistry, 2020, 18, 5050-5060
7157548 CIFC18 H14 N4 OC 1 2/c 127.7141; 6.4562; 20.6251
90; 128.18; 90		2900.9Bou-Petit, Elisabeth; Plans, Arnau; Rodríguez-Picazo, Nieves; Torres-Coll, Antoni; Puigjaner, Cristina; Font-Bardia, Mercè; Teixidó, Jordi; Ramon Y Cajal, Santiago; Estrada-Tejedor, Roger; Borrell, José I
C4-C5 fused pyrazol-3-amines: when the degree of unsaturation and electronic characteristics of the fused ring controls regioselectivity in Ullmann and acylation reactions.
Organic & biomolecular chemistry, 2020, 18, 5145-5156
7157549 CIFC14 H16 N4 O3P 1 21/c 110.0257; 13.4533; 10.8045
90; 108.456; 90		1382.34Bou-Petit, Elisabeth; Plans, Arnau; Rodríguez-Picazo, Nieves; Torres-Coll, Antoni; Puigjaner, Cristina; Font-Bardia, Mercè; Teixidó, Jordi; Ramon Y Cajal, Santiago; Estrada-Tejedor, Roger; Borrell, José I
C4-C5 fused pyrazol-3-amines: when the degree of unsaturation and electronic characteristics of the fused ring controls regioselectivity in Ullmann and acylation reactions.
Organic & biomolecular chemistry, 2020, 18, 5145-5156
7157550 CIFC16 H17 NP 21 21 217.2231; 14.5123; 22.3944
90; 90; 90		2347.47Zonker, Benjamin; Duman, Ediz; Hausmann, Heike; Becker, Jonathan; Hrdina, Radim
[1,2]-Rearrangement of iminium salts provides access to heterocycles with adamantane scaffold.
Organic & biomolecular chemistry, 2020, 18, 4941-4945
7157551 CIFC20 H26 N OC 1 2/c 127.1498; 10.3031; 11.3085
90; 91.1403; 90		3162.67Zonker, Benjamin; Duman, Ediz; Hausmann, Heike; Becker, Jonathan; Hrdina, Radim
[1,2]-Rearrangement of iminium salts provides access to heterocycles with adamantane scaffold.
Organic & biomolecular chemistry, 2020, 18, 4941-4945
7157552 CIFC55 H33 Cl3 F15 N5 OP -113.2433; 13.7134; 15.7312
70.848; 80.596; 66.09		2465.69Mori, Daiki; Yoneda, Tomoki; Suzuki, Masaaki; Hoshino, Tyuji; Neya, Saburo
Deprotection of a benzyl unit induces a 22π aromatic macrocycle of 3-oxypyripentaphyrin(0.1.1.1.0) with strong NIR absorption.
Organic & biomolecular chemistry, 2020, 18, 5334-5338
7157553 CIFC48 H24 Cl6 F15 N5 OP -112.2776; 13.0559; 16.5083
105.241; 110.613; 98.939		2297.85Mori, Daiki; Yoneda, Tomoki; Suzuki, Masaaki; Hoshino, Tyuji; Neya, Saburo
Deprotection of a benzyl unit induces a 22π aromatic macrocycle of 3-oxypyripentaphyrin(0.1.1.1.0) with strong NIR absorption.
Organic & biomolecular chemistry, 2020, 18, 5334-5338
7157554 CIFC29 H35 N3 O6P 1 21 17.9726; 30.0112; 11.2602
90; 100.176; 90		2651.82Young, Matthew J.; Akien, Geoffrey R.; Evans, Nicholas H.
An amide hydrogen bond templated [1]rotaxane displaying a peptide motif - demonstrating an expedient route to synthetic mimics of lasso peptides.
Organic & biomolecular chemistry, 2020, 18, 5203-5209
7157555 CIFC38 H40 Br N O2P 21 21 2110.382; 15.766; 20.036
90; 90; 90		3279.5Wu, Shu-Fang; Tu, Man-Su; Hang, Qing-Qing; Zhang, Shu; Ding, Haixia; Zhang, Yu-Chen; Shi, Feng
Construction of chiral chroman scaffolds via catalytic asymmetric (4 + 2) cyclizations of para-quinone methide derivatives with 3-vinylindoles.
Organic & biomolecular chemistry, 2020, 18, 5388-5399
7157556 CIFC28.75 H27 Br N2 O4C 1 2 125.7843; 5.307; 18.5521
90; 95.228; 90		2528.06Roesner, Stefan; Beadle, Jonathan D.; Tam, Leo K. B.; Wilkening, Ina; Clarkson, Guy J.; Raubo, Piotr; Shipman, Michael
Development of oxetane modified building blocks for peptide synthesis.
Organic & biomolecular chemistry, 2020, 18, 5400-5405
7157557 CIFC22 H18 O2P 1 21/n 111.536; 8.2902; 18.32
90; 108.28; 90		1663.6Zhang, Heng; Yu, Yinghua; Huang, Xueliang
Facile access to 2,2-diaryl 2H-chromenes through a palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones.
Organic & biomolecular chemistry, 2020, 18, 5115-5119
7157558 CIFC21 H16.5 Br2 O2.25P 4/n :220.474; 20.474; 9.72
90; 90; 90		4074.5Zhang, Heng; Yu, Yinghua; Huang, Xueliang
Facile access to 2,2-diaryl 2H-chromenes through a palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones.
Organic & biomolecular chemistry, 2020, 18, 5115-5119
7157559 CIFC28 H24 O2 SP -19.99; 10.558; 21.868
78.978; 77.06; 85.471		2204.9Zhang, Heng; Yu, Yinghua; Huang, Xueliang
Facile access to 2,2-diaryl 2H-chromenes through a palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones.
Organic & biomolecular chemistry, 2020, 18, 5115-5119
7157560 CIFC25 H17 Br OP 1 21/c 116.94; 10.721; 10.61
90; 101.81; 90		1886.1Zhang, Heng; Yu, Yinghua; Huang, Xueliang
Facile access to 2,2-diaryl 2H-chromenes through a palladium-catalyzed cascade reaction of ortho-vinyl bromobenzenes with N-tosylhydrazones.
Organic & biomolecular chemistry, 2020, 18, 5115-5119
7157561 CIFC33 H32 F2 O2P n a 2119.4194; 6.3668; 42.5242
90; 90; 90		5257.7Kim, Jung Keun; Gong, Ming; Shokova, Elvira A.; Tafeenko, Viktor A.; Kovaleva, Olga V.; Wu, Yangjie; Kovalev, Vladimir V.
Pyrazoles: 'one-pot' synthesis from arenes and carboxylic acids.
Organic & biomolecular chemistry, 2020, 18, 5625-5638
7157562 CIFC27 H26 F2 N2P 1 21/n 115.0563; 9.004; 17.4709
90; 100.4; 90		2329.57Kim, Jung Keun; Gong, Ming; Shokova, Elvira A.; Tafeenko, Viktor A.; Kovaleva, Olga V.; Wu, Yangjie; Kovalev, Vladimir V.
Pyrazoles: 'one-pot' synthesis from arenes and carboxylic acids.
Organic & biomolecular chemistry, 2020, 18, 5625-5638
7157563 CIFC70 H74 Cl4 F4 N4 O5P -113.0983; 14.8761; 16.8995
89.435; 81.488; 87.41		3253.28Kim, Jung Keun; Gong, Ming; Shokova, Elvira A.; Tafeenko, Viktor A.; Kovaleva, Olga V.; Wu, Yangjie; Kovalev, Vladimir V.
Pyrazoles: 'one-pot' synthesis from arenes and carboxylic acids.
Organic & biomolecular chemistry, 2020, 18, 5625-5638
7157564 CIFC46 H45 N6 O7 S2P 21 21 2110.295; 11.374; 36.37
90; 90; 90		4259Salunke, Rahul Vilas; Mishra, Pawan Kumar; Sanghvi, Yogesh S.; Ramesh, Namakkal G.
Synthesis of novel homoazanucleosides and their peptidyl analogs.
Organic & biomolecular chemistry, 2020, 18, 5639-5651
7157565 CIFC11 H20 Cl2 N4 O4P 21 21 215.4636; 15.231; 18.032
90; 90; 90		1500.6Salunke, Rahul Vilas; Mishra, Pawan Kumar; Sanghvi, Yogesh S.; Ramesh, Namakkal G.
Synthesis of novel homoazanucleosides and their peptidyl analogs.
Organic & biomolecular chemistry, 2020, 18, 5639-5651
7157566 CIFC44 H46 Cl Fe2 N2 O2 P Pd2P 21 21 2112.1801; 12.77485; 25.8213
90; 90; 90		4017.77Arthurs, Ross A.; Hughes, David L.; Richards, Christopher J.
Planar chiral palladacycle precatalysts for asymmetric synthesis.
Organic & biomolecular chemistry, 2020, 18, 5466-5472
7157567 CIFC25 H19 F N2 O2P 1 21 16.155; 15.283; 10.6069
90; 94.491; 90		994.69Saini, Kapil Mohan; Saunthwal, Rakesh K.; Sushmita, ?; Verma, Akhilesh K.
Synthesis of cyclopentaquinolinone and cyclopentapyridinone from ortho-alkynyl-N-arylaldehyde via superbase-promoted C-N, C-O and C-C bond formation.
Organic & biomolecular chemistry, 2020, 18, 5594-5601
7157568 CIFC31 H21 F3 N6 OP 1 21/c 116.8293; 16.2265; 20.227
90; 109.526; 90		5205.93Deng, Jiajie; Wu, Xueting; Guo, Guiling; Zhao, Xiaohu; Yu, Zhipeng
Photoisomerization-enhanced 1,3-dipolar cycloaddition of carbon-bridged octocyclic azobenzene with photo-released nitrile imine for peptide stapling and imaging in live cells.
Organic & biomolecular chemistry, 2020, 18, 5602-5607
7157569 CIFC14 H12 N2P b c a12.3316; 12.7106; 14.1603
90; 90; 90		2219.51Deng, Jiajie; Wu, Xueting; Guo, Guiling; Zhao, Xiaohu; Yu, Zhipeng
Photoisomerization-enhanced 1,3-dipolar cycloaddition of carbon-bridged octocyclic azobenzene with photo-released nitrile imine for peptide stapling and imaging in live cells.
Organic & biomolecular chemistry, 2020, 18, 5602-5607
7157570 CIFC18 H22 N2 O4 SP 1 21 14.7274; 17.782; 10.734
90; 98.994; 90		891.23Zhao, Jia-Hui; Zhou, Zhao-Zhao; Zhang, Yue; Su, Xuan; Chen, Xi-Meng; Liang, Yong-Min
Visible-light-mediated borylation of aryl and alkyl halides with a palladium complex.
Organic & biomolecular chemistry, 2020, 18, 4390-4394
7157571 CIFC23 H21 Br OP 1 21/n 15.6626; 9.7839; 32.396
90; 89.786; 90		1794.8Satam, Nishikant; Nemu, Saumyadip; Gururaja, Guddeangadi N.; Namboothiri, Irishi N. N.
Substrate-oriented selectivity in the Mg-mediated conjugate addition of bromoform to electron-deficient alkenes.
Organic & biomolecular chemistry, 2020, 18, 5697-5707
7157572 CIFC22 H20 Br2 OP 1 21/c 19.3505; 14.6227; 13.7913
90; 94.177; 90		1880.67Satam, Nishikant; Nemu, Saumyadip; Gururaja, Guddeangadi N.; Namboothiri, Irishi N. N.
Substrate-oriented selectivity in the Mg-mediated conjugate addition of bromoform to electron-deficient alkenes.
Organic & biomolecular chemistry, 2020, 18, 5697-5707
7157573 CIFC23 H17 Br2 N OP 1 21/c 19.541; 16.928; 12.1
90; 102.664; 90		1906.7Satam, Nishikant; Nemu, Saumyadip; Gururaja, Guddeangadi N.; Namboothiri, Irishi N. N.
Substrate-oriented selectivity in the Mg-mediated conjugate addition of bromoform to electron-deficient alkenes.
Organic & biomolecular chemistry, 2020, 18, 5697-5707
7157574 CIFC27 H24 N4 O5P -18.002; 12.123; 12.728
75.11; 76.29; 77.95		1144.8Cheng, Cheng; Sun, Xiaobin; Miao, Zhiwei
A PPh<sub>3</sub>-catalyzed sequential annulation reaction to construct cyclopentane-fused dihydropyrazolone-pyrrolidinediones.
Organic & biomolecular chemistry, 2020, 18, 5577-5581
7157575 CIFC33 H35 F O3P 1 21 19.2914; 14.7113; 9.9029
90; 94.55; 90		1349.35Przydacz, Artur; Dyguda, Mateusz; Topolska, Aleksandra; Skrzyńska, Anna; Xu, Chang-Jiang; Chen, Ying-Chun; Albrecht, Łukasz
Doubly vinylogous and doubly rearomative functionalization of 2-alkyl-3-furfurals.
Organic & biomolecular chemistry, 2020, 18, 5816-5821
7157576 CIFC58 H60 O8P 1 21/n 112.1334; 10.35; 18.7632
90; 95.327; 90		2346.1Basu, Pallabita; Satam, Nishikant; Namboothiri, Irishi N. N.
Synthesis of indenofurans, benzofurans and spiro-lactones via Hauser-Kraus annulation involving 1,6-addition of phthalide to quinone methides.
Organic & biomolecular chemistry, 2020, 18, 5677-5687
7157577 CIFC29 H30 O4P b c a19.904; 11.4024; 21.6619
90; 90; 90		4916.2Basu, Pallabita; Satam, Nishikant; Namboothiri, Irishi N. N.
Synthesis of indenofurans, benzofurans and spiro-lactones via Hauser-Kraus annulation involving 1,6-addition of phthalide to quinone methides.
Organic & biomolecular chemistry, 2020, 18, 5677-5687
7157578 CIFC30 H30 O4P 1 21/n 18.648; 17.1737; 18.084
90; 98.244; 90		2658Basu, Pallabita; Satam, Nishikant; Namboothiri, Irishi N. N.
Synthesis of indenofurans, benzofurans and spiro-lactones via Hauser-Kraus annulation involving 1,6-addition of phthalide to quinone methides.
Organic & biomolecular chemistry, 2020, 18, 5677-5687
7157579 CIFC26 H15 ClP 1 21/n 18.1345; 11.3251; 19.1576
90; 92.945; 90		1762.54Takano, Hideaki; Okazaki, Sari; Nishibe, Shun; Ito, Takeharu; Shiozawa, Natsumi; Sugimura, Natsuhiko; Kanyiva, Kyalo Stephen; Shibata, Takanori
Gold-catalyzed dual C-C bond cleavage of biphenylenes bearing a pendant alkyne at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 5826-5831
7157580 CIFC23 H17 ClP -17.5655; 10.9027; 11.088
113.594; 103.447; 93.898		801.74Takano, Hideaki; Okazaki, Sari; Nishibe, Shun; Ito, Takeharu; Shiozawa, Natsumi; Sugimura, Natsuhiko; Kanyiva, Kyalo Stephen; Shibata, Takanori
Gold-catalyzed dual C-C bond cleavage of biphenylenes bearing a pendant alkyne at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 5826-5831
7157581 CIFC23 H17 ClC 1 2/c 119.2706; 4.9741; 33.688
90; 102.847; 90		3148.3Takano, Hideaki; Okazaki, Sari; Nishibe, Shun; Ito, Takeharu; Shiozawa, Natsumi; Sugimura, Natsuhiko; Kanyiva, Kyalo Stephen; Shibata, Takanori
Gold-catalyzed dual C-C bond cleavage of biphenylenes bearing a pendant alkyne at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 5826-5831
7157582 CIFC29 H20 F3 N O2P -110.333; 10.46; 11.583
88.838; 68.455; 79.684		1144.2Zhang, Yi-Zhu; Sheng, Feng-Tao; Zhu, Zuoquan; Li, Zhi-Ming; Zhang, Shu; Tan, Wei; Shi, Feng
Organocatalytic C3-functionalization of indolizines: synthesis of biologically important indolizine derivatives.
Organic & biomolecular chemistry, 2020, 18, 5688-5696
7157583 CIFC10 H9 F3 O3 SP 1 21/c 14.837; 12.644; 18.82
90; 91.7; 90		1150.5Wang, Meng-Yue; Zhu, Xue-Qing; Zhang, Xing-Long; Guo, Rui-Li; Jia, Qiong; Wang, Yong-Qiang
Synthesis of trifluoromethylthioesters from aldehydes via a visible light-promoted radical process.
Organic & biomolecular chemistry, 2020, 18, 5918-5926
7157584 CIFC33 H36 O5P c c n23.1727; 29.8856; 8.3703
90; 90; 90		5796.7Weber, Carina; Vierengel, Nina; Walter, Thorsten; Behrendt, Torsten; Lucas, Tobias; Erkel, Gerhard; Opatz, Till
Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones.
Organic & biomolecular chemistry, 2020, 18, 5906-5917
7157585 CIFC34 H38 O5P 1 21/n 17.2297; 15.8502; 25.683
90; 95.935; 90		2927.3Weber, Carina; Vierengel, Nina; Walter, Thorsten; Behrendt, Torsten; Lucas, Tobias; Erkel, Gerhard; Opatz, Till
Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones.
Organic & biomolecular chemistry, 2020, 18, 5906-5917
7157586 CIFC19 H23 Cl O5I b a 211.1913; 36.617; 8.3725
90; 90; 90		3431Weber, Carina; Vierengel, Nina; Walter, Thorsten; Behrendt, Torsten; Lucas, Tobias; Erkel, Gerhard; Opatz, Till
Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones.
Organic & biomolecular chemistry, 2020, 18, 5906-5917
7157587 CIFC11 H12 O3P 1 21/n 17.5792; 17.262; 7.5865
90; 95.065; 90		988.68Ren, Panlong; Miao, Xinyu; Tang, Ting; Wu, Yueting; Wang, Jing; Zeng, Ying; Li, Yun; Gao, Kun; Yang, Yan-Long
Construction of a meroterpenoid-like compound collection by precursor-assisted biosynthesis.
Organic & biomolecular chemistry, 2020, 18, 5850-5856
7157588 CIFC16 H22 O5P c c a32.6901; 12.36143; 7.35394
90; 90; 90		2971.7Ren, Panlong; Miao, Xinyu; Tang, Ting; Wu, Yueting; Wang, Jing; Zeng, Ying; Li, Yun; Gao, Kun; Yang, Yan-Long
Construction of a meroterpenoid-like compound collection by precursor-assisted biosynthesis.
Organic & biomolecular chemistry, 2020, 18, 5850-5856
7157589 CIFC19 H26 O4P 1 21/n 110.2175; 13.7827; 12.933
90; 111.529; 90		1694.22Ren, Panlong; Miao, Xinyu; Tang, Ting; Wu, Yueting; Wang, Jing; Zeng, Ying; Li, Yun; Gao, Kun; Yang, Yan-Long
Construction of a meroterpenoid-like compound collection by precursor-assisted biosynthesis.
Organic & biomolecular chemistry, 2020, 18, 5850-5856
7157590 CIFC16 H22 O4P 21 21 218.3946; 11.481; 15.2872
90; 90; 90		1473.36Ren, Panlong; Miao, Xinyu; Tang, Ting; Wu, Yueting; Wang, Jing; Zeng, Ying; Li, Yun; Gao, Kun; Yang, Yan-Long
Construction of a meroterpenoid-like compound collection by precursor-assisted biosynthesis.
Organic & biomolecular chemistry, 2020, 18, 5850-5856
7157591 CIFC17 H24 O4C 1 2/c 127.5479; 6.3331; 18.4336
90; 91.28; 90		3215.19Ren, Panlong; Miao, Xinyu; Tang, Ting; Wu, Yueting; Wang, Jing; Zeng, Ying; Li, Yun; Gao, Kun; Yang, Yan-Long
Construction of a meroterpenoid-like compound collection by precursor-assisted biosynthesis.
Organic & biomolecular chemistry, 2020, 18, 5850-5856
7157592 CIFC38 H29 N O3P -19.8324; 10.2354; 15.6234
103.229; 97.742; 105.191		1445.05Yang, Ye-Fei; Huang, Xiao-Bo; Gao, Wen-Xia; Zhou, Yun-Bing; Liu, Miao-Chang; Wu, Hua-Yue
Ag<sub>2</sub>O-promoted ring-opening reactions of cyclopropenones with oximes.
Organic & biomolecular chemistry, 2020, 18, 5822-5825
7157593 CIFC15 H14 N2 O S2P 1 21/n 19.0969; 11.7978; 14.1107
90; 97.79; 90		1500.4Shally, ?; Althagafi, Ismail; Shaw, Ranjay; Elagamy, Amr; Kumar, Abhinav; Pratap, Ramendra
A [5 + 1] annulation strategy for the synthesis of multifunctional biaryls and p-teraryls from 1,6-Michael acceptor ketene dithioacetals.
Organic & biomolecular chemistry, 2020, 18, 6407-6417
7157594 CIFC20 H14 Br N3 O2 SP -18.4509; 10.7362; 11.5735
108.414; 104.992; 100.036		924.09Shally, ?; Althagafi, Ismail; Shaw, Ranjay; Elagamy, Amr; Kumar, Abhinav; Pratap, Ramendra
A [5 + 1] annulation strategy for the synthesis of multifunctional biaryls and p-teraryls from 1,6-Michael acceptor ketene dithioacetals.
Organic & biomolecular chemistry, 2020, 18, 6407-6417
7157595 CIFC23 H26 N2P -18.2991; 9.0692; 13.6609
94.077; 104.535; 105.981		945.91Shaw, Ranjay; Althagafi, Ismail; Elagamy, Amr; Rai, Reeta; Shah, Chandan; Nemaysh, Vishal; Singh, Harpreet; Pratap, Ramendra
Transition metal-free synthesis of sterically hindered allylarenes from 5-hexene-2-one.
Organic & biomolecular chemistry, 2020, 18, 6276-6286
7157596 CIFC2.483 H2.345 N0.138 S0.138P 1 21/c 19.0216; 10.1719; 17.318
90; 101.519; 90		1557.21Shaw, Ranjay; Althagafi, Ismail; Elagamy, Amr; Rai, Reeta; Shah, Chandan; Nemaysh, Vishal; Singh, Harpreet; Pratap, Ramendra
Transition metal-free synthesis of sterically hindered allylarenes from 5-hexene-2-one.
Organic & biomolecular chemistry, 2020, 18, 6276-6286
7157597 CIFC17 H13 N O2 SP b c a7.6988; 11.4847; 30.9861
90; 90; 90		2739.74Dai, Tianzi; Cui, Chen; Qi, Xueyu; Cheng, Yanshu; He, Qian; Zhang, Xiaofei; Luo, Xiaomin; Yang, Chunhao
Regioselective synthesis of substituted thiazoles via cascade reactions from 3-chlorochromones and thioamides.
Organic & biomolecular chemistry, 2020, 18, 6162-6170
7157598 CIFC20 H15 N O2 SP 1 21/c 17.4364; 26.4068; 8.4485
90; 94.973; 90		1652.8Sarkar, Writhabrata; Bhowmik, Arup; Das, Sumit; Sulekha, Aiswarya Balaram; Mishra, Aniket; Deb, Indubhusan
Iridium-catalyzed direct C-H arylation of cyclic <i>N</i>-sulfonyl ketimines with arylsiloxanes at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 7074-7078
7157599 CIFC19 H13 N O3 SP 1 21/n 19.9907; 8.1808; 19.0908
90; 90.216; 90		1560.32Sarkar, Writhabrata; Bhowmik, Arup; Das, Sumit; Sulekha, Aiswarya Balaram; Mishra, Aniket; Deb, Indubhusan
Iridium-catalyzed direct C-H arylation of cyclic <i>N</i>-sulfonyl ketimines with arylsiloxanes at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 7074-7078
7157600 CIFC20 H15 N O4 SP 1 21/n 18.107; 11.495; 19.194
90; 93.585; 90		1785Sarkar, Writhabrata; Bhowmik, Arup; Das, Sumit; Sulekha, Aiswarya Balaram; Mishra, Aniket; Deb, Indubhusan
Iridium-catalyzed direct C-H arylation of cyclic <i>N</i>-sulfonyl ketimines with arylsiloxanes at ambient temperature.
Organic & biomolecular chemistry, 2020, 18, 7074-7078
7157601 CIFC16 H17 N O6P 1 21/c 119.975; 4.999; 17.26
90; 110.614; 90		1613.1Cheng, Bin; Li, Hui; Duan, Shengguo; Zhang, Xinping; He, Yixuan; Li, Yuntong; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of indolizines from pyridinium 1,4-zwitterionic thiolates and propiolic acid derivatives via a formal [4 + 1] pathway.
Organic & biomolecular chemistry, 2020, 18, 6253-6257
7157602 CIFC34 H32 N4 O2P 1 21/c 112.4739; 7.4371; 16.2909
90; 110.59; 90		1414.8Aegurla, Balakrishna; Jarwal, Nisha; Peddinti, Rama Krishna
Denitrative imino-diaza-Nazarov cyclization: synthesis of pyrazoles.
Organic & biomolecular chemistry, 2020, 18, 6100-6107
7157603 CIFC16 H18 B F4 I O2P -17.4922; 10.184; 11.624
87.81; 75.567; 79.756		845.2Abudken, Ahmed M. H.; Hope, Eric G.; Singh, Kuldip; Stuart, Alison M.
Fluorinations of unsymmetrical diaryliodonium salts containing ortho-sidearms; influence of sidearm on selectivity.
Organic & biomolecular chemistry, 2020, 18, 6140-6146
7157604 CIFC21 H20 B F4 I O2P 1 21/n 112.965; 11.911; 13.389
90; 102.163; 90		2021.2Abudken, Ahmed M. H.; Hope, Eric G.; Singh, Kuldip; Stuart, Alison M.
Fluorinations of unsymmetrical diaryliodonium salts containing ortho-sidearms; influence of sidearm on selectivity.
Organic & biomolecular chemistry, 2020, 18, 6140-6146
7157605 CIFC21 H18 B F4 I OP b c a11.995; 14.196; 22.602
90; 90; 90		3849Abudken, Ahmed M. H.; Hope, Eric G.; Singh, Kuldip; Stuart, Alison M.
Fluorinations of unsymmetrical diaryliodonium salts containing ortho-sidearms; influence of sidearm on selectivity.
Organic & biomolecular chemistry, 2020, 18, 6140-6146
7157606 CIFC22 H18 F3 I O4 SP -18.4537; 11.6591; 12.124
66.609; 87.336; 76.601		1065.5Abudken, Ahmed M. H.; Hope, Eric G.; Singh, Kuldip; Stuart, Alison M.
Fluorinations of unsymmetrical diaryliodonium salts containing ortho-sidearms; influence of sidearm on selectivity.
Organic & biomolecular chemistry, 2020, 18, 6140-6146
7157607 CIFC28 H25 I O4 SP -113.148; 13.175; 16.115
83.966; 86.472; 60.099		2406.4Abudken, Ahmed M. H.; Hope, Eric G.; Singh, Kuldip; Stuart, Alison M.
Fluorinations of unsymmetrical diaryliodonium salts containing ortho-sidearms; influence of sidearm on selectivity.
Organic & biomolecular chemistry, 2020, 18, 6140-6146
7157608 CIFC90 H117 N3 O18 S3P -115.542; 16.5195; 20.2175
74.481; 69.188; 67.602		4433.3Cera, Gianpiero; Balestri, Davide; Bazzoni, Margherita; Marchiò, Luciano; Secchi, Andrea; Arduini, Arturo
Trisulfonamide calix[6]arene-catalysed Michael addition to nitroalkenes.
Organic & biomolecular chemistry, 2020, 18, 6241-6246
7157609 CIFC128 H72 N16 O16P 1 21/n 115.8835; 7.9818; 18.7804
90; 98.45; 90		2355.11Hong, Hyejin; Conover, Cassidy M.; Hofsommer, Dillon T.; Sanz, Corey A.; Hicks, Robin G.
Discovery and properties of a new indigoid structure type based on dimeric cis-indigos.
Organic & biomolecular chemistry, 2020, 18, 5838-5842
7157610 CIFC28 H17.07 N2.13 O3.2C 1 2/c 139.337; 13.8936; 28.683
90; 93.498; 90		15647Hong, Hyejin; Conover, Cassidy M.; Hofsommer, Dillon T.; Sanz, Corey A.; Hicks, Robin G.
Discovery and properties of a new indigoid structure type based on dimeric cis-indigos.
Organic & biomolecular chemistry, 2020, 18, 5838-5842
7157611 CIFC256 H152 N32 O36C 1 2/c 127.7629; 10.8917; 17.5795
90; 113.574; 90		4872.1Hong, Hyejin; Conover, Cassidy M.; Hofsommer, Dillon T.; Sanz, Corey A.; Hicks, Robin G.
Discovery and properties of a new indigoid structure type based on dimeric cis-indigos.
Organic & biomolecular chemistry, 2020, 18, 5838-5842
7157612 CIFC21 H16 Br N O4 SP 1 21/c 18.2647; 19.7204; 11.6058
90; 95.308; 90		1883.44Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157613 CIFC31 H23 N2 O5P 1 21/n 111.8834; 8.8469; 23.6723
90; 91.109; 90		2488.2Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157614 CIFC33 H27 Br2 N2 O5P 1 21/c 113.1453; 12.9849; 16.874
90; 96.328; 90		2862.7Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157615 CIFC39 H28 N2 O5P -113.89; 16.8786; 17.2527
64.295; 88.306; 73.213		3467.7Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157616 CIFC66 H56 Br4 N4 O12P -113.3171; 15.1045; 16.7543
77.235; 76.167; 67.821		2998Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157617 CIFC33 H24 Br2 Cl3 N2 O5P 1 21/c 110.533; 26.861; 12.2233
90; 115.334; 90		3125.7Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157618 CIFC31 H22 Cl2 N2 O5P -110.9174; 11.9111; 12.3891
69.112; 87.877; 65.53		1358.3Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157619 CIFC31 H22 Cl2 N2 O5P -110.8001; 11.3693; 13.4193
89.11; 67.91; 68.542		1406.67Chang, Meng-Yang; Chen, Kuan-Ting; Chen, Han-Yu
One-pot construction of dispirocyclohexanes via K<sub>2</sub>CO<sub>3</sub>-mediated desulfonylative Michael-Michael-aldol (2 + 2 + 2) annulation of sulfonyl 2-pyridyl flavanones and methylketones.
Organic & biomolecular chemistry, 2020, 18, 6297-6311
7157620 CIFC20 H27 N7 O12P 21 21 219.29096; 14.5006; 20.3184
90; 90; 90		2737.39He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157621 CIFC40 H35 N7 O12P 31 2 119.7672; 19.7672; 23.6968
90; 90; 120		8018.8He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157622 CIFC14 H16 Cl3 N6 O8P 21 21 218.6304; 10.8741; 22.9325
90; 90; 90		2152.2He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157623 CIFC18 H24 N10 O10P 21 21 218.6075; 10.7485; 33.736
90; 90; 90		3121.2He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157624 CIFC13 H16 N6 O8P 21 21 217.2784; 9.2019; 26.166
90; 90; 90		1752.5He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157625 CIFC17 H22 N6 O11P 1 21 19.2129; 40.7685; 12.8563
90; 90.32; 90		4828.7He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157626 CIFC37 H39 F3 N8 O13P 1 21 112.9906; 11.1438; 14.8377
90; 103.257; 90		2090.73He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157627 CIFC17 H22 N6 O11P 1 21 17.7778; 13.2995; 11.4128
90; 91.458; 90		1180.17He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157628 CIFC20 H27 N7 O12P 1 21 19.6273; 8.8714; 16.549
90; 101.469; 90		1385.2He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157629 CIFC11 H11 N O2P 21 21 217.5291; 7.4902; 17.0281
90; 90; 90		960.29Braire, Julien; Dorcet, Vincent; Vidal, Joëlle; Lalli, Claudia; Carreaux, François
BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine.
Organic & biomolecular chemistry, 2020, 18, 6042-6046
7157630 CIFC12 H13 N O2P 21 21 217.3607; 8.0406; 17.598
90; 90; 90		1041.5Braire, Julien; Dorcet, Vincent; Vidal, Joëlle; Lalli, Claudia; Carreaux, François
BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine.
Organic & biomolecular chemistry, 2020, 18, 6042-6046
7157631 CIFC24 H17.19 N3 O1.1P 1 21/n 110.5627; 8.8564; 19.8868
90; 98.7088; 90		1838.91Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157632 CIFC15 H14 N2 O2P 1 21/c 119.1254; 5.4936; 11.5714
90; 98.8783; 90		1201.21Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157633 CIFC24.25 H14.5 Br3 Cl0.5 N3 OC 1 2/c 126.7209; 15.6427; 11.8698
90; 104.361; 90		4806.38Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157634 CIFC27 H23 N3 OP -110.4157; 10.5063; 11.3815
112.529; 108.753; 99.9684		1024.96Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157635 CIFC9 H9 N O2P 1 n 114.1319; 3.8682; 15.5153
90; 110.946; 90		792.1Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157636 CIFC17 H28 O4P 1 21/c 115.2304; 9.1246; 22.238
90; 95.627; 90		3075.6Kobayashi, Toyoharu; Tomita, Yui; Kawamoto, Yuichiro; Ito, Hisanaka
Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol.
Organic & biomolecular chemistry, 2020, 18, 7316-7320
7157637 CIFC20 H32 O4P 1 21/c 110.559; 8.9149; 19.341
90; 92.146; 90		1819.3Kobayashi, Toyoharu; Tomita, Yui; Kawamoto, Yuichiro; Ito, Hisanaka
Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol.
Organic & biomolecular chemistry, 2020, 18, 7316-7320
7157638 CIFC28 H30 N2 O3 S4P 21 21 219.4421; 14.8451; 19.2118
90; 90; 90		2692.9García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157639 CIFC22 H18 N2 O3 S4R -3 :H23.7837; 23.7837; 21.6038
90; 90; 120		10583.3García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157640 CIFC34 H26 N2 O3 S4P 21 21 2112.482; 12.8583; 19.5132
90; 90; 90		3131.82García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157641 CIFC16 H12 Br N3P 1 21/n 17.1264; 19.867; 19.419
90; 94.326; 90		2741.5Chatterjee, Arpita; Murmu, Chudamani; Peruncheralathan, S.
Copper-catalysed <i>N</i>-arylation of 5-aminopyrazoles: a simple route to pyrazolo[3,4-<i>b</i>]indoles.
Organic & biomolecular chemistry, 2020, 18, 6571-6581
7157642 CIFC36.5 H28 Cl2 O4F d d 259.6625; 17.3644; 11.0242
90; 90; 90		11421.1Tanaka, Kenta; Asada, Yosuke; Hoshino, Yujiro; Honda, Kiyoshi
Visible-light-induced [4 + 2] cycloaddition of pentafulvenes by organic photoredox catalysis.
Organic & biomolecular chemistry, 2020, 18, 8074-8078
7157643 CIFC33 H24 Cl2 O4P 1 21/c 115.2283; 9.8746; 18.4264
90; 110.126; 90		2601.65Tanaka, Kenta; Asada, Yosuke; Hoshino, Yujiro; Honda, Kiyoshi
Visible-light-induced [4 + 2] cycloaddition of pentafulvenes by organic photoredox catalysis.
Organic & biomolecular chemistry, 2020, 18, 8074-8078
7157644 CIFC21 H16 N2 O4P b c n17.6367; 13.5661; 14.5573
90; 90; 90		3483Sharma, Suraj; Dutta, Nibedita Baruah; Bhuyan, Mayurakhi; Das, Babulal; Baishya, Gakul
<i>tert</i>-Butylhydroperoxide (TBHP) mediated oxidative cross-dehydrogenative coupling of quinoxalin-2(1<i>H</i>)-ones with 4-hydroxycoumarins, 4-hydroxy-6-methyl-2-pyrone and 2-hydroxy-1,4-naphthoquinone under metal-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6537-6548
7157645 CIFC24 H32 N4 O8P c a 219.621; 8.003; 33.196
90; 90; 90		2556Taily, Irshad Maajid; Saha, Debarshi; Banerjee, Prabal
Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones.
Organic & biomolecular chemistry, 2020, 18, 6564-6570
7157646 CIFC26 H27 Br N2 O5P 1 21/c 18.0617; 26.398; 11.8969
90; 91.684; 90		2530.7Taily, Irshad Maajid; Saha, Debarshi; Banerjee, Prabal
Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones.
Organic & biomolecular chemistry, 2020, 18, 6564-6570
7157647 CIFC19 H17 Br N2 O2P 1 21/c 110.495; 21.897; 7.842
90; 96.57; 90		1790.3Ma, Liyao; Ou, Pengcheng; Huang, Xueliang
Divergent synthesis of 1,3,5-tri and 1,3-disubstituted pyrazoles under transition metal-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6487-6491
7157648 CIFC20 H15 N O3P b c a13.5094; 11.092; 21.2668
90; 90; 90		3186.8Yang, Fazhou; Liu, Ziyan; Liu, Hao; Shangguan, Yu; Deng, Hao; Huang, Jiaxing; Xiao, Yumei; Guo, Hongchao; Zhang, Cheng
Cu-Catalysed synthesis of benzo[f]indole-2,4,9(3H)-triones by the reaction of 2-amino-1,4-napthoquinones with α-bromocarboxylates.
Organic & biomolecular chemistry, 2020, 18, 6724-6731
7157649 CIFC19 H23 Cl2 N3 O4 S2P n m a15.0501; 23.9887; 6.1915
90; 90; 90		2235.33Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157650 CIFC19 H23 F2 N3 O4 S2P 1 21/c 115.0587; 11.9394; 11.6556
90; 90.844; 90		2095.4Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157651 CIFC20 H23 Cl5 D N3 O4 S2P 21 21 2110.5857; 14.0014; 17.5197
90; 90; 90		2596.68Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157652 CIFC19 H23 Cl2 N3 O4 S2P n m a15.0515; 23.4696; 6.1833
90; 90; 90		2184.27Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157653 CIFC19 H23 Br2 N3 O4 S2P n m a15.1555; 24.3132; 6.1544
90; 90; 90		2267.77Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157654 CIFC20 H23 Cl3 D F2 N3 O4 S2P 21 21 2110.4481; 14.3121; 16.4591
90; 90; 90		2461.2Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157655 CIFC19 H23 I2 N3 O4 S2P n m a15.4374; 24.9622; 6.1336
90; 90; 90		2363.59Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157656 CIFC19 H23 I2 N3 O4 S2P n m a15.4193; 24.5788; 6.1039
90; 90; 90		2313.3Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157657 CIFC28 H32 O8I -431.5358; 31.5358; 5.2684
90; 90; 90		5239.5Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157658 CIFC68 H62 N4 O13F d d 221.741; 13.765; 21.012
90; 90; 90		6288.2Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157659 CIFC32 H26 N2 O4P 1 21/c 113.8872; 9.9072; 19.4383
90; 90.026; 90		2674.38Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157660 CIFC15 H13 N O3P 1 21/c 17.0483; 9.642; 17.816
90; 93.573; 90		1208.42Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157661 CIFC14 H11 N O3P 1 21/c 111.1412; 8.63104; 12.612
90; 98.0678; 90		1200.77Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157662 CIFC14 H17 N O6C 1 2/c 123.1618; 6.1459; 20.0176
90; 95.672; 90		2835.56Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157663 CIFC20 H25 N3 O3P 1 21/c 113.962; 8.28868; 17.5984
90; 112.379; 90		1883.22Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157664 CIFC17 H21 N3P -16.7441; 9.9379; 12.0364
69.995; 75.972; 81.277		733.33Aksenov, Nicolai A.; Aksenov, Alexander V.; Kirilov, Nikita K.; Arutiunov, Nikolai A.; Aksenov, Dmitrii A.; Maslivetc, Vladimir; Zhao, Zhenze; Du, Liqin; Rubin, Michael; Kornienko, Alexander
Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity.
Organic & biomolecular chemistry, 2020, 18, 6651-6664
7157665 CIFC11 H9 N3P 1 21/c 19.1934; 10.6902; 18.2767
90; 100.449; 90		1766.43Aksenov, Nicolai A.; Aksenov, Alexander V.; Kirilov, Nikita K.; Arutiunov, Nikolai A.; Aksenov, Dmitrii A.; Maslivetc, Vladimir; Zhao, Zhenze; Du, Liqin; Rubin, Michael; Kornienko, Alexander
Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity.
Organic & biomolecular chemistry, 2020, 18, 6651-6664
7157666 CIFC134 H130 Cl6 F6 N18 O19C 2 2 2135.445; 36.434; 45.806
90; 90; 90		59154Yang, Ling; Ma, Chunmiao; Kauffmann, Brice; Li, Dongyao; Gan, Quan
Absolute handedness control of oligoamide double helices by chiral oxazolylaniline induction.
Organic & biomolecular chemistry, 2020, 18, 6643-6650
7157667 CIFC15 H30 O S2P 21 21 215.0392; 8.4897; 38.3953
90; 90; 90		1642.6Scheutz, Georg M.; Rowell, Jonathan L.; Wang, Fu-Sheng; Abboud, Khalil A.; Peng, Chi-How; Sumerlin, Brent S.
Synthesis of functional 1,2-dithiolanes from 1,3-bis-<i>tert</i>-butyl thioethers.
Organic & biomolecular chemistry, 2020, 18, 6509-6513
7157668 CIFC5 H9 O S2I 41/a :219.7501; 19.7501; 7.4965
90; 90; 90		2924.1Scheutz, Georg M.; Rowell, Jonathan L.; Wang, Fu-Sheng; Abboud, Khalil A.; Peng, Chi-How; Sumerlin, Brent S.
Synthesis of functional 1,2-dithiolanes from 1,3-bis-<i>tert</i>-butyl thioethers.
Organic & biomolecular chemistry, 2020, 18, 6509-6513
7157669 CIFC20 H18 N6P 1 21/c 15.866; 8.1481; 18.3926
90; 90; 90		879.11Rahman, Iftakur; Deka, Bhaskar; Thakuria, Ranjit; Deb, Mohit L.; Baruah, Pranjal K.
L-Proline-catalyzed regioselective C1 arylation of tetrahydroisoquinolines through a multicomponent reaction under solvent-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6514-6518
7157670 CIFC27 H28 N4P 1 21/c 113.786; 13.94; 12.043
90; 95.844; 90		2302.4Rahman, Iftakur; Deka, Bhaskar; Thakuria, Ranjit; Deb, Mohit L.; Baruah, Pranjal K.
L-Proline-catalyzed regioselective C1 arylation of tetrahydroisoquinolines through a multicomponent reaction under solvent-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6514-6518
7157671 CIFC26 H25 N5 O12P -110.0331; 11.8988; 13.4124
108; 99.413; 106.679		1401.73Luo, Yan-Long; Liu, Yu-Feng; Guan, Bing-Tao
Alkyl lithium-catalyzed benzylic C-H bond addition of alkyl pyridines to α-alkenes.
Organic & biomolecular chemistry, 2020, 18, 6622-6626
7157672 CIFC35 H32 Br Cl3 N2 O3 SP -19.5464; 11.3522; 16.3209
79.8713; 82.8439; 76.7777		1688.44Rapelli, Chandrashekhar; Sridhar, Balasubramanian; Subba Reddy, B. V.
Tandem Prins cyclization for the synthesis of indole fused spiro-1,4-diazocane scaffolds.
Organic & biomolecular chemistry, 2020, 18, 6710-6715
7157673 CIFC20 H16 N2 O SP 1 21/n 111.05; 14.7669; 11.3282
90; 109.477; 90		1742.69Song, Xiaoxiao; Xu, Lei; Ni, Qijian
Highly diastereoselective synthesis of 3-methylenetetrahydropyrans by palladium-catalyzed oxa-[4 + 2] cycloaddition of 2-alkenylbenzothiazoles.
Organic & biomolecular chemistry, 2020, 18, 6617-6621
7157674 CIFC31 H34 Br N O4P 1 21/c 110.805; 28.766; 9.1158
90; 98.138; 90		2804.8Wang, Ziyang; Huang, Anqi; Fang, Fang; Li, Pengfei; Liu, Guokai; Li, Wenjun
Non-hydrogen bond catalyst-mediated diastereoselective conjugate additions of 5H-oxazol-4-ones to o-hydroxyphenyl-substituted p-quinone methides.
Organic & biomolecular chemistry, 2020, 18, 6807-6811
7157675 CIFC34 H25 N O4P 21 21 217.2273; 12.6042; 29.1348
90; 90; 90		2654.02Mu, Yuanyang; Yuan, Yang; Wang, Ye; Xu, Murong; Feng, Ye; Zhao, Yulei; Li, Yanzhong
Synthesis of indoline-fused eight-membered azaheterocycles through Zn-catalyzed dearomatization of indoles and subsequent base-promoted C-C activation.
Organic & biomolecular chemistry, 2020, 18, 6916-6926
7157676 CIFC34 H24 Br N O4P 1 21/c 111.571; 17.156; 13.431
90; 91.359; 90		2665.5Mu, Yuanyang; Yuan, Yang; Wang, Ye; Xu, Murong; Feng, Ye; Zhao, Yulei; Li, Yanzhong
Synthesis of indoline-fused eight-membered azaheterocycles through Zn-catalyzed dearomatization of indoles and subsequent base-promoted C-C activation.
Organic & biomolecular chemistry, 2020, 18, 6916-6926
7157677 CIFC27 H27 Br N8 O5 SP 1 21/n 19.7202; 11.6843; 24.726
90; 93.705; 90		2802.4Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157678 CIFC27.5 H31 F N7 O4 SP -113.4741; 13.4934; 15.7758
84.2195; 85.3686; 76.9008		2774.41Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157679 CIFC25 H25 N7 O3 SP b c a9.7574; 16.3229; 33.1283
90; 90; 90		5276.3Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157680 CIFC27 H32 F N7 O5 SP 1 21/c 117.9516; 16.7643; 19.6754
90; 112.959; 90		5452.2Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157681 CIFC21 H21 N O3P -19.6969; 11.4348; 24.2698
85.022; 85.218; 82.945		2653.4Schendera, Eva; Villinger, Alexander; Brasholz, Malte
Photoinduced iodine-mediated tandem dehydrogenative Povarov cyclisation/C-H oxygenation reactions.
Organic & biomolecular chemistry, 2020, 18, 6912-6915
7157682 CIFC15 H18 N4 O7P 1 21 14.7625; 13.0451; 13.8262
90; 95.126; 90		855.55Nathanael, Joses G.; White, Jonathan M.; Richter, Annika; Nuske, Madison R.; Wille, Uta
Oxidative damage of proline residues by nitrate radicals (NO<sub>3</sub>˙): a kinetic and product study.
Organic & biomolecular chemistry, 2020, 18, 6949-6957
7157683 CIFC23 H17 Cl F3 NP -18.6636; 8.9777; 13.8142
83.784; 78.625; 68.828		981.4Li, Peng-Hua; Wei, Yin; Shi, Min
Cu(I)-Catalyzed addition-cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs).
Organic & biomolecular chemistry, 2020, 18, 7127-7138
7157684 CIFC27 H26 F3 NP -18.754; 13.9202; 20.4884
70.805; 84.483; 81.586		2329.4Li, Peng-Hua; Wei, Yin; Shi, Min
Cu(I)-Catalyzed addition-cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs).
Organic & biomolecular chemistry, 2020, 18, 7127-7138
7157685 CIFC24 H19 N3P 1 21/c 118.4957; 7.8032; 25.76
90; 92.571; 90		3714.1Yang, Jianhua; Xiong, Shaoqi; Ren, Yongsheng; Xiao, Tiebo; Jiang, Yubo
Copper-catalyzed cross-coupling and sequential allene-mediated cyclization for the synthesis of 1,2,3-triazolo[1,5-<i>a</i>]quinolines.
Organic & biomolecular chemistry, 2020, 18, 7174-7182
7157686 CIFC22 H24 F3 N O2P 1 21/c 118.7943; 11.2236; 9.8308
90; 95.655; 90		2063.6Ma, Rui-Jun; Sun, Jian-Ting; Liu, Chang-Hong; Chen, Ling; Si, Chang-Mei; Wei, Bang-Guo
Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to <i>N</i>,<i>O</i>-acetals.
Organic & biomolecular chemistry, 2020, 18, 7139-7150
7157687 CIFC16 H15 N O3P c c n14.3884; 26.944; 6.9828
90; 90; 90		2707.1Borgohain, Hemi; Talukdar, Kangkan; Sarma, Bipul; Das, Sajal Kumar
Regioselectivity of the trifluoroethanol-promoted intramolecular <i>N</i>-Boc-epoxide cyclization towards 1,3-oxazolidin-2-ones and 1,3-oxazinan-2-ones.
Organic & biomolecular chemistry, 2020, 18, 7401-7413
7157688 CIFC16 H15 N O3P -17.313; 9.4042; 9.8866
97.32; 95.213; 94.533		668.77Borgohain, Hemi; Talukdar, Kangkan; Sarma, Bipul; Das, Sajal Kumar
Regioselectivity of the trifluoroethanol-promoted intramolecular <i>N</i>-Boc-epoxide cyclization towards 1,3-oxazolidin-2-ones and 1,3-oxazinan-2-ones.
Organic & biomolecular chemistry, 2020, 18, 7401-7413
7157689 CIFC21 H16 N2 OP b c a14.6384; 6.909; 30.7229
90; 90; 90		3107.21Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157690 CIFC20 H12 F N2P 1 21/n 110.3439; 6.8286; 20.1913
90; 97.86; 90		1412.8Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157691 CIFC20 H13 F N2P -16.0455; 11.0023; 11.7294
112.103; 96.044; 93.256		714.87Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157692 CIFC20 H12 F2 N2P -17.8602; 8.983; 11.3189
94.775; 108.443; 100.754		736.11Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157693 CIFC22 H18 N2 O2P -15.9542; 10.6468; 13.6281
83.162; 86.529; 76.857		834.81Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157694 CIFC23 H20 N2 O3P b c a14.2321; 13.7476; 19.4973
90; 90; 90		3814.8Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157695 CIFC10 H12 I N3P b c a13.9563; 10.5922; 15.5819
90; 90; 90		2303.44Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157696 CIFC10 H12 B F4 N3P b c a14.4577; 10.5526; 15.7197
90; 90; 90		2398.3Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157697 CIFC10 H12 I3 N3C 1 2/c 120.4846; 9.4451; 15.8942
90; 99.242; 90		3035.3Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157698 CIFC31 H23 ClP 1 21/n 112.1573; 12.3663; 15.5243
90; 107.422; 90		2226.9Wei, Hao-Zhao; Li, Quan-Zhe; Wei, Yin; Shi, Min
Rapid construction of cyclopenta[<i>b</i>]naphthalene frameworks from propargylic alcohol tethered methylenecyclopropanes.
Organic & biomolecular chemistry, 2020, 18, 7396-7400
7157699 CIFC26 H21 ClP n a 2120.7442; 12.396; 7.5295
90; 90; 90		1936.17Wei, Hao-Zhao; Li, Quan-Zhe; Wei, Yin; Shi, Min
Rapid construction of cyclopenta[<i>b</i>]naphthalene frameworks from propargylic alcohol tethered methylenecyclopropanes.
Organic & biomolecular chemistry, 2020, 18, 7396-7400
7157700 CIFC1.9 H1.9 Cl0.1 F0.3 N0.1 O0.2 S0.1P -18.692; 10.4626; 12.9164
106.067; 98.907; 110.261		1017.1Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
Enantioselective addition of thiols to trifluoromethyl ketimines: synthesis of <i>N</i>,<i>S</i>-ketals.
Organic & biomolecular chemistry, 2020, 18, 7431-7436
7157701 CIFC37 H34 N2 O8 S2C 1 2 134.292; 8.1908; 16.147
90; 111.061; 90		4232.4Song, Yong-Xing; Lin, Ye; Yan, Li; Du, Da-Ming
An organocatalytic domino Michael addition strategy: construction of bispiro[oxindole-thiazolidinone-hexahydroxanthone]s with five contiguous stereocenters.
Organic & biomolecular chemistry, 2020, 18, 7373-7378
7157702 CIFC53 H80 N4 O13P 1 21 114.4086; 13.7833; 14.4694
90; 110.157; 90		2697.59Stadelmann, Thomas; Subramanian, Govindan; Menon, Sanjay; Townsend, Chad E.; Lokey, R. Scott; Ebert, Marc-Olivier; Riniker, Sereina
Connecting the conformational behavior of cyclic octadepsipeptides with their ionophoric property and membrane permeability.
Organic & biomolecular chemistry, 2020, 18, 7110-7126
7157703 CIFC118 H198 K3 N11 O36 S3P 114.9008; 15.8307; 16.8469
111.244; 101.429; 100.095		3495.22Stadelmann, Thomas; Subramanian, Govindan; Menon, Sanjay; Townsend, Chad E.; Lokey, R. Scott; Ebert, Marc-Olivier; Riniker, Sereina
Connecting the conformational behavior of cyclic octadepsipeptides with their ionophoric property and membrane permeability.
Organic & biomolecular chemistry, 2020, 18, 7110-7126
7157704 CIFC21 H21 N O3P 1 21/n 18.3648; 24.4988; 8.6463
90; 106.405; 90		1699.73Qiao, Shanshan; Qian, Peng-Cheng; Chen, Fan; Cheng, Jiang
Iron-catalyzed radical cascade 6-<i>endo</i> cyclization of dienes towards fused nitrogen heterocycles initiated by an alkoxycarbonyl radical.
Organic & biomolecular chemistry, 2020, 18, 7086-7089
7157705 CIFC27 H20 N2 O8 SP -17.6399; 11.119; 15.958
70.281; 78.966; 74.305		1221Sathi, Vidya; Thomas, Noble V.; Deepthi, Ani
Stereoselective synthesis of dispiro heterocycles by [3 + 2] cycloaddition of azomethine ylides with a thiazolo[3,2-<i>a</i>]indole derivative.
Organic & biomolecular chemistry, 2020, 18, 7822-7826
7157706 CIFC28 H21 F N2 O2 S SeP 1 21/n 113.215; 11.927; 15.344
90; 101.15; 90		2372.8Yao, Hai-Feng; Wang, Dian-Liang; Li, Fang-Hui; Wu, Bing; Cai, Zhong-Jian; Ji, Shun-Jun
Synthesis of organoselenyl isoquinolinium imides <i>via</i> iron(III) chloride-mediated tandem cyclization/selenation of <i>N</i>'-(2-alkynylbenzylidene)hydrazides and diselenides.
Organic & biomolecular chemistry, 2020, 18, 7577-7584
7157707 CIFC16 H9 Cl N2 OP 1 21/c 122.757; 4.748; 23.677
90; 104.854; 90		2472.8Chen, Junrong; Li, Zhenmin; Suleman, Muhammad; Wang, Zaibin; Lu, Ping; Wang, Yanguang
TfOH-promoted synthesis of 4,5-dihydrooxazolo[5,4-<i>c</i>]isoquinolines <i>via</i> formal [3 + 2] cycloaddition of 4-diazoisoquinolin-3-one and benzonitriles.
Organic & biomolecular chemistry, 2020, 18, 7671-7676
7157708 CIFC23 H20 N2 O SP 1 21/n 17.7469; 17.4348; 14.3624
90; 92.609; 90		1937.9Zhang, Xuxue; Liu, Chuan; Deng, Yupian; Cao, Song
Chemo- and regioselective synthesis of polysubstituted 2-aminothiophenes by the cyclization of <i>gem</i>-dibromo or <i>gem</i>-dichloroalkenes with β-keto tertiary thioamides.
Organic & biomolecular chemistry, 2020, 18, 7540-7544
7157709 CIFC18 H18 F3 N O3 SP -15.6871; 8.6686; 18.3693
81.037; 88.297; 87.959		893.7Bonciolini, Stefano; Di Filippo, Mara; Baumann, Marcus
A scalable continuous photochemical process for the generation of aminopropylsulfones.
Organic & biomolecular chemistry, 2020, 18, 9428-9432
7157710 CIFC19 H24 O6P 1 21 19.4888; 7.2783; 12.988
90; 97.094; 90		890.12Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157711 CIFC18 H24 O3P 21 21 217.0307; 8.666; 25.171
90; 90; 90		1533.6Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157712 CIFC20 H28 O2P 21 21 217.526; 13.1519; 17.4059
90; 90; 90		1722.9Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157713 CIFC19 H16 N2 O4P n a 217.6762; 12.3159; 17.1409
90; 90; 90		1620.49Choi, Jin Ho; Kim, Kunyoung; Oh, Harin; Han, Sangil; Mishra, Neeraj Kumar; Kim, In Su
Ru(ii)-Catalyzed C-H addition and oxidative cyclization of 2-aryl quinazolinones with activated aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9611-9622
7157714 CIFC37 H38 N2 O3 SP 1 21/n 112.3228; 13.5824; 19.942
90; 104.136; 90		3236.7Kumaran, Subramani; Prabhakaran, Mohan; Mariyammal, Narayanan; Parthasarathy, Kanniyappan
Catalyst-free 1,6-conjugate addition of indoles and 4-hydroxycoumarins to <i>para</i>-quinone methides: synthesis of unsymmetrical triarylmethanes.
Organic & biomolecular chemistry, 2020, 18, 7837-7841
7157715 CIFC16 H15 Br2 N5 O2P 1 21/n 118.4913; 4.7672; 19.316
90; 94.258; 90		1698.04Galve, Iñaki; Ondoño, Raül; de Rocafiguera, Claudi; Puig de la Bellacasa, Raimon; Batllori, Xavier; Puigjaner, Cristina; Font-Bardia, Mercè; Vallcorba, Oriol; Teixidó, Jordi; Borrell, José I
A captured room temperature stable Wheland intermediate as a key structure for the orthogonal decoration of 4-amino-pyrido[2,3-<i>d</i>]pyrimidin-7(8<i>H</i>)-ones.
Organic & biomolecular chemistry, 2020, 18, 9810-9815
7157716 CIFC32 H26 B2 F9 N3 O2P -111.2245; 13.0227; 13.7251
92.741; 106.371; 107.992		1810.67Moneva Lorente, Pau; Wallabregue, Antoine; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Lacour, Jérôme
Synthesis and properties of chiral fluorescent helicene-BODIPY conjugates.
Organic & biomolecular chemistry, 2020, 18, 7677-7684
7157717 CIFC15 H11 N O2P 1 21 13.9404; 16.0925; 9.1575
90; 90.254; 90		580.68Bian, Zi-Long; Lv, Xin-Xin; Li, Ya-Lan; Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Acid-promoted synthesis and photophysical properties of substituted acridine derivatives.
Organic & biomolecular chemistry, 2020, 18, 8141-8146
7157718 CIFC19 H13 N O2P n a 2118.7602; 9.1601; 16.7999
90; 90; 90		2887Bian, Zi-Long; Lv, Xin-Xin; Li, Ya-Lan; Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Acid-promoted synthesis and photophysical properties of substituted acridine derivatives.
Organic & biomolecular chemistry, 2020, 18, 8141-8146
7157719 CIFC11 H10 N OP b c a15.014; 10.0228; 21.573
90; 90; 90		3246.4Luo, Yan; Chen, Chun-Hua; Zhu, Fan; Mo, Dong-Liang
Synthesis of α-aminooxy amides through [3 + 3] cycloaddition and Sc(OTf)<sub>3</sub>-catalyzed double C-N bond cleavage in a one-pot reaction.
Organic & biomolecular chemistry, 2020, 18, 8209-8218
7157720 CIFC17 H16 N2 O2P 1 21/c 111.2384; 10.343; 13.5036
90; 107.74; 90		1495Luo, Yan; Chen, Chun-Hua; Zhu, Fan; Mo, Dong-Liang
Synthesis of α-aminooxy amides through [3 + 3] cycloaddition and Sc(OTf)<sub>3</sub>-catalyzed double C-N bond cleavage in a one-pot reaction.
Organic & biomolecular chemistry, 2020, 18, 8209-8218
7157721 CIFC14 H11 N O2P 1 21/c 110.114; 10.3178; 10.5034
90; 102.09; 90		1071.76Gangadurai, Chinnakuzhanthai; Illa, Giri Teja; Reddy, D. Srinivasa
FeCl<sub>3</sub>-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities.
Organic & biomolecular chemistry, 2020, 18, 8459-8466
7157722 CIFC37 H34 I N O2P -15.8087; 11.2608; 47.001
93.058; 90.358; 92.48		3067Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157723 CIFC23 H40 N2 OP -18.2053; 9.9516; 14.8729
79.118; 88.843; 68.605		1108.86Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157724 CIFC27 H15 F2 NP 1 21/n 15.8348; 14.7954; 21.5626
90; 92.427; 90		1859.79Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157725 CIFC17 H22 F N O3P -18.6569; 11.7473; 16.347
98.164; 91.884; 90.183		1644.6Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157726 CIFC17 H23 F2 N O3P 1 21 19.0751; 6.1933; 15.1581
90; 98.79; 90		841.95Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157727 CIFC17 H23 F2 N O3P 1 21/c 16.0625; 22.0365; 12.8581
90; 90.522; 90		1717.7Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157728 CIFC24 H21 N3 O2P 1 21/c 19.5144; 13.3582; 16.0144
90; 102.194; 90		1989.43Tang, Shi-Biao; Fu, Xiao-Pan; Wu, Gao-Rong; Zhang, Li-Li; Deng, Ke-Zuan; Yang, Jin-Yue; Xia, Cheng-Cai; Ji, Ya-Fei
Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones <i>via</i> C-H activation.
Organic & biomolecular chemistry, 2020, 18, 7922-7931
7157729 CIFC12.8 H8.8 N0.4 O0.4P -19.6741; 10.8198; 12.5635
69.234; 89.878; 72.178		1162.2Xu, Fen; Zhu, Wen-Jing; Wang, Juan; Ma, Qi; Shen, Li-Jing
Rhodium-catalyzed synthesis of substituted isoquinolones <i>via</i> a selective decarbonylation/alkyne insertion cascade of phthalimides.
Organic & biomolecular chemistry, 2020, 18, 8219-8223
7157730 CIFC16 H20 O6C 1 2 18.1628; 13.0501; 13.9274
90; 103.346; 90		1443.55Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157731 CIFC16 H20 O5P 21 21 217.2801; 9.9611; 18.9298
90; 90; 90		1372.75Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157732 CIFC16 H20 O5P 21 21 216.8403; 10.54278; 7.78736
90; 90; 90		1382.6Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157733 CIFC16 H18 O3P 21 21 217.1617; 9.7401; 18.6984
90; 90; 90		1304.32Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157734 CIFC19 H20 Cl N O5P 1 21 19.6261; 6.61723; 14.2237
90; 98.0027; 90		897.2Romaniszyn, Marta; Sieroń, Lesław; Albrecht, Łukasz
Asymmetric vinylogous Michael addition of 5-substituted-furan-2(3<i>H</i>)-ones to an α,β-unsaturated-γ-lactam.
Organic & biomolecular chemistry, 2020, 18, 8633-8637
7157735 CIFC40 H52 O11P b c n17.1752; 8.82114; 24.8611
90; 90; 90		3766.58Choo, Yvonne S. L.; Giamberini, Marta; Antonio, José; Waddell, Paul G.; Benniston, Andrew C.
Functionalized fluorescent terephthalate monomers and their attempted polyester formation.
Organic & biomolecular chemistry, 2020, 18, 8735-8745
7157736 CIFC H N OP b c a12.9152; 15.907; 18.038
90; 90; 90		3705.8Liu, Siyuan; Wang, Hang; Wang, Baomin
Catalyst-free construction of spiro [benzoquinolizidine-chromanones] <i>via</i> a tandem condensation/1,5-hydride transfer/cyclization process.
Organic & biomolecular chemistry, 2020, 18, 8839-8843
7157737 CIFC20 H14 N2 OP b c a8.3127; 17.1849; 20.9916
90; 90; 90		2998.71Jaspal, Sonam; Shinde, Vikki N.; Meena, Neha; Nipate, Dhananjay S.; Rangan, Krishnan; Kumar, Anil
Metal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids.
Organic & biomolecular chemistry, 2020, 18, 9072-9080
7157738 CIFC23 H17 N5 O2P 1 21/n 111.158; 11.434; 15.708
90; 96.925; 90		1989.4Ge, Junying; Ding, Qiuping; Yang, Man; He, Tian; Peng, Yiyuan
Copper and manganese co-mediated cascade aza-Michael addition/cyclization and azidation of 1,3-enynes: regioselective synthesis of fully substituted azido pyrroles.
Organic & biomolecular chemistry, 2020, 18, 8908-8915
7157739 CIFC18 H14 Cl N O3C 1 2/c 129.8793; 7.7831; 12.7135
90; 93.634; 90		2950.6Yugandar, Somaraju; Morita, Taiki; Nakamura, Hiroyuki
Rhodium(III)-catalysed decarboxylative C-H functionalization of isoxazoles with alkenes and sulfoxonium ylides.
Organic & biomolecular chemistry, 2020, 18, 8625-8628
7157740 CIFC26 H24 F N3P 21 21 215.6056; 17.422; 22.161
90; 90; 90		2164.3Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157741 CIFC21 H16 F N3P b c a9.2995; 9.7287; 37.4385
90; 90; 90		3387.1Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157742 CIFC24 H20 F N3 OP 1 21 15.4142; 20.89; 8.3858
90; 92.126; 90		947.8Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157743 CIFC37 H29 N O4P 110.7714; 11.3185; 13.3343
66.429; 80.647; 75.079		1436.53Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157744 CIFC36 H26 N2 O2P 3112.9632; 12.9632; 16.2424
90; 90; 120		2363.77Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157745 CIFC36 H32 N2 O2P 21 21 219.3208; 15.9714; 19.0521
90; 90; 90		2836.21Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157746 CIFC7 H7 Br N2 OP -13.8839; 8.7474; 22.667
81.742; 88.786; 85.859		760.07Li, Yibiao; Huang, Shuo; Li, Jiaming; Li, Jian; Ji, Xiaoliang; Liu, Jiasheng; Chen, Lu; Peng, Shiyong; Zhang, Kun
Access to 2-pyridinylamide and imidazopyridine from 2-fluoropyridine and amidine hydrochloride
Organic & Biomolecular Chemistry, 2020, 18, 9292-9299
7157747 CIFC12 H19 N5 O4P 1 21/c 117.8252; 7.4804; 10.9523
90; 105.159; 90		1409.56Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157748 CIFC20 H19 N5 O4P 1 21/n 114.4032; 9.8582; 19.916
90; 140.02; 90		1817Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157749 CIFC18 H17 N O4 SC 1 c 113.738; 15.885; 7.706
90; 111.13; 90		1569Ahn, Hye-In; Park, Jong-Un; Xuan, Zi; Kim, Ju Hyun
Pd-Catalyzed asymmetric [5 + 2] cycloaddition of vinylethylene carbonates and cyclic imines: access to N-fused 1,3-oxazepines.
Organic & biomolecular chemistry, 2020, 18, 9826-9830
7157750 CIFC11 H13 Cl N4 OP 14.4944; 5.4263; 12.2978
97.735; 94.192; 92.2		296.04Zhang, Yanhua; Lin, Yun; Hou, Qianqian; Liu, Xi; Pricl, Sabrina; Peng, Ling; Xia, Yi
Novel aryltriazole acyclic C-azanucleosides as anticancer candidates.
Organic & biomolecular chemistry, 2020, 18, 9689-9699
7157751 CIFC28 H25 Cl3 N2 O4 SP 1 21/n 19.9981; 15.1043; 18.6398
90; 92.173; 90		2812.85Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157752 CIFC29 H27 Cl3 N2 O4 SC 1 2/c 126.0749; 9.8982; 23.541
90; 105.383; 90		5858.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157753 CIFC21 H19 Cl N2 O3C 1 2/c 122.788; 9.824; 19.984
90; 123.49; 90		3731.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157759 CIFC16 H18 Cl N O6P 1 21/a 111.042; 8.8933; 16.9598
90; 95.377; 90		1658.12Bakthadoss, Manickam; Mushaf, Mohammad
Intramolecular [3 + 2] nitrone cycloaddition reaction: highly regio and diastereoselective synthesis of bicyclo[3.2.1]octane scaffolds.
Organic & biomolecular chemistry, 2020, 18, 9653-9659
7157760 CIFC23 H17 N OP 1 21/n 18.8725; 11.6847; 16.8773
90; 102.266; 90		1709.77Shen, Bing-Xue; Min, Xiang-Ting; Hu, Yan-Cheng; Qian, Lei-Lei; Yang, Sa-Na; Wan, Boshun; Chen, Qing-An
Copper-catalyzed boroacylation of allenes to access tetrasubstituted vinylboronates
Organic & Biomolecular Chemistry, 2020, 18, 9253-9260
7157761 CIFC27 H18 N2P 1 21/n 111.8524; 12.1284; 14.3084
90; 107.05; 90		1966.4Huang, Jian; Fu, Yang; Deng, Zhihong; Chen, Wei; Song, Zhibin; Peng, Yiyuan
Rhodium-catalyzed oxidative annulation of 1H-indazoles with alkynes for the synthesis of indazolo[3,2-a]isoquinolines via C-H bond functionalization.
Organic & biomolecular chemistry, 2020, 18, 9863-9872
7157762 CIFC26 H21 Br O5P 1 21/n 111.6835; 10.2297; 18.6723
90; 101.857; 90		2184.07Wang, Ru-Bing; Ren, Xiao-Dong; He, Jie; Zhu, Shan-Shan; Xie, Hui-Ru; Su, Guo-Zhu; Ma, Shuang-Gang; Yu, Shi-Shan
Burchellin and its stereoisomers: total synthesis, structural elucidation and antiviral activity
Organic & Biomolecular Chemistry, 2020, 18, 9081-9087
7157764 CIFC30 H26 N0.25 O4P 1 21/c 110.5825; 10.9351; 20.533
90; 94.269; 90		2369.5Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157765 CIFC152 H108 Cl12 N8 O8 SI 41/a :226.6744; 26.6744; 18.1796
90; 90; 90		12935.2Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157766 CIFC33 H21 Cl3 N2 O4P 1 21/c 114.0142; 21.038; 9.3503
90; 90.176; 90		2756.74Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157767 CIFC22 H18 Br2 Cl N O3P -18.1923; 10.0872; 13.952
75.123; 88.61; 78.866		1092.9Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157768 CIFC22 H19 Br Cl N O3P 1 21/n 115.6584; 7.2134; 19.131
90; 102.956; 90		2105.8Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157769 CIFC25 H27 N O4P 1 21/c 110.129; 15.539; 15.252
90; 105.482; 90		2313Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157770 CIFC23 H21 Br Cl N O3C 1 2/c 124.318; 9.2383; 20.24
90; 96.433; 90		4518.4Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157771 CIFC39 H53 Br N4 O4 Si3 ZnP -19.3441; 13.5093; 16.7025
98.858; 102.47; 91.92		2029.23Hayashi, Satoshi; Takamatsu, Rina; Takeda, Shiori; Noji, Masahiro; Takanami, Toshikatsu
Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins.
Organic & biomolecular chemistry, 2020, 18, 9791-9795
7157772 CIFC43 H39 N3 O8C 1 2/c 141.0905; 12.1637; 21.1598
90; 134.872; 90		7495Li, Chen-Yi; Xiang, Min; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
A base-catalyzed domino reaction between isoindigos and α-alkylidene succinimides-convenient preparation of highly steric bispirooxindoles.
Organic & biomolecular chemistry, 2020, 18, 9511-9515
7157773 CIFC17 H19 N O3 SP 15.9286; 8.2863; 8.6201
109.21; 90.208; 103.829		386.74Yang, Shuang; Chen, Yuhang; Yuan, Zidan; Bu, Feiyu; Jiang, Cheng; Ding, Zhenhua
Divergent synthesis of oxazolidines and morpholines <i>via</i> PhI(OAc)<sub>2</sub>-mediated difunctionalization of alkenes.
Organic & biomolecular chemistry, 2020, 18, 9873-9882
7157780 CIFC12 H7 N3 SP 1 n 116.216; 8.5645; 16.5649
90; 117.934; 90		2032.52Yang, Zhen; He, Jing; Wei, Yueting; Li, Weiwei; Liu, Ping; Zhao, Jixing; Wei, Yu
NCS-promoted thiocyanation and selenocyanation of pyrrolo[1,2-a]quinoxalines
Organic & Biomolecular Chemistry, 2020, 18, 9088-9094
7157781 CIFC26 H28 O8P -18.3229; 10.5201; 13.8336
88.816; 73.989; 76.976		1133.19Liu, Hongxin; Chen, Shanchong; Zhang, Xiao; Dong, Chunmao; Chen, Yuchan; Liu, Zhaoming; Tan, Haibo; Zhang, Weimin
Structural elucidation, total synthesis, and cytotoxic activity of effphenol A
Organic & Biomolecular Chemistry, 2020, 18, 9035-9038
7157782 CIFC33 H32 Br N O6P -110.102; 10.4727; 15.726
104.702; 94.205; 109.963		1489Jaiswal, Manish K.; Singh, Bhuvnesh; De, Shreemoyee; Singh, Neetu; Singh, Ravi P.
Stereoselective formal [3 + 3] annulation of 3-alkylidene-2-oxindoles with β,γ-unsaturated α-keto esters.
Organic & biomolecular chemistry, 2020, 18, 9852-9862
7157784 CIFC19 H13 N O4P 1 21/c 14.2074; 12.9179; 27.18
90; 94.001; 90		1473.7He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157785 CIFC19 H12 Br N O4P 1 21/c 112.5309; 7.1686; 17.8685
90; 94.845; 90		1599.37He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157786 CIFC40 H32P -110.4475; 12.2806; 12.3903
100.338; 99.001; 104.084		1483.14Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157787 CIFC12 H12 Br4P 1 21/c 114.8169; 23.135; 13.2408
90; 94.823; 90		4522.7Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157788 CIFC20 H38 O13 P4C 1 2/c 115.6392; 18.8539; 12.4008
90; 127.729; 90		2892Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157789 CIFC18 H24 O4P -16.9814; 11.397; 11.8876
62.708; 82.487; 73.52		806.04Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157790 CIFC12 H16 O4C 1 2/c 111.6744; 9.2737; 11.2747
90; 114.21; 90		1113.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157791 CIFC28 H30 N2P 21 21 216.859; 17.0662; 19.6709
90; 90; 90		2302.6Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157792 CIFC44 H36 N12C 1 2/c 123.8429; 14.4588; 12.002
90; 116.455; 90		3704.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157793 CIFC70 H92 O26P 6511.0913; 11.0913; 92.9928
90; 90; 120		9907.06Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157794 CIFC26 H32 O7P 21 21 218.0223; 13.6842; 21.6959
90; 90; 90		2381.75Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157795 CIFC18 H18 N4 O4P 1 21/c 111.1364; 19.9122; 8.5927
90; 107.324; 90		1819Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157796 CIFC18 H18 N2 O3P 1 21/n 110.3803; 7.9121; 19.5926
90; 104.061; 90		1560.93Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157797 CIFC27 H21 Cl F3 N O7P 1 21/n 113.5978; 14.619; 13.9308
90; 117.095; 90		2465.33Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157798 CIFC28 H26 F3 N3 O6P 1 21 18.8532; 13.7373; 11.5286
90; 107.761; 90		1335.27Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157799 CIFC22 H21 N O2 S2P 1 21/n 18.0525; 15.8806; 15.2504
90; 94.189; 90		1945Wu, Jia-Yu; Liao, Wei-Jr; Lin, Xiu-Yi; Liang, Chien-Fu
A facile access to <i>N</i>-sulfonylthioimidates and their use for the transformation to 3,4-dihydroquinazolines.
Organic & biomolecular chemistry, 2020, 18, 8881-8885
7157800 CIFC20 H14 Cl N OP -18.0991; 10.0866; 10.5705
75.779; 69.449; 67.461		740.63Zheng, Jing; He, Xiaojie; Xu, Hong; Liu, Hua; Yang, Weiran
A formal [3 + 2] annulation reaction of propargyl sulfonium compounds and <i>N</i>-ylides: access to pyrrolo[2,1-<i>a</i>]quinolines, pyrrolo[2,1-<i>a</i>]phthalazines and indolizines.
Organic & biomolecular chemistry, 2020, 18, 8867-8875
7157801 CIFC2.5 H2 Cl0.33 O0.67P 1 21/c 111.3742; 18.028; 7.5166
90; 106.736; 90		1476.02Xie, Zhen-Zhen; Deng, Zhi-Xiong; Zheng, Yu; Chen, Yan-Shan; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-mediated domino sequence of salicylaldehyde with but-3-yn-2-one: rapid access to chromanone.
Organic & biomolecular chemistry, 2020, 18, 8916-8920
7157802 CIFC24 H19 Br N2 O3 SP -18.1722; 10.5252; 13.3654
80.905; 79.401; 76.274		1089.82Feng, Jiajun; He, Tiantong; Xie, Yuxing; Yu, Yang; Baell, Jonathan B.; Huang, Fei
I<sub>2</sub>-Promoted [4 + 2] cycloaddition of <i>in situ</i> generated azoalkenes with enaminones: facile and efficient synthesis of 1,4-dihydropyridazines and pyridazines.
Organic & biomolecular chemistry, 2020, 18, 9483-9493
7201564 CIFC82.75 H53.5 Cl1.5 N4 O2.5P -113.22; 13.543; 19.421
99.88; 102.01; 96.01		3314.8Xu, Xinjun; Yu, Gui; Chen, Shiyan; Di, Chong'an; Liu, Yunqi
Synthesis and characterization of a quinoxaline compound containing polyphenylphenyl and strong electron-accepting groups, and its multiple applications in electroluminescent devices
Journal of Materials Chemistry, 2008, 18, 299
7201667 CIFC12 H14 O4 ZnC 1 c 17.81357; 20.39273; 6.849
90; 92.4813; 90		1090.3Nielsen, Renie Birkedal; Kongshaug, Kjell Ove; Fjellvåg, Helmer
Delamination, synthesis, crystal structure and thermal properties of the layered metal-organic compound Zn(C12H14O4)
Journal of Materials Chemistry, 2008, 18, 1002
7201721 CIFC89.6 H76.4 Cl18 Cu6 N6 O43R -3 c :H22.3534; 22.3534; 41.1462
90; 90; 120		17805.2Roques, Nans; Maspoch, Daniel; Luis, Fernando; Camón, Agustín; Wurst, Klaus; Datcu, Angela; Rovira, Concepció; Ruiz-Molina, Daniel; Veciana, Jaume
A hexacarboxylic open-shell building block: synthesis, structure and magnetism of a three-dimensional metal‒radical framework
Journal of Materials Chemistry, 2008, 18, 98
7201722 CIFC98 H94 Cl18 Cu6 N6 O40R -3 c :H22.4479; 22.4479; 41.172
90; 90; 120		17967.4Roques, Nans; Maspoch, Daniel; Luis, Fernando; Camón, Agustín; Wurst, Klaus; Datcu, Angela; Rovira, Concepció; Ruiz-Molina, Daniel; Veciana, Jaume
A hexacarboxylic open-shell building block: synthesis, structure and magnetism of a three-dimensional metal‒radical framework
Journal of Materials Chemistry, 2008, 18, 98
7201731 CIFC35 H37 N O10 PtP -110.484; 10.86; 14.752
93.617; 104.214; 98.912		1599.5Venkatesan, Koushik; Kouwer, Paul H. J.; Yagi, Shigeyuki; Müller, Peter; Swager, Timothy M.
Columnar mesophases from half-discoid platinum cyclometalated metallomesogens
Journal of Materials Chemistry, 2008, 18, 400
7201732 CIFC31 H31 Cl2 N O8 Pt SC 1 c 120.996; 10.4617; 15.1265
90; 112.473; 90		3070.3Venkatesan, Koushik; Kouwer, Paul H. J.; Yagi, Shigeyuki; Müller, Peter; Swager, Timothy M.
Columnar mesophases from half-discoid platinum cyclometalated metallomesogens
Journal of Materials Chemistry, 2008, 18, 400
7201733 CIFC20 H12 Ni S8P 1 21/n 112.112; 5.4414; 17.026
90; 110.51; 90		1051Anjos, Tania; Roberts-Bleming, Susan J.; Charlton, Adam; Robertson, Neil; Mount, Andrew R.; Coles, Simon J.; Hursthouse, Michael B.; Kalaji, Maher; Murphy, Patrick J.
Nickel dithiolenes containing pendant thiophene units: precursors to dithiolene‒polythiophene hybrid materials
Journal of Materials Chemistry, 2008, 18, 475
7201734 CIFC20 H12 Ni S8P -19.5217; 9.81; 11.985
90.14; 100.37; 93.73		1098.8Anjos, Tania; Roberts-Bleming, Susan J.; Charlton, Adam; Robertson, Neil; Mount, Andrew R.; Coles, Simon J.; Hursthouse, Michael B.; Kalaji, Maher; Murphy, Patrick J.
Nickel dithiolenes containing pendant thiophene units: precursors to dithiolene‒polythiophene hybrid materials
Journal of Materials Chemistry, 2008, 18, 475
7201752 CIFC50 H34 N2 SP -16.0191; 9.059; 17.191
100.69; 95.305; 91.741		916.1Wei, Peng; Duan, Lian; Zhang, Deqiang; Qiao, Juan; Wang, Liduo; Wang, Ruji; Dong, Guifang; Qiu, Yong
A new type of light-emitting naphtho[2,3-c][1,2,5]thiadiazole derivatives: synthesis, photophysical characterization and transporting properties
Journal of Materials Chemistry, 2008, 18, 806
7201753 CIFC34 H22 N2 SC 1 2/c 19.3698; 28.45; 9.4857
90; 107.178; 90		2415.8Wei, Peng; Duan, Lian; Zhang, Deqiang; Qiao, Juan; Wang, Liduo; Wang, Ruji; Dong, Guifang; Qiu, Yong
A new type of light-emitting naphtho[2,3-c][1,2,5]thiadiazole derivatives: synthesis, photophysical characterization and transporting properties
Journal of Materials Chemistry, 2008, 18, 806
7201779 CIFC26 H41 Cr Mn N3 O14P 639.41; 9.41; 17.809
90; 90; 120		1365.7Coronado, Eugenio; Giménez-Saiz, Carlos; Gómez-García, Carlos J.; Romero, Francisco M.; Tarazón, Ana
Layered ferromagnets hosting tetraalkylammonium-substituted nitronyl nitroxide free radicals
Journal of Materials Chemistry, 2008, 18, 929
7201782 CIFC41 H36 N4 S2C 1 2/c 133.557; 15.363; 13.991
90; 98.497; 90		7134Qi, Ting; Liu, Yunqi; Qiu, Wenfeng; Zhang, Hengjun; Gao, Xike; Liu, Ying; Lu, Kun; Du, Chunyan; Yu, Gui; Zhu, Daoben
Synthesis and properties of fluorene or carbazole-based and dicyanovinyl-capped n-type organic semiconductors
Journal of Materials Chemistry, 2008, 18, 1131
7201801 CIFC H3 B Cl5 N SiP 1 21/m 17.0996; 6.8561; 8.9728
90; 94.854; 90		435.19Weinmann, Markus; Kroschel, Matthias; Jäschke, Thomas; Nuss, Jürgen; Jansen, Martin; Kolios, Grigorios; Morillo, Aristides; Tellaeche, Carlos; Nieken, Ulrich
Towards continuous processes for the synthesis of precursors of amorphous Si/B/N/C ceramics
Journal of Materials Chemistry, 2008, 18, 1810
7201820 CIFC68 H89 O19 Sn6P -112.585; 12.9929; 14.2161
110.801; 114.727; 97.63		1862.3Delavaux-Nicot, Béatrice; Kaeser, Adrien; Hahn, Uwe; Gégout, Aline; Brandli, Pierre-Elie; Duhayon, Carine; Coppel, Yannick; Saquet, Alix; Nierengarten, Jean-François
Organotin chemistry for the preparation of fullerene-rich nanostructures
Journal of Materials Chemistry, 2008, 18, 1547
7201826 CIFC32 H33 Cl6 N S SbP 1 21/a 113.7062; 21.5592; 22.5411
90; 94.493; 90		6640.3Oka, Hiroyuki
Synthesis and through-bond spin interaction of stable 1,3-phenylene linked poly(phenothiazine cation radical)
Journal of Materials Chemistry, 2008, 18, 1927
7201834 CIFC34 H30P 1 21/c 119.8513; 5.3006; 22.6989
90; 93.5526; 90		2383.87Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201835 CIFC38 H38P -16.6368; 8.3446; 13.7421
105.526; 100.252; 92.736		717.92Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201836 CIFC36 H34P 1 21/n 112.3212; 5.142; 20.803
90; 101.16; 90		1293.06Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201837 CIFC54 H74 Si2P -18.8577; 11.129; 12.5975
101.919; 93.8211; 101.29		1184.1Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201838 CIFC46 H58 Si2P 1 21/c 18.884; 22.324; 10.797
90; 110.146; 90		2010.32Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201839 CIFC42 H50 Si2P -110.6177; 13.6171; 14.0829
75.154; 73.915; 71.123		1819.86Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201840 CIFC50 H66 Si2P b c a10.3715; 15.4649; 27.5066
90; 90; 90		4411.9Chen, Jihua; Subramanian, Sankar; Parkin, Sean R.; Siegler, Maxime; Gallup, Kaitlin; Haughn, Chelsea; Martin, David C.; Anthony, John E.
The influence of side chains on the structures and properties of functionalized pentacenes
Journal of Materials Chemistry, 2008, 18, 1961
7201871 CIFC9 H8 O2 S4P 1 21/n 127.474; 11.463; 7.459
90; 96.485; 90		2334.1Shao, Xiangfeng; Nakano, Yoshiaki; Yamochi, Hideki; Dubrovskiy, Alexander D.; Otsuka, Akihiro; Murata, Tsuyoshi; Yoshida, Yukihiro; Saito, Gunzi; Koshihara, Shin-ya
Formation of two-dimensional metals by weak intermolecular interactions based on the asymmetric EDO-TTF derivatives
Journal of Materials Chemistry, 2008, 18, 2131
7201872 CIFC9 H8 O2 S5P b c a13.681; 17.438; 10.53
90; 90; 90		2512.1Shao, Xiangfeng; Nakano, Yoshiaki; Yamochi, Hideki; Dubrovskiy, Alexander D.; Otsuka, Akihiro; Murata, Tsuyoshi; Yoshida, Yukihiro; Saito, Gunzi; Koshihara, Shin-ya
Formation of two-dimensional metals by weak intermolecular interactions based on the asymmetric EDO-TTF derivatives
Journal of Materials Chemistry, 2008, 18, 2131
7201873 CIFC18 H16 B F4 O4 S8C m c m28.752; 12.369; 6.969
90; 90; 90		2478.4Shao, Xiangfeng; Nakano, Yoshiaki; Yamochi, Hideki; Dubrovskiy, Alexander D.; Otsuka, Akihiro; Murata, Tsuyoshi; Yoshida, Yukihiro; Saito, Gunzi; Koshihara, Shin-ya
Formation of two-dimensional metals by weak intermolecular interactions based on the asymmetric EDO-TTF derivatives
Journal of Materials Chemistry, 2008, 18, 2131
7201874 CIFC18 H16 Cl O8 S8C m c m29.107; 12.412; 6.962
90; 90; 90		2515.2Shao, Xiangfeng; Nakano, Yoshiaki; Yamochi, Hideki; Dubrovskiy, Alexander D.; Otsuka, Akihiro; Murata, Tsuyoshi; Yoshida, Yukihiro; Saito, Gunzi; Koshihara, Shin-ya
Formation of two-dimensional metals by weak intermolecular interactions based on the asymmetric EDO-TTF derivatives
Journal of Materials Chemistry, 2008, 18, 2131
7201916 CIFC112 H92 N22 Ni5 S20P -17.9605; 17.0682; 22.327
69.628; 89.239; 79.236		2789.4Lopes, Elsa B.; Alves, Helena; Santos, Isabel C.; Graf, David; Brooks, James S.; Canadell, Enric; Almeida, Manuel
The family of molecular conductors [(n-Bu)4N]2[M(dcbdt)2]5, M = Cu, Ni, Au; band filling and stacking modulation effects
Journal of Materials Chemistry, 2008, 18, 2825
7201917 CIFC112 H92 Au5 N22 S20P -17.973; 17.322; 23.171
68.119; 88.882; 78.409		2903.6Lopes, Elsa B.; Alves, Helena; Santos, Isabel C.; Graf, David; Brooks, James S.; Canadell, Enric; Almeida, Manuel
The family of molecular conductors [(n-Bu)4N]2[M(dcbdt)2]5, M = Cu, Ni, Au; band filling and stacking modulation effects
Journal of Materials Chemistry, 2008, 18, 2825
7201918 CIFC112 H92 Au5 N22 S20P -17.9351; 17.0822; 22.9746
68.763; 88.809; 78.163		2836.08Lopes, Elsa B.; Alves, Helena; Santos, Isabel C.; Graf, David; Brooks, James S.; Canadell, Enric; Almeida, Manuel
The family of molecular conductors [(n-Bu)4N]2[M(dcbdt)2]5, M = Cu, Ni, Au; band filling and stacking modulation effects
Journal of Materials Chemistry, 2008, 18, 2825
7201956 CIFC66 H48 Cl3 Ir N6 O3P 1 21/c 115.6727; 20.528; 17.462
90; 91.444; 90		5616.3Tong, Bihai; Mei, Qunbo; Wang, Shuanjin; Fang, Yuan; Meng, Yuezhong; Wang, Biao
Nearly 100% internal phosphorescence efficiency in a polymer light-emitting diode using a new iridium complex phosphor
Journal of Materials Chemistry, 2008, 18, 1636
7201966 CIFC24 H14 S2P -15.916; 7.78; 18.02
85.34; 98.25; 93.72		817Mamada, Masashi; Nishida, Jun-ichi; Kumaki, Daisuke; Tokito, Shizuo; Yamashita, Yoshiro
High performance organic field-effect transistors based on [2,2′]bi[naphtho[2,3-b]thiophenyl] with a simple structure
Journal of Materials Chemistry, 2008, 18, 3442
7202021 CIFC73 H169 Ag6 Cl3 N6 P12 S12P 1 21/c 125.5883; 14.0036; 33.5098
90; 107.722; 90		11437.7Panneerselvam, Arunkumar; Malik, Mohammad A.; O'Brien, Paul; Raftery, James
The CVD of silver sulfide and silver thin films from a homoleptic crystalline single-source precursor
Journal of Materials Chemistry, 2008, 18, 3264
7202074 CIFC58 H46 SiP b c n17.034; 10.422; 24.427
90; 90; 90		4336Zhan, Xiaowei; Haldi, Andreas; Risko, Chad; Chan, Calvin K.; Zhao, Wei; Timofeeva, Tatiana V.; Korlyukov, Aleksander; Antipin, Mikhail Yu.; Montgomery, Sarah; Thompson, Evans; An, Zesheng; Domercq, Benoit; Barlow, Stephen; Kahn, Antoine; Kippelen, Bernard; Brédas, Jean-Luc; Marder, Seth R.
Fluorenyl-substituted silole molecules: geometric, electronic, optical, and device properties
Journal of Materials Chemistry, 2008, 18, 3157
7202075 CIFC47 H34 SiP 1 21/c 113.448; 10.218; 25.111
90; 97.34; 90		3422.3Zhan, Xiaowei; Haldi, Andreas; Risko, Chad; Chan, Calvin K.; Zhao, Wei; Timofeeva, Tatiana V.; Korlyukov, Aleksander; Antipin, Mikhail Yu.; Montgomery, Sarah; Thompson, Evans; An, Zesheng; Domercq, Benoit; Barlow, Stephen; Kahn, Antoine; Kippelen, Bernard; Brédas, Jean-Luc; Marder, Seth R.
Fluorenyl-substituted silole molecules: geometric, electronic, optical, and device properties
Journal of Materials Chemistry, 2008, 18, 3157
7202097 CIFC4 H14 B2 Cl6 N2 Si2P b c a8.76; 13.344; 13.754
90; 90; 90		1607.8Müller, Utz; Weinmann, Markus; Jansen, Martin
Cl2MeSi‒NH‒BCl2 and ClMe2Si‒NH‒BCl2: novel processable single source precursors of amorphous Si/C/B/N ceramics
Journal of Materials Chemistry, 2008, 18, 3671
7202102 CIFC18 H14 N4 O4P 1 21/n 16.4194; 8.268; 15.213
90; 92.69; 90		806.5Qu, Songnan; Chen, Xiaofang; Shao, Xiang; Li, Fan; Zhang, Hongyu; Wang, Haitao; Zhang, Peng; Yu, Zhixin; Wu, Kai; Wang, Yue; Li, Min
Self-assembly of highly luminescent bi-1,3,4-oxadiazole derivatives through electron donor‒acceptor interactions in three-dimensional crystals, two-dimensional layers and mesophases
Journal of Materials Chemistry, 2008, 18, 3954
7202144 CIFC36 H21 Cl2 F6 Ir N6C 1 2/c 126.1732; 15.7673; 18.1899
90; 117.832; 90		6638.26Orselli, Enrico; Albuquerque, Rodrigo Q.; Fransen, P. Michel; Fröhlich, Roland; Janssen, Henk M.; De Cola, Luisa
1,2,3-Triazolyl-pyridine derivatives as chelating ligands for blue iridium(iii) complexes. Photophysics and electroluminescent devices
Journal of Materials Chemistry, 2008, 18, 4579
7202145 CIFC39 H24 F9 Ir N6 OC 1 2/c 125.9847; 16.2224; 18.3429
90; 116.537; 90		6917.55Orselli, Enrico; Albuquerque, Rodrigo Q.; Fransen, P. Michel; Fröhlich, Roland; Janssen, Henk M.; De Cola, Luisa
1,2,3-Triazolyl-pyridine derivatives as chelating ligands for blue iridium(iii) complexes. Photophysics and electroluminescent devices
Journal of Materials Chemistry, 2008, 18, 4579
7202174 CIFC78.5 H49 ClP -115.3491; 15.7065; 15.7888
66.033; 61.608; 62.436		2882.6Wang, Lei; Wong, Wai-Yeung; Lin, Mei-Fang; Wong, Wai-Kwok; Cheah, Kok-Wai; Tam, Hoi-Lam; Chen, Chin H.
Novel host materials for single-component white organic light-emitting diodes based on 9-naphthylanthracene derivatives
Journal of Materials Chemistry, 2008, 18, 4529
7202178 CIF?P m -3 m4.20533; 4.20533; 4.20533
90; 90; 90		74.3704Azad, Abul K.; Savaniu, Cristian; Tao, Shanwen; Duval, Sophie; Holtappels, Peter; Ibberson, Richard M.; Irvine, John T. S.
Structural origins of the differing grain conductivity values in BaZr0.9Y0.1O2.95 and indication of novel approach to counter defect association
Journal of Materials Chemistry, 2008, 18, 3414
7202179 CIFBa O2.68 Y0.1 Zr0.9P m -3 m4.19943; 4.19943; 4.19943
90; 90; 90		74.0578Azad, Abul K.; Savaniu, Cristian; Tao, Shanwen; Duval, Sophie; Holtappels, Peter; Ibberson, Richard M.; Irvine, John T. S.
Structural origins of the differing grain conductivity values in BaZr0.9Y0.1O2.95 and indication of novel approach to counter defect association
Journal of Materials Chemistry, 2008, 18, 3414
7202196 CIFC34 H38 N2 O5 P SP -112.042; 12.306; 11.691
95.75; 111.52; 83.2		1597.3Akutsu, Hiroki; Sato, Keiko; Yamashita, Shinji; Yamada, Jun-ichi; Nakatsuji, Shin'ichi; Turner, Scott S.
The first organic paramagnetic metal containing the aminoxyl radical
Journal of Materials Chemistry, 2008, 18, 3313
7202197 CIFC30 H34 N2 O5 S17P -112.436; 19.528; 9.326
97.06; 110.22; 83.44		2102.9Akutsu, Hiroki; Sato, Keiko; Yamashita, Shinji; Yamada, Jun-ichi; Nakatsuji, Shin'ichi; Turner, Scott S.
The first organic paramagnetic metal containing the aminoxyl radical
Journal of Materials Chemistry, 2008, 18, 3313
7202225 CIFC15 H20 O ZrP 1 21/n 17.6566; 14.2184; 12.4639
90; 91.546; 90		1356.4Black, Kate; Aspinall, Helen C.; Jones, Anthony C.; Przybylak, Katarzyna; Bacsa, John; Chalker, Paul R.; Taylor, Stephen; Zhao, Ce Zhou; Elliott, Simon D.; Zydor, Aleksandra; Heys, Peter N.
Deposition of ZrO2 and HfO2 thin films by liquid injection MOCVD and ALD using ansa-metallocene zirconium and hafnium precursors
Journal of Materials Chemistry, 2008, 18, 4561
7202226 CIFC15 H20 HfP 1 21/m 17.17; 9.053; 10.385
90; 91.14; 90		674Black, Kate; Aspinall, Helen C.; Jones, Anthony C.; Przybylak, Katarzyna; Bacsa, John; Chalker, Paul R.; Taylor, Stephen; Zhao, Ce Zhou; Elliott, Simon D.; Zydor, Aleksandra; Heys, Peter N.
Deposition of ZrO2 and HfO2 thin films by liquid injection MOCVD and ALD using ansa-metallocene zirconium and hafnium precursors
Journal of Materials Chemistry, 2008, 18, 4561
7202282 CIFC16 H9 N3 S2P 1 21/n 14.7896; 23.389; 11.493
90; 97.35; 90		1276.9Hong, Wei; Wei, Zhongming; Xi, Hongxia; Xu, Wei; Hu, Wenping; Wang, Quanrui; Zhu, Daoben
6H-Pyrrolo[3,2-b:4,5-b′]bis[1,4]benzothiazines: facilely synthesized semiconductors for organic field-effect transistors
Journal of Materials Chemistry, 2008, 18, 4814
7202384 CIFC2 H5 N9 OP 1 21/c 19.3669; 10.531; 6.8081
90; 90.42; 90		671.6Klapötke, Thomas M.; Mayer, Peter; Stierstorfer, Jörg; Weigand, Jan J.
Bistetrazolylamines—synthesis and characterization
Journal of Materials Chemistry, 2008, 18, 5248
7202385 CIFC4 H11 N9 O2 SC 1 2/c 115.933; 6.8863; 19.9204
90; 104.227; 90		2118.6Klapötke, Thomas M.; Mayer, Peter; Stierstorfer, Jörg; Weigand, Jan J.
Bistetrazolylamines—synthesis and characterization
Journal of Materials Chemistry, 2008, 18, 5248
7202386 CIFC5 H9 N9P 1 21/m 13.852; 19.395; 5.769
90; 95.6; 90		428.9Klapötke, Thomas M.; Mayer, Peter; Stierstorfer, Jörg; Weigand, Jan J.
Bistetrazolylamines—synthesis and characterization
Journal of Materials Chemistry, 2008, 18, 5248
7202387 CIFC4 H7 N9P 1 21/c 110.279; 11.338; 6.772
90; 94.74; 90		786.5Klapötke, Thomas M.; Mayer, Peter; Stierstorfer, Jörg; Weigand, Jan J.
Bistetrazolylamines—synthesis and characterization
Journal of Materials Chemistry, 2008, 18, 5248
7202388 CIFC2 H3 N9P b c a11.109; 9.2272; 21.327
90; 90; 90		2186.1Klapötke, Thomas M.; Mayer, Peter; Stierstorfer, Jörg; Weigand, Jan J.
Bistetrazolylamines—synthesis and characterization
Journal of Materials Chemistry, 2008, 18, 5248
7202399 CIFC3 H10 N10P 21 21 215.6667; 9.4916; 15.9768
90; 90; 90		859.33Tao, Guo-Hong; Guo, Yong; Joo, Young-Hyuk; Twamley, Brendan; Shreeve, Jean'ne M.
Energetic nitrogen-rich salts and ionic liquids: 5-aminotetrazole (AT) as a weak acid
Journal of Materials Chemistry, 2008, 18, 5524
7209475 CIFB P S4I 2 2 25.6; 5.25; 9.04
90; 90; 90		265.776Schaefer, H.; Weiss, A.
Zur Kenntnis von Bortetrathiophosphat B P S4
Zeitschrift fuer Naturforschung, Teil B. Anorganische Chemie, Organische Chemie (2,1947-32,1977), 1963, 18, 81-82
7220499 CIFC8 H8 O3P n a 2116.3977; 3.8099; 45.645
90; 90; 90		2851.61Kavuru, Padmini; Grebinoski, Stephanie J.; Patel, Mitulkumar A.; Wojtas, Lukasz; Chadwick, Keith
Polymorphism of vanillin revisited: the discovery and selective crystallization of a rare crystal structure
CrystEngComm, 2016, 18, 1118
7221876 CIFC19 H11 N O2 SP 1 21/c 112.242; 11.566; 10.526
90; 93.08; 90		1488.2Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri
Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones
Green Chem., 2016, 18, 402
7221978 CIFC4 H6 O4P 1 21/c 110.6016; 9.5305; 10.7702
90; 119.312; 90		948.88Tryznowski, M.; Żołek-Tryznowska, Z.; Świderska, A.; Parzuchowski, P. G.
Synthesis, characterization and reactivity of a six-membered cyclic glycerol carbonate bearing a free hydroxyl group
Green Chem., 2016, 18, 802
7222111 CIFC18 H31 N O4P -19.384; 10.484; 11.281
102.829; 94.191; 113.456		976.4Maleki, Abbas; Nematollahi, Davood; Rasouli, Fereshteh; Zeinodini-Meimand, Azam
Electrode instead of catalyst and enzyme. A greener protocol for the synthesis of new 2-hydroxyacetamide derivatives containing a γ-lactone ring
Green Chem., 2016, 18, 672
7222902 CIFAs H12 N3 S4P n m a9.21; 11.03; 9.58
90; 90; 90		973.197Schaefer, H.; Weiss, A.; Schaefer, G.
Die Kristallstruktur von Ammoniumtetrathioarsenat (N H4)3 As S4
Zeitschrift fuer Naturforschung, Teil B. Anorganische Chemie, Organische Chemie (2,1947-32,1977), 1963, 18, 665-665
7222916 CIFC7 H10 F N O3P 1 21 18.5224; 10.305; 9.1442
90; 90.3404; 90		803.06Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222917 CIFC7 H10 F N O3P 1 21 18.5211; 10.3039; 9.1547
90; 90.365; 90		803.77Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222918 CIFC8 H15 Cl F N O4P -15.821; 6.4875; 15.7485
100.738; 96.625; 94.612		577.23Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222919 CIFC7 H10 F N O3P 1 21/c 112.256; 6.72544; 10.4787
90; 113.193; 90		793.92Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222920 CIFC7 H13 Cl F N O4P 1 21/c 112.235; 11.3068; 7.6415
90; 100.289; 90		1040.12Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222921 CIFC6 H10 F N O4P -16.5648; 6.6759; 9.6206
98.163; 100.929; 101.047		399.3Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7223177 CIFC18 H16 N6 O6 ZnC 1 2/c 113.519; 9.896; 14.609
90; 112.259; 90		1808.8Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223178 CIFC10 H10 Cl N3 O3 ZnP 1 21/c 19.097; 17.622; 7.464
90; 92.337; 90		1195.5Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223179 CIFC18 H12 N6 O4 ZnC 1 2 113.664; 7.8616; 8.2311
90; 91.4; 90		883.9Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223180 CIFC21 H26.2 Cd N7 O8.6P n c 28.3848; 14.808; 11.494
90; 90; 90		1427.1Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223181 CIFC18 H12 Cd N6 O4F d d 216.68; 32.764; 6.5537
90; 90; 90		3581.6Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223182 CIFC58.5 H54.5 Cd5 Cl4 N19.5 O17.5P -112.946; 17.321; 22.153
70.13; 76.08; 73.31		4418.3Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223183 CIFC22 H28 N7 O8.5 ZnP b c n20.0621; 15.593; 17.2349
90; 90; 90		5391.6Yang, Li-Bo; Wang, Hong-Can; Fang, Xiao-Dan; Chen, Si-Jin; Xu, Quan-Qing; Zhu, Ai-Xin; Yang, Zhi
A series of Zn(ii) and Cd(ii) coordination compounds based on 4-(4H-1,2,4-triazol-4-yl)benzoic acid: synthesis, structure and photoluminescence properties
CrystEngComm, 2016, 18, 130
7223199 CIFC8 H10 Cl N5P -114.916; 14.964; 15.309
64.365; 89.997; 62.904		2659Jang, Yoona; Yoo, Seo Yeon; Gu, Hye Rin; Lee, Yu Jin; Cha, Young Shin; You, Laekyeong; Noh, Kyungkyou; Kim, Jaheon
Hydrogen-bonding networks of purine derivatives and their bilayers for guest intercalation
CrystEngComm, 2016, 18, 62
7223200 CIFC20 H28 Cl2 N10P -115.078; 15.132; 21.864
81.61; 80.08; 89.95		4859.8Jang, Yoona; Yoo, Seo Yeon; Gu, Hye Rin; Lee, Yu Jin; Cha, Young Shin; You, Laekyeong; Noh, Kyungkyou; Kim, Jaheon
Hydrogen-bonding networks of purine derivatives and their bilayers for guest intercalation
CrystEngComm, 2016, 18, 62
7223201 CIFC24 H30 Cl2 N10C c c a :215.022; 44.14; 15.211
90; 90; 90		10086Jang, Yoona; Yoo, Seo Yeon; Gu, Hye Rin; Lee, Yu Jin; Cha, Young Shin; You, Laekyeong; Noh, Kyungkyou; Kim, Jaheon
Hydrogen-bonding networks of purine derivatives and their bilayers for guest intercalation
CrystEngComm, 2016, 18, 62
7223202 CIFC88 H72 Cd5 N6 O28P 1 21/c 114.6261; 23.2526; 15.7357
90; 107.099; 90		5115.1Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223203 CIFC96 H82 Cd5 N8 O28P 1 21/c 114.5196; 23.367; 15.6042
90; 107.475; 90		5049.8Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223204 CIFC88 H72 Cd3 Cu2 N6 O27P 1 21/c 114.3997; 23.362; 15.543
90; 106.309; 90		5018.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223205 CIFC90 H76 Cd5 N6 O28P 1 21/c 114.583; 23.241; 15.6338
90; 106.99; 90		5067.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223238 CIFC52 H30 Gd2 N4 Na2 O21 ZnI m m a27.631; 29.08; 13.136
90; 90; 90		10554.9Tripuramallu, Bharat Kumar; Titi, Hatem M.; Roy, Sadipan; Verma, Roli; Goldberg, Israel
Ameliorated synthetic methodology for crystalline lanthanoid‒metalloporphyrin open frameworks based on a multitopic octacarboxy-porphyrin scaffold: structural, gas sorption and photophysical properties
CrystEngComm, 2016, 18, 515
7223239 CIFC52 H30 N4 Na2 O21 Sm2 ZnI m m a27.108; 29.418; 12.9723
90; 90; 90		10345Tripuramallu, Bharat Kumar; Titi, Hatem M.; Roy, Sadipan; Verma, Roli; Goldberg, Israel
Ameliorated synthetic methodology for crystalline lanthanoid‒metalloporphyrin open frameworks based on a multitopic octacarboxy-porphyrin scaffold: structural, gas sorption and photophysical properties
CrystEngComm, 2016, 18, 515
7223240 CIFC52 H29 Dy2 N4 Na2 O21 ZnI m m a27.1337; 29.2422; 13.0757
90; 90; 90		10374.9Tripuramallu, Bharat Kumar; Titi, Hatem M.; Roy, Sadipan; Verma, Roli; Goldberg, Israel
Ameliorated synthetic methodology for crystalline lanthanoid‒metalloporphyrin open frameworks based on a multitopic octacarboxy-porphyrin scaffold: structural, gas sorption and photophysical properties
CrystEngComm, 2016, 18, 515
7223241 CIFC52 H34 Eu2 N4 Na2 O21 ZnI m m a27.4347; 28.9058; 13.1157
90; 90; 90		10401Tripuramallu, Bharat Kumar; Titi, Hatem M.; Roy, Sadipan; Verma, Roli; Goldberg, Israel
Ameliorated synthetic methodology for crystalline lanthanoid‒metalloporphyrin open frameworks based on a multitopic octacarboxy-porphyrin scaffold: structural, gas sorption and photophysical properties
CrystEngComm, 2016, 18, 515
7223242 CIFK2 Mg Mo8 O32 Th3C 1 2/c 118.568; 18.0282; 9.4188
90; 90.35; 90		3152.9Xiao, Bin; Schlenz, Hartmut; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
The structural effects of alkaline- and rare-earth element incorporation into thorium molybdates
CrystEngComm, 2016, 18, 113
7223243 CIFK2 Mo6 O24 Sr Th2P -18.0197; 8.447; 16.03
101.55; 102.893; 97.388		1019.9Xiao, Bin; Schlenz, Hartmut; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
The structural effects of alkaline- and rare-earth element incorporation into thorium molybdates
CrystEngComm, 2016, 18, 113
7223244 CIFMo18 Nd4 O72 Th6P 63/m17.556; 17.556; 6.2713
90; 90; 120		1673.9Xiao, Bin; Schlenz, Hartmut; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
The structural effects of alkaline- and rare-earth element incorporation into thorium molybdates
CrystEngComm, 2016, 18, 113
7223245 CIFMg Mo8 O32 Rb2 Th3C 1 2/c 118.6792; 18.0812; 9.4616
90; 90.23; 90		3195.56Xiao, Bin; Schlenz, Hartmut; Bosbach, Dirk; Suleimanov, Evgeny V.; Alekseev, Evgeny V.
The structural effects of alkaline- and rare-earth element incorporation into thorium molybdates
CrystEngComm, 2016, 18, 113
7223246 CIFC20 H19 Cd N3 O6P b c a13.3916; 12.6857; 23.5448
90; 90; 90		3999.83Bhattacharya, Biswajit; Halder, Arijit; Maity, Dilip Kumar; Ghoshal, Debajyoti
Dynamic metal‒organic frameworks: syntheses, characterizations, sorption studies and their hydrolytic inter-conversion
CrystEngComm, 2016, 18, 4074
7223247 CIFC13 H10 Cd N2 O6C 1 2/c 122.4577; 11.3406; 12.0773
90; 113.556; 90		2819.6Bhattacharya, Biswajit; Halder, Arijit; Maity, Dilip Kumar; Ghoshal, Debajyoti
Dynamic metal‒organic frameworks: syntheses, characterizations, sorption studies and their hydrolytic inter-conversion
CrystEngComm, 2016, 18, 4074
7223248 CIFC26 H16 N4 O8 ZnP 1 21/c 119.13; 26.34; 11.628
90; 90.671; 90		5859Gong, Le Le; Feng, Xue Feng; Luo, Feng; Yi, Xian Feng; Zheng, An Min
Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal‒organic framework
Green Chem., 2016, 18, 2047
7223249 CIFC36 H28 N4 P2P -18.8542; 12.9976; 14.0901
100.076; 90.969; 92.406		1594.63Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223250 CIFC40 H34 F6 N4 O6 P2 S2P -114.0858; 14.4866; 15.7112
67.615; 78.55; 62.44		2627Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223251 CIFC38 H33 Cl2 I N4 P2P 1 21/c 19.5438; 39.836; 10.6814
90; 116.464; 90		3635.4Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223263 CIFC53 H110 N12 Ni2 O29C 1 2/c 137.526; 8.8468; 29.72
90; 127.61; 90		7816Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223264 CIFC57 H110 N12 Ni2 O29C 1 2/c 137.153; 8.9381; 29.414
90; 127.964; 90		7700.8Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223265 CIFC61 H120 N12 Ni2 O30C 1 2/c 137.352; 8.834; 29.562
90; 126.838; 90		7806.9Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223266 CIFC69 H124 N16 Ni2 O26P n n a11.579; 25.062; 31.421
90; 90; 90		9118Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223267 CIFC71 H126 N16 Ni2 O25P n n a11.7659; 25.7333; 31.1417
90; 90; 90		9428.9Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223268 CIFC61 H124 N12 Ni2 O32P n n a11.817; 24.76; 32.256
90; 90; 90		9438Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223269 CIFC63 H124 N12 Ni2 O30P n n a12.0122; 25.023; 31.873
90; 90; 90		9580.4Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223270 CIFC65 H108 N12 Ni2 O16I 41/a18.7966; 18.7966; 21.2715
90; 90; 90		7515.5Jiang, Xiang; Hu, Kong-Qiu; Kou, Hui-Zhong
Tunable gas adsorption properties of porous coordination polymers by modification of macrocyclic metallic tectons
CrystEngComm, 2016, 18, 4084
7223280 CIFC13 H9 F2 N OP 1 21/n 15.4223; 7.6977; 25.4353
90; 92.75; 90		1060.43Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223281 CIFC13 H9 F2 N OP n a 219.914; 21.812; 4.923
90; 90; 90		1064.6Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223282 CIFC13 H9 F2 N OP -15.4385; 7.5939; 12.8178
106.251; 100.337; 90.203		499.16Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223283 CIFC13 H9 F2 N OP -15.13; 8.8893; 11.6782
101.426; 97.174; 90.881		517.47Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223284 CIFC13 H7 F4 N OP 21 21 215.0295; 8.838; 24.4547
90; 90; 90		1087.03Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223285 CIFC13 H7 F4 N OP 1 21/n 19.456; 4.7786; 24.253
90; 95.145; 90		1091.5Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223286 CIFC13 H7 F4 N OP -14.9918; 9.361; 12.0172
102.372; 97.44; 90.222		543.59Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223287 CIFC13 H7 F4 N OP 14.6457; 5.0544; 11.8597
100.967; 92.076; 92.987		272.72Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223288 CIFC13 H9 F2 N OP 1 n 15.535; 5.035; 19.29
90; 92.048; 90		537.2Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223289 CIFC13 H7 F4 N OP 1 21/n 18.8818; 4.9233; 24.9499
90; 94.162; 90		1088.13Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223290 CIFC13 H9 F2 N OP c a 2124.3084; 5.0243; 8.4598
90; 90; 90		1033.22Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223291 CIFC13 H9 F2 N OP -15.4838; 7.7928; 12.6887
106.682; 98.87; 90.157		512.57Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223292 CIFC13 H7 F4 N OP 1 21/n 15.1818; 8.312; 25.739
90; 93.172; 90		1106.9Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223293 CIFC13 H7 F4 N OP 1 21/n 14.9514; 8.6873; 25.517
90; 91.829; 90		1097.04Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223294 CIFC13 H9 F2 N OP 1 21/n 110.179; 5.15; 20.053
90; 103.924; 90		1020.3Mondal, Pradip Kumar; Chopra, Deepak
Crystal structure landscape of conformationally flexible organo-fluorine compounds
CrystEngComm, 2016, 18, 48
7223305 CIFC64 H76 N28 O20 Zn4P 42/n13.836; 13.836; 19.957
90; 90; 90		3820.5Mahmoudi, Ghodrat; Bauzá, Antonio; Rodríguez-Diéguez, Antonio; Garczarek, Piotr; Kaminsky, Werner; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis studies of carbohydrazone based on Zn(ii) complexes
CrystEngComm, 2016, 18, 102
7223306 CIFC66 H64 Cl4 N24 O22 Zn4P 1 21/n 113.7479; 13.6207; 44.742
90; 98.226; 90		8292Mahmoudi, Ghodrat; Bauzá, Antonio; Rodríguez-Diéguez, Antonio; Garczarek, Piotr; Kaminsky, Werner; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis studies of carbohydrazone based on Zn(ii) complexes
CrystEngComm, 2016, 18, 102
7223307 CIFC64 H60 N30 O10 S4 Zn5P 1 21/n 113.39; 29.716; 21.716
90; 102.996; 90		8419.4Mahmoudi, Ghodrat; Bauzá, Antonio; Rodríguez-Diéguez, Antonio; Garczarek, Piotr; Kaminsky, Werner; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis studies of carbohydrazone based on Zn(ii) complexes
CrystEngComm, 2016, 18, 102
7223308 CIFC21 H26 N10 O3 S4 ZnP -111.452; 12.106; 13.138
115.338; 99.128; 104.707		1516.01Mahmoudi, Ghodrat; Bauzá, Antonio; Rodríguez-Diéguez, Antonio; Garczarek, Piotr; Kaminsky, Werner; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis studies of carbohydrazone based on Zn(ii) complexes
CrystEngComm, 2016, 18, 102
7223309 CIFC60 H60 N30 Na O16 Zn4I 41/a :213.9941; 13.9941; 35.739
90; 90; 90		6998.9Mahmoudi, Ghodrat; Bauzá, Antonio; Rodríguez-Diéguez, Antonio; Garczarek, Piotr; Kaminsky, Werner; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis studies of carbohydrazone based on Zn(ii) complexes
CrystEngComm, 2016, 18, 102
7223319 CIFC46 H68 N2 S2P -15.5193; 8.7116; 23.1468
84.894; 88.701; 72.509		1057.26Chen, Jianhua; Xiao, Manjun; Duan, Linrui; Wang, Qiong; Tan, Hua; Su, Ning; Liu, Yu; Yang, Renqiang; Zhu, Weiguo
Benzodi(pyridothiophene): a novel acceptor unit for application in A1-A-A1 type photovoltaic small molecules.
Physical chemistry chemical physics : PCCP, 2016, 18, 1507-1515
7223326 CIFC18 H12 Ag4 Mo12 N14 Na O40 PP 1 21/c 114.442; 22.524; 21.414
90; 129.598; 90		5367Sha, Jing-Quan; Sun, Long-Jiang; Zhu, Pei-Pei; Jiang, Jianzhuang
The first two-fold interpenetrating polyoxometalate-based coordination polymer with helical channels: structure and catalytic activities
CrystEngComm, 2016, 18, 283
7223327 CIFC58 H68 Cu2 N6 O18 P2P -111.543; 11.603; 12.615
69.352; 63.37; 78.518		1411.6Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223328 CIFC56 H56 Cu2 N6 O14 P2P 1 21/c 111.129; 14.638; 16.334
90; 90.251; 90		2660.9Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223329 CIFC37 H36 Cu N5 O8 PP -111.461; 12.537; 14.271
111.461; 111.204; 92.332		1743.4Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223330 CIFC20 H16 Cu N6 O7P -17.2609; 9.9595; 15.0827
73.778; 87.9; 89.707		1046.56Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223331 CIFC17 H17 O3 PC 1 2/c 131.662; 8.649; 11.434
90; 102.53; 90		3057Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223332 CIFC58 H68 Cu2 N6 O18 P2P -111.3974; 11.5337; 12.5848
117.067; 101.07; 101.147		1369.1Narang, Shikha; Singh, Udai P.; Venugopalan, P.
Solvent-mediated supramolecular templated assembly of a metal organophosphonate via a crystal‒amorphous‒crystal transformation
CrystEngComm, 2016, 18, 54
7223333 CIFC19 H12 F2 N O3P 1 21/n 15.8102; 23.9645; 10.9985
90; 98.602; 90		1514.19Fan, Guoling; Yang, Xiaogang; Liang, Ruizheng; Zhao, Jingwen; Li, Shuzhen; Yan, Dongpeng
Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties
CrystEngComm, 2016, 18, 240
7223334 CIFC36 H24 Cl2 N2 O6P 1 21/c 14.6752; 16.257; 19.332
90; 92.278; 90		1468.2Fan, Guoling; Yang, Xiaogang; Liang, Ruizheng; Zhao, Jingwen; Li, Shuzhen; Yan, Dongpeng
Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties
CrystEngComm, 2016, 18, 240
7223335 CIFC36 H22 Br2 F4 N2 O2P 1 21/n 15.7528; 22.874; 11.463
90; 97.874; 90		1494.2Fan, Guoling; Yang, Xiaogang; Liang, Ruizheng; Zhao, Jingwen; Li, Shuzhen; Yan, Dongpeng
Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties
CrystEngComm, 2016, 18, 240
7223336 CIFC36 H28 N2 O4P c a 2121.3375; 5.7007; 23.102
90; 90; 90		2810.1Fan, Guoling; Yang, Xiaogang; Liang, Ruizheng; Zhao, Jingwen; Li, Shuzhen; Yan, Dongpeng
Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties
CrystEngComm, 2016, 18, 240
7223337 CIFC39 H11 Br4 F16 N OP -17.8092; 12.7602; 19.323
97.533; 92.737; 107.448		1813.3Fan, Guoling; Yang, Xiaogang; Liang, Ruizheng; Zhao, Jingwen; Li, Shuzhen; Yan, Dongpeng
Molecular cocrystals of diphenyloxazole with tunable fluorescence, up-conversion emission and dielectric properties
CrystEngComm, 2016, 18, 240
7223338 CIFC8 H7 Ag N2P b c a12.2337; 9.5487; 13.0666
90; 90; 90		1526.4Liu, Liyang; Wen, Tian; Fu, Wen-Qiang; Liu, Min; Chen, Shumei; Zhang, Jian
Structure-dependent mechanochromism of two Ag(i) imidazolate chains
CrystEngComm, 2016, 18, 218
7223339 CIFC36 H36 Ag4 N8C 1 2/c 120.633; 20.797; 16.615
90; 91.842; 90		7126Liu, Liyang; Wen, Tian; Fu, Wen-Qiang; Liu, Min; Chen, Shumei; Zhang, Jian
Structure-dependent mechanochromism of two Ag(i) imidazolate chains
CrystEngComm, 2016, 18, 218
7223344 CIFC10 H11 Cl N2 O2P 1 21/n 17.65; 7.943; 18.15
90; 92.26; 90		1102Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223345 CIFC10 H9 N3 O4P -17.9402; 8.1717; 8.8975
70.343; 89.333; 72.343		515.42Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223346 CIFC11 H9 N2 O3P -14.9838; 9.8417; 10.3031
100.059; 100.517; 91.372		488.42Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223347 CIFC14 H12 N2 O5P -15.3961; 9.4163; 13.6395
75.67; 89.392; 80.448		661.83Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223348 CIFC13 H13 N2 O3P 1 21/n 112.7021; 5.0401; 19.1216
90; 98.951; 90		1209.25Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223349 CIFC12 H11 N2 O3P 1 21/n 112.7915; 5.0009; 16.4829
90; 90.926; 90		1054.26Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223350 CIFC12 H10 N2 O3P 1 21/n 112.6838; 5.0451; 16.3375
90; 90.201; 90		1045.45Tarai, Arup; Baruah, Jubaraj B.
Oxime synthons in the salts and cocrystals of quinoline-4-carbaldoxime for non-covalent synthesis
CrystEngComm, 2016, 18, 298
7223351 CIFC11 H17 Co N O8P -17.8758; 9.1877; 11.3427
112.883; 91.057; 105.877		720.07Chisca, Diana; Croitor, Lilia; Petuhov, Oleg; Coropceanu, Eduard B.; Fonari, Marina S.
MOF-71 as a degradation product in single crystal to single crystal transformation of new three-dimensional Co(ii) 1,4-benzenedicarboxylate
CrystEngComm, 2016, 18, 38
7223352 CIFC11 H11 Co N O5I m m a19.228; 7.24; 8.874
90; 90; 90		1235.4Chisca, Diana; Croitor, Lilia; Petuhov, Oleg; Coropceanu, Eduard B.; Fonari, Marina S.
MOF-71 as a degradation product in single crystal to single crystal transformation of new three-dimensional Co(ii) 1,4-benzenedicarboxylate
CrystEngComm, 2016, 18, 38
7223353 CIFC50 H54 F3 I3 N6 O2 S2C 1 2/c 127.3644; 13.4467; 28.0955
90; 94.042; 90		10312.3Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223354 CIFC29 H29 F3 I3 N3 O2P -110.4878; 12.3896; 12.7932
78.982; 82.201; 81.597		1604.2Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223355 CIFC28 H27 F3 I3 N3 O2P -19.5328; 11.9482; 13.9164
82.274; 85.796; 87.527		1565.57Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223356 CIFC27 H25 F3 I3 N3 O2P -19.5563; 11.4823; 14.152
99.118; 92.177; 92.289		1530.48Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223357 CIFC26 H23 F3 I3 N3 O2P -110.0662; 14.4987; 20.6364
82.22; 81.567; 89.177		2951.78Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223358 CIFC25 H21 F3 I3 N3 O2P -19.0898; 12.7927; 13.8531
114.273; 98.513; 100.445		1398.93Hidalgo, Paulina I.; Leal, Sergio; Jiménez, Claudio A.; Vöhringer-Martinez, Esteban; Herrera, Bárbara; Pasán, Jorge; Ruiz-Pérez, Catalina; Bruce, Duncan W.
Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives
CrystEngComm, 2016, 18, 42
7223359 CIFC24 H22 Cl2 Cu2 N12 O8P 1 21/c 113.1874; 11.9065; 19.8014
90; 100.142; 90		3060.6Barros, Wdeson P.; Luisa Calatayud, M.; Lloret, Francesc; Julve, Miguel; Marino, Nadia; De Munno, Giovanni; Stumpf, Humberto O.; Ruiz-García, Rafael; Castro, Isabel
Self-assembly, binding ability and magnetic properties of dicopper(ii) pyrazolenophanes
CrystEngComm, 2016, 18, 437
7223360 CIFC90 H82 Cl6 Cu6 N24 O32P n m a12.6355; 41.3258; 20.8981
90; 90; 90		10912.4Barros, Wdeson P.; Luisa Calatayud, M.; Lloret, Francesc; Julve, Miguel; Marino, Nadia; De Munno, Giovanni; Stumpf, Humberto O.; Ruiz-García, Rafael; Castro, Isabel
Self-assembly, binding ability and magnetic properties of dicopper(ii) pyrazolenophanes
CrystEngComm, 2016, 18, 437
7223361 CIFC36 H37 Cl2 Cu2 N9 O10P b c m8.497; 25.544; 18.675
90; 90; 90		4053.4Barros, Wdeson P.; Luisa Calatayud, M.; Lloret, Francesc; Julve, Miguel; Marino, Nadia; De Munno, Giovanni; Stumpf, Humberto O.; Ruiz-García, Rafael; Castro, Isabel
Self-assembly, binding ability and magnetic properties of dicopper(ii) pyrazolenophanes
CrystEngComm, 2016, 18, 437
7223362 CIFC42 H44 Cl2 Cu2 N10 O8P 1 21/c 113.841; 8.0261; 39.946
90; 96.565; 90		4408.5Barros, Wdeson P.; Luisa Calatayud, M.; Lloret, Francesc; Julve, Miguel; Marino, Nadia; De Munno, Giovanni; Stumpf, Humberto O.; Ruiz-García, Rafael; Castro, Isabel
Self-assembly, binding ability and magnetic properties of dicopper(ii) pyrazolenophanes
CrystEngComm, 2016, 18, 437
7223369 CIFC30 H30 N2 O11P 1 21 113.029; 9.107; 13.565
90; 116.569; 90		1439.6Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223370 CIFC33 H38 N2 O11C 1 2 113.604; 9.974; 13.84
90; 119.099; 90		1640.9Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223371 CIFC32 H36 N2 O12C 1 2 113.524; 9.9285; 13.891
90; 118.817; 90		1634.2Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223372 CIFC28.5 H30 N O8.5C 1 2 116.286; 22.708; 7.95
90; 115.707; 90		2649.1Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223373 CIFC40 H52 N2 O12P 21 21 217.7919; 21.208; 24.416
90; 90; 90		4034.8Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223374 CIFC33 H32 N2 O8I 4128.639; 28.639; 7.8757
90; 90; 90		6460Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223375 CIFC42 H54 N2 O11P 21 21 217.7836; 22.234; 24.89
90; 90; 90		4307.5Kodama, Koichi; Morita, Yuya; Sekine, Eriko; Hirose, Takuji
A systematic study on ternary inclusion crystals consisting of dianilines and three positional isomers of ditoluoyl-l-tartaric acid
CrystEngComm, 2016, 18, 123
7223396 CIFC6 H7 Mg1.5 O7 SP 1 21/c 16.4499; 19.1637; 8.0685
90; 96.557; 90		990.77M., Prabu; Asha, K. S.; Sinha, Mekhola; Poduval, Anamika; Mandal, Sukhendu
The structural diversity, band gap energy and photoluminescence properties of thiophenedicarboxylate based coordination polymers
CrystEngComm, 2016, 18, 536
7223397 CIFC14 H4 Mg1.5 N O8 S2P -19.6615; 10.49; 11.9404
110.295; 91.875; 114.86		1006.93M., Prabu; Asha, K. S.; Sinha, Mekhola; Poduval, Anamika; Mandal, Sukhendu
The structural diversity, band gap energy and photoluminescence properties of thiophenedicarboxylate based coordination polymers
CrystEngComm, 2016, 18, 536
7223398 CIFC27 H16 N3 O8.5 S2 Zn2C 1 2/c 134.681; 15.3678; 13.7141
90; 112.169; 90		6768.9M., Prabu; Asha, K. S.; Sinha, Mekhola; Poduval, Anamika; Mandal, Sukhendu
The structural diversity, band gap energy and photoluminescence properties of thiophenedicarboxylate based coordination polymers
CrystEngComm, 2016, 18, 536
7223399 CIFC18 H18 Mg2 N2 O10 S2P 1 21/n 110.0483; 13.4969; 16.7346
90; 93.683; 90		2264.87M., Prabu; Asha, K. S.; Sinha, Mekhola; Poduval, Anamika; Mandal, Sukhendu
The structural diversity, band gap energy and photoluminescence properties of thiophenedicarboxylate based coordination polymers
CrystEngComm, 2016, 18, 536
7223400 CIFC7 H2 In0.5 N0.5 O4 SP 43 2 213.5642; 13.5642; 15.6425
90; 90; 90		2878M., Prabu; Asha, K. S.; Sinha, Mekhola; Poduval, Anamika; Mandal, Sukhendu
The structural diversity, band gap energy and photoluminescence properties of thiophenedicarboxylate based coordination polymers
CrystEngComm, 2016, 18, 536
7223403 CIFC39 H72 Br12 N6 S4 ZnP 1 21 113.6976; 16.1004; 14.1055
90; 92.642; 90		3107.5Rosokha, Sergiy V.; Stern, Charlotte L.; Vinakos, Michael K.
From single-point to three-point halogen bonding between zinc(ii) tetrathiocyanate and tetrabromomethane
CrystEngComm, 2016, 18, 488
7223404 CIFC114 H124 Gd2 N2 O47 P2 S8P n n n12.3714; 13.3655; 37.5272
90; 90; 90		6205.1Ling, Irene; Sobolev, Alexandre N.; Raston, Colin L.
Gadolinium(iii)-mediated multi-component confinement of imidazolium cations in p-sulfonated calix[4]arene
CrystEngComm, 2016, 18, 4929
7223405 CIFC167 H195 N2 O60 P4 S8P -117.4699; 18.0265; 23.3461
102.788; 96.123; 118.576		6099.4Ling, Irene; Sobolev, Alexandre N.; Raston, Colin L.
Gadolinium(iii)-mediated multi-component confinement of imidazolium cations in p-sulfonated calix[4]arene
CrystEngComm, 2016, 18, 4929
7223406 CIFC25 H22 I O PP -110.4708; 10.5478; 11.0342
72.783; 75.786; 70.243		1081.09Ling, Irene; Sobolev, Alexandre N.; Raston, Colin L.
Gadolinium(iii)-mediated multi-component confinement of imidazolium cations in p-sulfonated calix[4]arene
CrystEngComm, 2016, 18, 4929
7223407 CIFC7 H15 Cl5 Co N2P n m a11.178; 10.166; 12.216
90; 90; 90		1388Chen, Chun-Hong; Xu, Guan-Cheng
Synthesis, characterization and disorder‒order phase transition of inorganic‒organic hybrid materials (H2dabco-CH2-Cl)[MIICl4] (M = Co, Zn)
CrystEngComm, 2016, 18, 550
7223408 CIFC7 H15 Cl5 Co N2P 1 21/c 110.0525; 12.081; 11.042
90; 91.329; 90		1340.6Chen, Chun-Hong; Xu, Guan-Cheng
Synthesis, characterization and disorder‒order phase transition of inorganic‒organic hybrid materials (H2dabco-CH2-Cl)[MIICl4] (M = Co, Zn)
CrystEngComm, 2016, 18, 550
7223409 CIFC7 H15 Cl5 N2 ZnP n m a11.19; 10.204; 12.278
90; 90; 90		1401.9Chen, Chun-Hong; Xu, Guan-Cheng
Synthesis, characterization and disorder‒order phase transition of inorganic‒organic hybrid materials (H2dabco-CH2-Cl)[MIICl4] (M = Co, Zn)
CrystEngComm, 2016, 18, 550
7223410 CIFC7 H15 Cl5 N2 ZnP 1 21/c 110.0664; 12.075; 11.0158
90; 91.262; 90		1338.7Chen, Chun-Hong; Xu, Guan-Cheng
Synthesis, characterization and disorder‒order phase transition of inorganic‒organic hybrid materials (H2dabco-CH2-Cl)[MIICl4] (M = Co, Zn)
CrystEngComm, 2016, 18, 550
7223426 CIFC16 H21 Br O SiP 1 21 17.0513; 7.6501; 15.5178
90; 101.367; 90		820.66Beckmann, Peter A.; Moore, Curtis E.; Rheingold, Arnold L.
Methyl and t-butyl group rotation in a molecular solid: (1)H NMR spin-lattice relaxation and X-ray diffraction.
Physical chemistry chemical physics : PCCP, 2016, 18, 1720-1726
7223436 CIFC18 H32 Ni2 O18P n a 2115.4414; 10.9156; 14.596
90; 90; 90		2460.2McCormick, Laura J.; Morris, Samuel A.; Slawin, Alexandra M. Z.; Teat, Simon J.; Morris, Russell E.
Coordination polymers of 5-substituted isophthalic acid.
CrystEngComm / RSC, 2016, 18, 1123-1132
7223437 CIFC45 H54.75 O33.5 Zn6P n n 220.775; 27.566; 10.846
90; 90; 90		6211.3McCormick, Laura J.; Morris, Samuel A.; Slawin, Alexandra M. Z.; Teat, Simon J.; Morris, Russell E.
Coordination polymers of 5-substituted isophthalic acid.
CrystEngComm / RSC, 2016, 18, 1123-1132
7223438 CIFC45 H44 O28 Zn6P 21 21 217.382; 10.4516; 15.97
90; 90; 90		2901.3McCormick, Laura J.; Morris, Samuel A.; Slawin, Alexandra M. Z.; Teat, Simon J.; Morris, Russell E.
Coordination polymers of 5-substituted isophthalic acid.
CrystEngComm / RSC, 2016, 18, 1123-1132
7223439 CIFC18 H14 Mn O10P 1 21/c 14.5131; 14.483; 12.622
90; 97.792; 90		817.4McCormick, Laura J.; Morris, Samuel A.; Slawin, Alexandra M. Z.; Teat, Simon J.; Morris, Russell E.
Coordination polymers of 5-substituted isophthalic acid.
CrystEngComm / RSC, 2016, 18, 1123-1132
7223440 CIFC52 H62 Mn3 O18P -19.1496; 9.7908; 16.078
89.207; 76.087; 74.643		1346.2McCormick, Laura J.; Morris, Samuel A.; Slawin, Alexandra M. Z.; Teat, Simon J.; Morris, Russell E.
Coordination polymers of 5-substituted isophthalic acid.
CrystEngComm / RSC, 2016, 18, 1123-1132
7223441 CIFC23 H26 N2 O2P 1 21/c 19.0471; 17.5709; 12.943
90; 109.25; 90		1942.5Harvey, Benjamin G.; Guenthner, Andrew J.; Koontz, Thomas A.; Storch, Perrin J.; Reams, Josiah T.; Groshens, Thomas J.
Sustainable hydrophobic thermosetting resins and polycarbonates from turpentine
Green Chem., 2016, 18, 2416
7223442 CIFC28 H24 N2 O3 SP -19.0258; 11.0099; 12.4506
79.449; 76.11; 80.803		1172Dandia, Anshu; Parewa, Vijay; Kumari, Sukhbeer; Bansal, Sarika; Sharma, Amit
Imposed hydrophobic interactions by NaCl: accountable attribute for the synthesis of spiro[acenaphthylene-1,5′-pyrrolo[1,2-c]thiazole] derivatives via 1,3-dipolar cycloaddition reaction in aqueous medium
Green Chem., 2016, 18, 2488
7223456 CIFC48 H46 As8 N18 Ni5 O43 V14P 1 2/c 114.861; 14.142; 22.798
90; 106.37; 90		4597.1Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223457 CIFC46 H41 As8 N12 Ni2.5 O43 V14P 21 21 2113.80109; 23.8678; 27.1204
90; 90; 90		8933.5Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223458 CIFC42 H36 As8 N8 Ni2 O44 V14P 21 21 2112.169; 16.057; 40.244
90; 90; 90		7864Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223459 CIFC52 H58 As8 N16 Ni2 O49 V14I 41/a15.5647; 15.5647; 38.904
90; 90; 90		9424.9Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223460 CIFC68 H58 As8 Cd2 N12 O47 V14P -111.5263; 15.2606; 15.8895
106.238; 95.372; 102.466		2584.6Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223461 CIFC50 H50 As6 Cd4 N8 O55 V15P -112.541; 12.565; 14.238
83.592; 79.184; 81.137		2169.5Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223462 CIFC60 H52 As8 Co2 N12 O49 V14P -111.6254; 14.4554; 14.651
99.363; 97.293; 91.069		2407.7Guo, Hai-Yang; Li, Zhi-Fang; Zhang, Xiao; Fu, Li-Wei; Hu, Yang-Yang; Guo, Lan-Lan; Cui, Xiao-Bing; Huo, Qi-Sheng; Xu, Ji-Qing
New self-assembly hybrid compounds based on arsenic‒vanadium clusters and transition metal mixed-organic-ligand complexes
CrystEngComm, 2016, 18, 566
7223463 CIFC13 H13 Cu2.5 N7P 1 21/c 114.4313; 13.2244; 7.5812
90; 93.883; 90		1443.51Hsu, Wayne; Thapa, Kedar Bahadur; Yang, Xiang-Kai; Chen, Kuan-Ting; Chang, Han-Yun; Chen, Jhy-Der
Dinitrogen-supported coordination polymers
CrystEngComm, 2016, 18, 390
7223464 CIFC14 H18 Cu3 N10 OP 1 21/n 17.3329; 18.6223; 14.8934
90; 101.642; 90		1991.94Hsu, Wayne; Thapa, Kedar Bahadur; Yang, Xiang-Kai; Chen, Kuan-Ting; Chang, Han-Yun; Chen, Jhy-Der
Dinitrogen-supported coordination polymers
CrystEngComm, 2016, 18, 390
7223470 CIFC12 H6 O6 ScF d d d :28.785; 20.81; 34.48
90; 90; 90		6303McKellar, Scott C.; Sotelo, Jorge; Mowat, John P. S.; Wright, Paul A.; Moggach, Stephen A.
Perfluorocarbon liquid under pressure: a medium for gas delivery
CrystEngComm, 2016, 18, 1273
7223471 CIFC12 H6 O6 ScF d d d :28.798; 20.865; 34.551
90; 90; 90		6343McKellar, Scott C.; Sotelo, Jorge; Mowat, John P. S.; Wright, Paul A.; Moggach, Stephen A.
Perfluorocarbon liquid under pressure: a medium for gas delivery
CrystEngComm, 2016, 18, 1273
7223472 CIFC12.56 H6 O7.125 ScC 1 2/c 18.7007; 34.271; 11.0753
90; 111.047; 90		3082.1McKellar, Scott C.; Sotelo, Jorge; Mowat, John P. S.; Wright, Paul A.; Moggach, Stephen A.
Perfluorocarbon liquid under pressure: a medium for gas delivery
CrystEngComm, 2016, 18, 1273
7223487 CIFC72 H48 Ag3 Fe2 I7 N12R -3 c :H15.1612; 15.1612; 58.187
90; 90; 120		11583Lei, Xiao-Wu; Yue, Cheng-Yang; Feng, Li-Juan; Han, Yong-Fang; Meng, Rong-Rong; Yang, Jiang-Tao; Ding, Hao; Gao, Chuan-Sheng; Wang, Chun-Yan
Syntheses, crystal structures and photocatalytic properties of four hybrid iodoargentates with zero- and two-dimensional structures
CrystEngComm, 2016, 18, 427
7223488 CIFC72 H48 Ag3 I7 Mn2 N12R -3 c :H15.1789; 15.1789; 58.192
90; 90; 120		11611.1Lei, Xiao-Wu; Yue, Cheng-Yang; Feng, Li-Juan; Han, Yong-Fang; Meng, Rong-Rong; Yang, Jiang-Tao; Ding, Hao; Gao, Chuan-Sheng; Wang, Chun-Yan
Syntheses, crystal structures and photocatalytic properties of four hybrid iodoargentates with zero- and two-dimensional structures
CrystEngComm, 2016, 18, 427
7223489 CIFC36 H24 Ag5 I7 Mn N6P -114.7523; 14.7794; 27.291
76.78; 86.843; 60.318		5020.6Lei, Xiao-Wu; Yue, Cheng-Yang; Feng, Li-Juan; Han, Yong-Fang; Meng, Rong-Rong; Yang, Jiang-Tao; Ding, Hao; Gao, Chuan-Sheng; Wang, Chun-Yan
Syntheses, crystal structures and photocatalytic properties of four hybrid iodoargentates with zero- and two-dimensional structures
CrystEngComm, 2016, 18, 427
7223490 CIFC48 H56 Ag14 I22 N8P -111.396; 18.948; 23.015
100.441; 94.951; 100.227		4773.5Lei, Xiao-Wu; Yue, Cheng-Yang; Feng, Li-Juan; Han, Yong-Fang; Meng, Rong-Rong; Yang, Jiang-Tao; Ding, Hao; Gao, Chuan-Sheng; Wang, Chun-Yan
Syntheses, crystal structures and photocatalytic properties of four hybrid iodoargentates with zero- and two-dimensional structures
CrystEngComm, 2016, 18, 427
7223491 CIFCu6 Mo28 N2 O96I 4/m17.2929; 17.2929; 19.8829
90; 90; 90		5945.9Zhao, Yifang; Yuan, Youyou; Du, Xin; Lin, Xiaohuan; Liao, Fuhui; Xie, Jinglin; Lin, Jianhua; Sun, Junliang
Hydrothermal assembly of various dimensional pure-inorganic copper‒molybdenum frameworks
CrystEngComm, 2016, 18, 521
7223492 CIFCu Mo7 O24P -110.3503; 10.3933; 15.1733
76.113; 75.04; 62.687		1387Zhao, Yifang; Yuan, Youyou; Du, Xin; Lin, Xiaohuan; Liao, Fuhui; Xie, Jinglin; Lin, Jianhua; Sun, Junliang
Hydrothermal assembly of various dimensional pure-inorganic copper‒molybdenum frameworks
CrystEngComm, 2016, 18, 521
7223493 CIFCu Mo7 O24P n m a10.4495; 19.2758; 13.2417
90; 90; 90		2667.2Zhao, Yifang; Yuan, Youyou; Du, Xin; Lin, Xiaohuan; Liao, Fuhui; Xie, Jinglin; Lin, Jianhua; Sun, Junliang
Hydrothermal assembly of various dimensional pure-inorganic copper‒molybdenum frameworks
CrystEngComm, 2016, 18, 521
7223504 CIFC98 H79 N5 O28 Zn6C 1 2/c 119.953; 9.495; 25.805
90; 91.915; 90		4886Zhang, Chuanqi; Yan, Yan; Sun, Libo; Liang, Zhiqiang; Li, Jiyang
Solvent-induced construction of two zinc metal‒organic frameworks for highly selective detection of nitroaromatic explosives
CrystEngComm, 2016, 18, 4102
7223505 CIFC26 H26 N2 O7 ZnP b c n16.7153; 8.4558; 35.4943
90; 90; 90		5016.8Zhang, Chuanqi; Yan, Yan; Sun, Libo; Liang, Zhiqiang; Li, Jiyang
Solvent-induced construction of two zinc metal‒organic frameworks for highly selective detection of nitroaromatic explosives
CrystEngComm, 2016, 18, 4102
7223506 CIFC174 H170 Br8 Cl4 Dy4 N18 Ni4 O52P -113.4199; 19.4201; 20.7033
88.22; 85.02; 84.859		5352.1Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223507 CIFC82 H92 N4 Ni4 O22P -118.0377; 18.3422; 29.9
71.347; 71.67; 67.774		8462.6Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223508 CIFC92 H112 Cl2 Dy2 N4 Ni2 O30P 1 21/n 112.1956; 19.3817; 20.2019
90; 98.464; 90		4723.1Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223509 CIFC106 H122 Cl2 Dy2 N10 Ni2 O28P 1 21/c 115.0768; 20.6499; 17.8256
90; 103.01; 90		5407.3Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223510 CIFC62 H58 Dy2 N4 Ni2 O18P 1 21/c 110.4776; 21.3408; 14.3681
90; 106.977; 90		3072.7Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223511 CIFC88 H76 Co2 Dy2 N14 O34P -113.149; 13.62; 15.4701
68.869; 65.65; 63.614		2207.1Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223512 CIFC94 H90 Co2 Dy2 N14 O32P -112.7821; 13.5743; 14.1583
106.94; 91.065; 97.754		2324.2Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223513 CIFC81 H69 Dy3 N24 O60P -116.5657; 17.6842; 18.4698
81.572; 80.148; 83.02		5247.5Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223514 CIFC181 H171 Dy4 N27 Ni4 O66P -114.1586; 17.259; 22.3936
98.527; 98.268; 111.403		4920.7Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223515 CIFC14 H11 Cl N2 O5P -16.9697; 12.6645; 15.0866
76.153; 89.966; 88.423		1292.45Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223516 CIFC21 H20 Br N O4P -17.5662; 8.5456; 14.8304
84.747; 84.775; 82.09		942.79Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223517 CIFC36 H44 Co N5 O12P 1 21/c 118.8624; 17.03; 25.6461
90; 108.353; 90		7819.2Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223518 CIFC45 H52 Br2 Co N3 O9P 1 21/n 113.059; 22.7258; 15.4472
90; 109.616; 90		4318.3Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223519 CIFC120.5 H115 Cl5 Dy2 N4 Ni2 O20C 1 2/c 122.1776; 18.894; 27.8333
90; 100.127; 90		11481.1Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223520 CIFC122 H146 Cl2 Dy2 N14 Ni2 O30P -112.5403; 14.7915; 18.88
100.291; 106.198; 105.143		3124.5Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223521 CIFC112 H114 Br6 Dy2 N4 Ni2 O26C 1 2/c 120.462; 20.8069; 27.3553
90; 98.444; 90		11520.3Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223522 CIFC122 H130 Dy2 N4 Ni2 O24R -338.159; 38.159; 18.7654
90; 90; 120		23664Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223523 CIFC102 H110 Cl2 Dy2 N10 Ni2 O26P 1 21/n 115.8855; 17.2105; 20.5903
90; 96.747; 90		5590.3Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223524 CIFC64 H72 Cl2 Dy2 N4 Ni2 O26P 1 21/n 112.1724; 14.1352; 19.123
90; 99.425; 90		3245.9Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223525 CIFC82 H100 Dy2 F6 N12 Ni2 O26 S2P 1 21/c 116.6632; 18.8674; 15.7017
90; 109.993; 90		4638.98Griffiths, Kieran; Dokorou, Vassiliki N.; Spencer, John; Abdul-Sada, Alaa; Vargas, Alfredo; Kostakis, George E.
Isoskeletal Schiff base polynuclear coordination clusters: synthetic and theoretical aspects
CrystEngComm, 2016, 18, 704
7223526 CIFC42 H30 Co3 N6 O12 S3P -110.947; 11.0433; 17.924
99.305; 96.75; 90.261		2122.9Chisca, Diana; Croitor, Lilia; Coropceanu, Eduard B.; Petuhov, Oleg; Baca, Svetlana G.; Krämer, Karl; Liu, Shi-Xia; Decurtins, Silvio; Rivera-Jacquez, Hector J.; Masunov, Artëm E.; Fonari, Marina S.
From pink to blue and back to pink again: changing the Co(ii) ligation in a two-dimensional coordination network upon desolvation
CrystEngComm, 2016, 18, 384
7223527 CIFC37 H47 Co2 N7 O14 S2P -110.6132; 13.4256; 17.8366
78.86; 76.42; 72.302		2333.1Chisca, Diana; Croitor, Lilia; Coropceanu, Eduard B.; Petuhov, Oleg; Baca, Svetlana G.; Krämer, Karl; Liu, Shi-Xia; Decurtins, Silvio; Rivera-Jacquez, Hector J.; Masunov, Artëm E.; Fonari, Marina S.
From pink to blue and back to pink again: changing the Co(ii) ligation in a two-dimensional coordination network upon desolvation
CrystEngComm, 2016, 18, 384
7223528 CIFC37 H47 Co2 N7 O14 S2P -110.5028; 13.3758; 17.9703
78.0998; 75.4371; 71.7708		2298.34Chisca, Diana; Croitor, Lilia; Coropceanu, Eduard B.; Petuhov, Oleg; Baca, Svetlana G.; Krämer, Karl; Liu, Shi-Xia; Decurtins, Silvio; Rivera-Jacquez, Hector J.; Masunov, Artëm E.; Fonari, Marina S.
From pink to blue and back to pink again: changing the Co(ii) ligation in a two-dimensional coordination network upon desolvation
CrystEngComm, 2016, 18, 384
7223529 CIFC92 H168 Cu12 Mo N5 O130 Si W11F m -3 m26.232; 26.232; 26.232
90; 90; 90		18051Li, Chong; Sun, Minghui; Xu, Lin; Wang, Yuchao; Huang, Jiawei
The first heteropoly blue-embedded metal‒organic framework: crystal structure, magnetic property and proton conductivity
CrystEngComm, 2016, 18, 596
7223530 CIFC47 H39 NP n m a15.6323; 14.7468; 14.4198
90; 90; 90		3324.1Kuck, Dietmar; Linke, Jens; Teichmann, Lisa Christin; Barth, Dieter; Tellenbröker, Jörg; Gestmann, Detlef; Neumann, Beate; Stammler, Hans-Georg; Bögge, Hartmut
Centrohexaindane: six benzene rings mutually fixed in three dimensions - solid-state structure and six-fold nitration.
Physical chemistry chemical physics : PCCP, 2016, 18, 11722-11737
7223531 CIFC42 H25 Cl3P -18.51239; 12.4653; 14.2625
91.3139; 93.6817; 101.235		1480.35Kuck, Dietmar; Linke, Jens; Teichmann, Lisa Christin; Barth, Dieter; Tellenbröker, Jörg; Gestmann, Detlef; Neumann, Beate; Stammler, Hans-Georg; Bögge, Hartmut
Centrohexaindane: six benzene rings mutually fixed in three dimensions - solid-state structure and six-fold nitration.
Physical chemistry chemical physics : PCCP, 2016, 18, 11722-11737
7223532 CIFC45 H29P 1 21/c 18.42; 14.384; 24.107
90; 91.53; 90		2918.64Kuck, Dietmar; Linke, Jens; Teichmann, Lisa Christin; Barth, Dieter; Tellenbröker, Jörg; Gestmann, Detlef; Neumann, Beate; Stammler, Hans-Georg; Bögge, Hartmut
Centrohexaindane: six benzene rings mutually fixed in three dimensions - solid-state structure and six-fold nitration.
Physical chemistry chemical physics : PCCP, 2016, 18, 11722-11737
7223540 CIFC15 H24 N4 O13.5 SmP -19.1586; 9.5032; 13.9208
95.383; 91.851; 107.7		1146.8Xiao, Yu; Wang, Shuai-Hua; Zheng, Fa-Kun; Wu, Mei-Feng; Xu, Ju; Liu, Zhi-Fa; Chen, Jun; Li, Rong; Guo, Guo-Cong
Excitation wavelength-induced color-tunable and white-light emissions in lanthanide(iii) coordination polymers constructed using an environment-dependent luminescent tetrazolate‒dicarboxylate ligand
CrystEngComm, 2016, 18, 721
7223541 CIFC15 H24 Eu N4 O13.5P -19.1406; 9.4909; 13.9426
95.29; 91.86; 107.708		1145Xiao, Yu; Wang, Shuai-Hua; Zheng, Fa-Kun; Wu, Mei-Feng; Xu, Ju; Liu, Zhi-Fa; Chen, Jun; Li, Rong; Guo, Guo-Cong
Excitation wavelength-induced color-tunable and white-light emissions in lanthanide(iii) coordination polymers constructed using an environment-dependent luminescent tetrazolate‒dicarboxylate ligand
CrystEngComm, 2016, 18, 721
7223542 CIFC15 H24 Gd N4 O13.5P -19.0892; 9.4506; 13.922
95.202; 91.845; 107.559		1133.23Xiao, Yu; Wang, Shuai-Hua; Zheng, Fa-Kun; Wu, Mei-Feng; Xu, Ju; Liu, Zhi-Fa; Chen, Jun; Li, Rong; Guo, Guo-Cong
Excitation wavelength-induced color-tunable and white-light emissions in lanthanide(iii) coordination polymers constructed using an environment-dependent luminescent tetrazolate‒dicarboxylate ligand
CrystEngComm, 2016, 18, 721
7223543 CIFC15 H24 Eu0.12 Gd0.88 N4 O13.5P -19.117; 9.474; 13.956
95.423; 91.643; 107.538		1142.2Xiao, Yu; Wang, Shuai-Hua; Zheng, Fa-Kun; Wu, Mei-Feng; Xu, Ju; Liu, Zhi-Fa; Chen, Jun; Li, Rong; Guo, Guo-Cong
Excitation wavelength-induced color-tunable and white-light emissions in lanthanide(iii) coordination polymers constructed using an environment-dependent luminescent tetrazolate‒dicarboxylate ligand
CrystEngComm, 2016, 18, 721
7223544 CIFC54 H36 N4 O13 ZnP -111.8801; 13.7323; 13.9872
84.567; 79.104; 79.225		2197.1Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223545 CIFC42 H30 Co N8 O12P -18.0674; 9.264; 13.4563
72.758; 83.095; 82.579		948.9Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223546 CIFC42 H30 Cd N8 O12P -18.0767; 9.4789; 13.3988
73.886; 83.844; 80.81		970.69Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223547 CIFC39 H30 N4 Ni O9P n a 2114.4; 13.9197; 17.1576
90; 90; 90		3439.1Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223548 CIFC39 H23 Cd2 Cl N4 O6P c a 2120.3729; 9.7388; 17.7787
90; 90; 90		3527.43Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223549 CIFC49 H42 N4 Ni3 O16C 1 2/c 120.505; 10.3482; 29.521
90; 113.518; 90		5743.7Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223550 CIFC60 H52 Co3 N6 O16C 1 2/c 120.6; 10.4271; 29.646
90; 113.51; 90		5839Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223551 CIFC40 H33 Co3.5 N2 O17P -112.058; 12.3182; 15.3976
67.945; 88.887; 80.778		2090.2Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223552 CIFC30 H18 O14 Pb3P 1 21/n 113.48481; 12.1638; 17.6457
90; 95.1954; 90		2882.47Shao, Yong-Liang; Cui, Yan-Hui; Gu, Jin-Zhong; Wu, Jiang; Wang, Ya-Wen; Kirillov, Alexander M.
Exploring biphenyl-2,4,4′-tricarboxylic acid as a flexible building block for the hydrothermal self-assembly of diverse metal‒organic and supramolecular networks
CrystEngComm, 2016, 18, 765
7223553 CIFC84 H72 N8 O19 S24P 1 21/m 110.8302; 33.4895; 13.8319
90; 99.191; 90		4952.4Xue, Li-Jun; Huo, Peng; Li, Yan-Hong; Hou, Jin-Le; Zhu, Qin-Yu; Dai, Jie
An ionic charge-transfer dyad prepared cost-effectively from a tetrathiafulvalene carboxylate anion and a TMPyP cation.
Physical chemistry chemical physics : PCCP, 2016, 18, 2940-2948
7223554 CIFC64 H52 N8 O21 S8C 1 2/c 123.6681; 22.0587; 13.2272
90; 111.589; 90		6421.3Xue, Li-Jun; Huo, Peng; Li, Yan-Hong; Hou, Jin-Le; Zhu, Qin-Yu; Dai, Jie
An ionic charge-transfer dyad prepared cost-effectively from a tetrathiafulvalene carboxylate anion and a TMPyP cation.
Physical chemistry chemical physics : PCCP, 2016, 18, 2940-2948
7223579 CIFC60 H74 N8 O5 S4P 1 21/c 115.2164; 13.1809; 29.309
90; 92.577; 90		5872.4Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223580 CIFC60 H72 N8 S8C 1 2/c 126.6378; 12.7707; 19.6019
90; 115.002; 90		6043.4Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223581 CIFC143 H187 Ag4 Cl21 F24 N16 O2 S16 Sb4P -118.8461; 19.0515; 19.1473
99.994; 113.12; 115.126		5224.5Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223582 CIFC34 H46 Ag N5 O4 S4C 1 2/c 136.0428; 12.4438; 20.2117
90; 121.056; 90		7765.8Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223583 CIFC66 H82 Ag2 Cl6 F12 N8 S8 Sb2P -115.6888; 17.4322; 17.6605
80.598; 76.588; 71.025		4422.6Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223584 CIFC30 H42 Ag F6 N4 O3 S4 SbI -4 2 d24.958; 24.958; 13.8496
90; 90; 90		8626.9Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223585 CIFC30 H42 Ag F6 N4 O3 P S4I -4 2 d24.2538; 24.2538; 13.6809
90; 90; 90		8047.7Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223586 CIFC60 H74 Ag2 B2 F8 N8 O S8I 41/a16.0983; 16.0983; 54.7728
90; 90; 90		14194.7Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223587 CIFC30 H42 Ag As F6 N4 O3 S4I -4 2 d24.4165; 24.4165; 13.7457
90; 90; 90		8194.7Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223588 CIFC69 H89 Ag Cl3 F6 N8 O4 S4 SbP 1 21/c 116.8948; 14.6737; 30.1055
90; 90.706; 90		7462.9Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223589 CIFC68 H94 Ag B F4 N8 O7 S4C 1 c 122.7969; 17.2741; 19.4952
90; 103.786; 90		7456Ovsyannikov, A. S.; Noamane, M. H.; Abidi, R.; Ferlay, S.; Solovieva, S. E.; Antipin, I. S.; Konovalov, A. I.; Kyritsakas, N.; Hosseini, M. W.
Molecular tectonics: dimensionality and geometry control of silver coordination networks based on pyrazolyl appended thiacalixarenes
CrystEngComm, 2016, 18, 691
7223590 CIFC110 H140 Ag3 F18 N12 O12 P3P 1 21/c 134.813; 20.6402; 16.304
90; 102.678; 90		11429.6Tominaga, Masahide; Kawaguchi, Taichi; Ohara, Kazuaki; Yamaguchi, Kentaro; Masu, Hyuma; Azumaya, Isao
Synthesis and crystal structures of twisted three-dimensional assemblies of adamantane-bridged tris-NHC ligands and AgI
CrystEngComm, 2016, 18, 266
7223591 CIFC16 H16 Ag0.4 F2.4 N1.73 O0.53 P0.4P 1 21/c 119.0224; 15.7764; 38.4287
90; 102.187; 90		11272.7Tominaga, Masahide; Kawaguchi, Taichi; Ohara, Kazuaki; Yamaguchi, Kentaro; Masu, Hyuma; Azumaya, Isao
Synthesis and crystal structures of twisted three-dimensional assemblies of adamantane-bridged tris-NHC ligands and AgI
CrystEngComm, 2016, 18, 266
7223596 CIFC8 H5 I3C 1 c 110.5124; 10.558; 20.3568
90; 97.39; 90		2240.63Berger, G.; Robeyns, K.; Soubhye, J.; Wintjens, R.; Meyer, F.
Halogen bonding in a multi-connected 1,2,2-triiodo-alkene involving geminal and/or vicinal iodines: a crystallographic and DFT study
CrystEngComm, 2016, 18, 683
7223597 CIFC48 H58 Cu3 Mo8 N12 O50P -110.8729; 13.4826; 14.3867
87.715; 69.113; 72.445		1873.23Wang, Xiuli; Liu, Danna; Lin, Hongyan; Liu, Guocheng; Wang, Xiang; Le, Mao; Rong, Xing
pH, solvent and metal ion induced octamolybdate-based metal‒organic complexes decorated with a pyridyl-carboxylate ligand containing an amide group
CrystEngComm, 2016, 18, 888
7223598 CIFC12 H10 Cu Mo4 N3 O17P -19.9421; 10.2311; 11.0928
84.353; 89.574; 88.018		1122.19Wang, Xiuli; Liu, Danna; Lin, Hongyan; Liu, Guocheng; Wang, Xiang; Le, Mao; Rong, Xing
pH, solvent and metal ion induced octamolybdate-based metal‒organic complexes decorated with a pyridyl-carboxylate ligand containing an amide group
CrystEngComm, 2016, 18, 888
7223599 CIFC48 H50 Co3 Mo8 N12 O46P -112.1956; 12.8736; 14.2679
81.879; 71.871; 76.485		2064.2Wang, Xiuli; Liu, Danna; Lin, Hongyan; Liu, Guocheng; Wang, Xiang; Le, Mao; Rong, Xing
pH, solvent and metal ion induced octamolybdate-based metal‒organic complexes decorated with a pyridyl-carboxylate ligand containing an amide group
CrystEngComm, 2016, 18, 888
7223600 CIFC38 H48 Cl Cu N4 O S2P -111.443; 12.452; 15.01
71.585; 84.083; 68.386		1886.3Barman, Milan Kr.; Sinha, Ashish Kumar; Nembenna, Sharanappa
An efficient and recyclable thiourea-supported copper(i) chloride catalyst for azide‒alkyne cycloaddition reactions
Green Chem., 2016, 18, 2534
7223612 CIFC16 H15 Ag2 N3 O6P 61 2 216.5478; 16.5478; 12.4353
90; 90; 120		2949Zhang, Ting; Huang, Hua-Qi; Cheng, Xiao-Yue; Guo, Dong; Mei, Hong-Xin; Huang, Rong-Bin; Zheng, Lan-Sun
The synthesis and chiral crystal structures of two enantiomers of a Ag helical coordination polymer based on argentophilicity
CrystEngComm, 2016, 18, 670
7223613 CIFC16 H15 Ag2 N3 O6P 65 2 216.5272; 16.5272; 12.7024
90; 90; 120		3004.8Zhang, Ting; Huang, Hua-Qi; Cheng, Xiao-Yue; Guo, Dong; Mei, Hong-Xin; Huang, Rong-Bin; Zheng, Lan-Sun
The synthesis and chiral crystal structures of two enantiomers of a Ag helical coordination polymer based on argentophilicity
CrystEngComm, 2016, 18, 670
7223614 CIFC5 H4 I N OP 1 21/n 18.3971; 8.3248; 9.1806
90; 91.672; 90		641.49Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223615 CIFC45 H58 I N O12P -112.4821; 15.644; 23.8049
95.809; 99.751; 106.037		4348.9Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223616 CIFC52 H62 N2 O10P 1 21/n 112.559; 24.734; 14.682
90; 90.28; 90		4560.7Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223617 CIFC107 H135 N4 O23P -111.929; 12.698; 17.705
76.17; 75.84; 84.38		2522.8Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223618 CIFC48 H63 N O12P -19.136; 11.097; 22.784
92.12; 96.27; 103.65		2226.5Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223619 CIFC52 H78 N2 O14P 1 21/c 112.672; 24.549; 16.932
90; 103.57; 90		5120.2Puttreddy, Rakesh; Beyeh, Ngong Kodiah; Rissanen, Kari
Inclusion complexes of Cethyl-2-methylresorcinarene and pyridine N-oxides: breaking the C‒I⋯−O‒N+halogen bond by host‒guest complexation
CrystEngComm, 2016, 18, 793
7223621 CIFC46 H32 Co N4 O8P -19.706; 9.8389; 20.4971
91.899; 92.021; 109.147		1845.9Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223622 CIFC38 H32 Co2 N4 O9P -19.2805; 10.7128; 17.9162
103.41; 102.141; 94.265		1679.6Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223623 CIFC38 H32 Co N4 O12P -16.615; 10.2951; 14.1409
111.3; 92.619; 96.173		888.3Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223624 CIFC34 H30 N2 Ni O12P -19.3587; 9.74; 10.5441
68.781; 64.02; 88.873		794.29Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223625 CIFC19 H15 N2 Ni O4P -18.952; 10.1019; 10.887
90.87; 104.28; 111.042		884.61Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223626 CIFC34 H26 Cd N2 O10P -18.051; 10.0389; 18.4301
87.918; 79.934; 87.256		1464.4Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223627 CIFC30 H20 Cd2 N2 O10P 1 21/c 111.105; 19.2931; 15.0216
90; 125.643; 90		2615.5Mu, Bao; Huang, Ru-Dan
A series of coordination polymers with tuned terphenyl tetracarboxylates and bis-pyridyl ligands with different flexibilities manifesting fluorescence properties and photocatalytic activities
CrystEngComm, 2016, 18, 986
7223633 CIFC83 H75 Eu4 N O37P 42/n :221.2904; 21.2904; 19.3576
90; 90; 90		8774.4Zhao, Jie; Wang, Xin; Zhao, Jing; Luo, Rui; Shen, Xuan; Zhu, Dunru; Jing, Su
[Ln4@Ln4] matryoshka tetrahedron: a novel secondary building unit
CrystEngComm, 2016, 18, 863
7223634 CIFC83 H75 Gd4 N O37P 42/n :221.2232; 21.2232; 19.346
90; 90; 90		8713.9Zhao, Jie; Wang, Xin; Zhao, Jing; Luo, Rui; Shen, Xuan; Zhu, Dunru; Jing, Su
[Ln4@Ln4] matryoshka tetrahedron: a novel secondary building unit
CrystEngComm, 2016, 18, 863
7223635 CIFC83 H75 Dy4 N O37P 42/n :221.1619; 21.1619; 19.2599
90; 90; 90		8625.1Zhao, Jie; Wang, Xin; Zhao, Jing; Luo, Rui; Shen, Xuan; Zhu, Dunru; Jing, Su
[Ln4@Ln4] matryoshka tetrahedron: a novel secondary building unit
CrystEngComm, 2016, 18, 863
7223636 CIFC34 H26 Br Eu N4 O10P 1 21/c 18.8422; 20.71; 18.256
90; 111.944; 90		3100.9Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223637 CIFC34 H26 Br0.5 Cl0.5 Eu N4 O10P 1 21/c 18.8847; 20.515; 18.2437
90; 111.624; 90		3091.2Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223638 CIFC34 H26 Cl Eu N4 O10P 1 21/c 18.8828; 20.4075; 18.1897
90; 111.389; 90		3070.2Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223639 CIFC34 H26 Cl N4 O10 TbP 1 21/c 18.86; 20.463; 18.141
90; 111.41; 90		3062Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223640 CIFC34 H26 Br0.5 Cl0.5 N4 O10 TbP 1 21/c 18.844; 20.509; 18.1951
90; 111.645; 90		3067.5Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223641 CIFC34 H26 Br N4 O10 TbC 1 2/c 123.6157; 9.9206; 27.2126
90; 96.51; 90		6334.3Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223642 CIFC34 H26 Cl Gd N4 O10P 1 21/c 18.8072; 20.3895; 18.0976
90; 110.985; 90		3034.3Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223643 CIFC34 H26 Br0.5 Cl0.5 Gd N4 O10P 1 21/c 18.7794; 20.4692; 18.1663
90; 111.26; 90		3042.4Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223644 CIFC34 H26 Br Gd N4 O10P 1 21/c 18.865; 20.83; 18.31
90; 111.81; 90		3139Xu, Cong; Kirillov, Alexander M.; Shu, Yubo; Liu, Yan; Guo, Lirong; Yang, Lizi; Dou, Wei; Liu, Wei; Chen, Chunyang; Huang, Xin; Zhang, Jiayao; Liu, Weisheng
Photoluminescence enhancement induced by a halide anion encapsulation in a series of novel lanthanide(iii) coordination polymers
CrystEngComm, 2016, 18, 1190
7223645 CIFC28 H20 Cl4 N16 O Zn3P -19.8308; 12.7386; 14.0472
80.597; 84.851; 88.345		1728.32Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223646 CIFC20 H8 Cl3 N9 Zn2P b c m8.481; 17.5518; 18.3575
90; 90; 90		2732.64Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223647 CIFC42 H24 Cd6 Cl6 N24 O2R -321.4709; 21.4709; 11.969
90; 90; 120		4778.5Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223648 CIFC42 H24 Cd6 I6 N24 OR -322.0601; 22.0601; 11.9194
90; 90; 120		5023.4Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223649 CIFC14 H10 Br2 Cd2 N8 OP 1 21/c 113.269; 15.3212; 9.0739
90; 94.921; 90		1837.9Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223650 CIFC14 H10 Cd2 I4 N8P -17.5634; 10.2048; 14.7545
77.097; 84.449; 88.279		1104.79Yao, Peng-Fei; Liu, Han-Fu; Huang, Fu-Ping; Feng, Fang-lin; Qin, Xiao-Huan; Huang, Mei-Li; Yu, Qing; Bian, He-Dong
A family of Zn(ii)/Cd(ii) halide systems incorporating 5,5′-di(pyridin-2-yl)-3,3′-bi(1,2,4-triazole)
CrystEngComm, 2016, 18, 938
7223651 CIFC72 H104 O28 S8P 1 21/c 116.0033; 11.5923; 22.053
90; 94.549; 90		4078.3Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223652 CIFC84 H132 O30 S14P -113.312; 17.0039; 22.7649
105.34; 102.612; 106.369		4522.76Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223653 CIFC72 H92 O22 S6P -110.3128; 13.6528; 15.1819
113.311; 105.47; 95.699		1840.6Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223654 CIFC176 H272 O56 S24P -113.9805; 16.3367; 24.278
77.851; 73.707; 73.719		5056.3Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223655 CIFC92 H144 O28 S12P -113.5643; 14.1911; 15.9372
110.429; 109.634; 92.886		2658.4Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223656 CIFC95.8 H131.4 O26 S14P -112.9732; 14.665; 15.949
97.687; 112.271; 98.894		2712.1Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223657 CIFC86 H99.8 O23 S7P -112.3525; 13.8124; 15.0196
112.326; 112.595; 93.556		2122.7Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223658 CIFC152 H216 O44 S20P -110.6715; 16.8763; 24.6079
97.9; 102.264; 99.408		4203.7Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223659 CIFC72 H96 O20 S8P -112.5293; 13.2447; 13.6375
112.439; 109.559; 92.935		1929Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223660 CIFC80 H120 O24 S12P 1 21/n 113.6701; 16.5031; 21.1363
90; 99.896; 90		4697.38Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223661 CIFC156 H220 O42 S18P -113.887; 15.638; 23.205
99.446; 101.639; 114.753		4303.6Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223662 CIFC80 H112 O20 S8P -112.108; 13.5922; 26.446
88.602; 85.738; 83.463		4311.5Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223663 CIFC128 H108 N12 O8P -113.065; 14.1576; 15.2003
72.404; 76.963; 75.955		2564.45Pfeiffer, Constance R.; Feaster, Kyle A.; Dalgarno, Scott J.; Atwood, Jerry L.
Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes
CrystEngComm, 2016, 18, 222
7223717 CIFC12 H8 O3P 1 21/c 112.135; 3.979; 18.38
90; 91.4; 90		887.2Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223718 CIFC12 H7 Li O3P 1 21/c 114.953; 5.0185; 12.3691
90; 100.389; 90		913Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223719 CIFC12 H9 K O4P n a 217.3837; 30.138; 4.8965
90; 90; 90		1089.62Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223720 CIFC12 H9 Cs O4P n a 217.852; 29.89; 4.998
90; 90; 90		1173Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223721 CIFC31 H25 N3 O3P b c a20.9749; 19.1882; 13.2738
90; 90; 90		5342.3Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223722 CIFC17 H21 N3 O3P 1 21/n 19.0149; 9.7808; 18.7439
90; 102.981; 90		1610.47Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223723 CIFC31 H26 N2 O6P 1 21/n 115.3271; 8.3575; 20.696
90; 105.966; 90		2548.81Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223724 CIFC16 H15 N O3P -18.6; 8.6685; 9.647
101.959; 106.112; 105.087		636.12Saritemur, Gizem; Nomen Miralles, Laura; Husson, Deborah; Pitak, Mateusz B.; Coles, Simon J.; Wallis, John D.
Two modes of peri-interaction between an aldehyde group and a carboxylate anion in naphthalaldehydate salts
CrystEngComm, 2016, 18, 948
7223725 CIFC8 H14 Cl N5F d d 234.2012; 10.3247; 12.1234
90; 90; 90		4281Le, Thanh; Bhadbhade, Mohan; Gao, Jiabin; Hook, James M.; Marjo, Christopher E.
Persistence of a self-complementary N‒H⋯N tape motif in chloro-s-triazine crystals: crystal structures of simazine and atrazine herbicides and their polymorphic and inclusion behaviour
CrystEngComm, 2016, 18, 962
7223726 CIFC7 H12 Cl N5P 1 21/c 14.439; 11.98; 17.852
90; 94.04; 90		947Le, Thanh; Bhadbhade, Mohan; Gao, Jiabin; Hook, James M.; Marjo, Christopher E.
Persistence of a self-complementary N‒H⋯N tape motif in chloro-s-triazine crystals: crystal structures of simazine and atrazine herbicides and their polymorphic and inclusion behaviour
CrystEngComm, 2016, 18, 962
7223727 CIFC16 H28 Cl2 N10P b c a19.847; 9.616; 23.793
90; 90; 90		4540.9Le, Thanh; Bhadbhade, Mohan; Gao, Jiabin; Hook, James M.; Marjo, Christopher E.
Persistence of a self-complementary N‒H⋯N tape motif in chloro-s-triazine crystals: crystal structures of simazine and atrazine herbicides and their polymorphic and inclusion behaviour
CrystEngComm, 2016, 18, 962
7223728 CIFC20 H32 Cl10 N10P 1 21/c 111.908; 19.374; 15.441
90; 105.86; 90		3426.7Le, Thanh; Bhadbhade, Mohan; Gao, Jiabin; Hook, James M.; Marjo, Christopher E.
Persistence of a self-complementary N‒H⋯N tape motif in chloro-s-triazine crystals: crystal structures of simazine and atrazine herbicides and their polymorphic and inclusion behaviour
CrystEngComm, 2016, 18, 962
7223729 CIFC29 H33 Cl2 N3 O6P 1 21/c 114.8405; 10.2671; 20.6587
90; 110.219; 90		2953.8Nanubolu, Jagadeesh Babu; Ravikumar, Krishnan
Correlating the melting point alteration with the supramolecular structure in aripiprazole drug cocrystals
CrystEngComm, 2016, 18, 1024
7223730 CIFC29 H33 Cl2 N3 O4P 1 21/c 114.7282; 9.882; 20.8815
90; 111.174; 90		2834Nanubolu, Jagadeesh Babu; Ravikumar, Krishnan
Correlating the melting point alteration with the supramolecular structure in aripiprazole drug cocrystals
CrystEngComm, 2016, 18, 1024
7223731 CIFC29 H33 Cl2 N3 O4.29P 1 21/c 114.7513; 9.9206; 20.9131
90; 111.104; 90		2855.2Nanubolu, Jagadeesh Babu; Ravikumar, Krishnan
Correlating the melting point alteration with the supramolecular structure in aripiprazole drug cocrystals
CrystEngComm, 2016, 18, 1024
7223732 CIFC29 H33 Cl2 N3 O4P -16.9061; 9.4544; 22.484
96.056; 95.355; 100.696		1424.9Nanubolu, Jagadeesh Babu; Ravikumar, Krishnan
Correlating the melting point alteration with the supramolecular structure in aripiprazole drug cocrystals
CrystEngComm, 2016, 18, 1024
7223733 CIFC29 H33 Cl2 N3 O5.26P 1 21/c 114.7016; 9.9378; 20.9827
90; 111.121; 90		2859.7Nanubolu, Jagadeesh Babu; Ravikumar, Krishnan
Correlating the melting point alteration with the supramolecular structure in aripiprazole drug cocrystals
CrystEngComm, 2016, 18, 1024
7223734 CIFC26 H20 Cl8 Hg4 N6P -17.697; 15.919; 16.027
104.891; 101.344; 99.19		1814.35Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223735 CIFC26 H20 Br4 Hg2 N6P 1 21/c 18.7552; 14.1329; 23.646
90; 96.847; 90		2905Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223736 CIFC34 H25 Br2 Hg N5 OP 1 21/n 19.3733; 35.998; 9.8847
90; 104.978; 90		3222Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223737 CIFC26 H20 Hg I2 N6P -19.7571; 11.5338; 14.2949
68.98; 83.774; 68.968		1401.23Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223738 CIFC29 H28 Cl2 Hg N6 OP -18.764; 11.8787; 15.0315
73.615; 88.714; 88.11		1500.34Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223739 CIFC56 H48 Br8 Hg4 N12P -19.536; 10.9904; 15.8293
86.58; 73.062; 78.506		1555.19Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223740 CIFC26 H20 N6P 1 21/c 110.3079; 18.8288; 11.5821
90; 105.811; 90		2162.87Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223741 CIFC28 H24 N6P -19.6825; 11.376; 12.377
74.062; 76.504; 66.011		1186.1Mahmoudi, Ghodrat; Castiñeiras, Alfonso; Garczarek, Piotr; Bauzá, Antonio; Rheingold, Arnold L.; Kinzhybalo, Vasyl; Frontera, Antonio
Synthesis, X-ray characterization, DFT calculations and Hirshfeld surface analysis of thiosemicarbazone complexes of Mn+ions (n = 2, 3; M = Ni, Cd, Mn, Co and Cu)
CrystEngComm, 2016, 18, 1009
7223750 CIFC72.5 H54.5 Ca3.5 N2.5 O23C 1 2/c 128.281; 20.849; 30.699
90; 90.994; 90		18098Asha, K. S.; Makkitaya, Madhuri; Sirohi, Anshu; Yadav, Lalit; Sheet, Goutam; Mandal, Sukhendu
A series of s-block (Ca, Sr and Ba) metal‒organic frameworks: synthesis and structure‒property correlation
CrystEngComm, 2016, 18, 1046
7223751 CIFC56 H43 N O14.5 Sr2.5C 1 2/c 118.2197; 31.5978; 29.862
90; 101.311; 90		16857.7Asha, K. S.; Makkitaya, Madhuri; Sirohi, Anshu; Yadav, Lalit; Sheet, Goutam; Mandal, Sukhendu
A series of s-block (Ca, Sr and Ba) metal‒organic frameworks: synthesis and structure‒property correlation
CrystEngComm, 2016, 18, 1046
7223752 CIFC29 H17 Ba N O7P n a 217.2993; 19.3615; 26.0984
90; 90; 90		3688.4Asha, K. S.; Makkitaya, Madhuri; Sirohi, Anshu; Yadav, Lalit; Sheet, Goutam; Mandal, Sukhendu
A series of s-block (Ca, Sr and Ba) metal‒organic frameworks: synthesis and structure‒property correlation
CrystEngComm, 2016, 18, 1046
7223753 CIFC16 H8 Li2 O7P 1 21/c 118.9997; 9.4546; 7.4275
90; 95.743; 90		1327.54Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223754 CIFC16 H8 Li2 O7P 1 21/c 119.0868; 9.4849; 7.4588
90; 94.757; 90		1345.66Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223755 CIFC16 H7 Li O6P 1 21/c 18.0799; 10.6463; 14.6639
90; 102.507; 90		1231.47Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223756 CIFC16 H7 Li O6P 1 21/c 18.1681; 10.6558; 14.7002
90; 101.68; 90		1252.98Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223757 CIFC14 H10 Li2 O6P 1 21/c 18.0703; 5.1497; 14.7759
90; 95.073; 90		611.68Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223758 CIFC7 H5 Li O3P 1 21/c 18.0719; 5.1821; 14.8188
90; 94.926; 90		617.57Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223759 CIFC14 H10 Li2 O6P n m a7.1641; 16.1044; 10.7351
90; 90; 90		1238.55Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223760 CIFC7 H5 Li O3P n m a7.1681; 16.0902; 10.7456
90; 90; 90		1239.36Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223761 CIFC14 H9 Li O5P 21 21 213.8011; 15.9753; 18.0272
90; 90; 90		1094.68Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223762 CIFC14 H7.5 Li O4.25P 21 21 213.6746; 16.1112; 18.1111
90; 90; 90		1072.22Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223763 CIFC14 H8 Li N O6P 21 21 214.8535; 13.0952; 18.9644
90; 90; 90		1205.33Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223764 CIFC14 H8 Li N O6P 21 21 214.8953; 13.2668; 19.1081
90; 90; 90		1240.97Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223765 CIFC14 H16 Li2 O9P -15.0112; 7.5031; 21.0358
97.619; 91.892; 108.338		741.79Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223766 CIFC14 H7 N O5P 1 21/n 17.3423; 10.0879; 14.4961
90; 89.137; 90		1073.58Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223767 CIFC14 H7 N O5P 1 21/n 17.4696; 10.1464; 14.5732
90; 90.118; 90		1104.49Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223768 CIFC H Li O2C 1 2/c 112.0297; 12.0413; 13.5174
90; 100.597; 90		1924.64Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223769 CIFC H Li O2C 1 2/c 112.0519; 12.0497; 13.5108
90; 101.003; 90		1925.99Tominaka, Satoshi; Yeung, Hamish H.-M.; Henke, Sebastian; Cheetham, Anthony K.
Coordination environments and π-conjugation in dense lithium coordination polymers
CrystEngComm, 2016, 18, 398
7223770 CIFC75 H47 N5 O9 Zn2C 1 2/c 128.525; 29.966; 14.784
90; 109.02; 90		11947.1Liu, Yue; Chen, Dashu; Li, Xingyu; Yu, Ziyang; Xia, Qiansu; Liang, Desheng; Xing, Hongzhu
Visible-light-induced controlled radical polymerization of methacrylates mediated by a pillared-layer metal‒organic framework
Green Chem., 2016, 18, 1475
7223799 CIFC23 H26 O6 SP 21 21 215.8253; 8.3302; 42.609
90; 90; 90		2067.6Pal, Kumar Bhaskar; Sarkar, Vikramjit; Mukhopadhyay, Balaram
Hydrogen bonding-induced conformational change in a crystalline sugar derivative
CrystEngComm, 2016, 18, 1156
7223800 CIFC13 H18 O5 SP 1 21 15.1361; 8.6117; 15.789
90; 96.403; 90		694Pal, Kumar Bhaskar; Sarkar, Vikramjit; Mukhopadhyay, Balaram
Hydrogen bonding-induced conformational change in a crystalline sugar derivative
CrystEngComm, 2016, 18, 1156
7223801 CIFC16 H23 O5.5 SP 1 21 111.1679; 7.7832; 19.3582
90; 100.192; 90		1656.1Pal, Kumar Bhaskar; Sarkar, Vikramjit; Mukhopadhyay, Balaram
Hydrogen bonding-induced conformational change in a crystalline sugar derivative
CrystEngComm, 2016, 18, 1156
7223834 CIFC26 H38 N4 O6P 1 21 110.5276; 11.0184; 12.8075
90; 100.792; 90		1459.36Podder, Debasish; Sasmal, Supriya; Maji, Krishnendu; Haldar, Debasish
Supramolecular tryptophan-zipper forms a tripeptide as a regular proton transporter
CrystEngComm, 2016, 18, 4109
7223835 CIFC27 H42 N4 O7P 21 21 218.9295; 15.865; 21.5604
90; 90; 90		3054.39Podder, Debasish; Sasmal, Supriya; Maji, Krishnendu; Haldar, Debasish
Supramolecular tryptophan-zipper forms a tripeptide as a regular proton transporter
CrystEngComm, 2016, 18, 4109
7223836 CIFC27 H44 OP 6528.2798; 28.2798; 5.9321
90; 90; 120		4108.6Wang, Jian-Rong; Zhu, Bingqing; Yu, Qihui; Mei, Xuefeng
Selective crystallization of vitamin D3for the preparation of novel conformational polymorphs with distinctive chemical stability
CrystEngComm, 2016, 18, 1101
7223837 CIFC4 H6 O2 Pd S4P 1 21/c 16.2713; 13.5593; 10.7931
90; 97.635; 90		909.65Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223838 CIFC6 H10 O2 Pd S4P b c a7.5034; 7.2125; 20.7854
90; 90; 90		1124.87Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223839 CIFC8 H14 O2 Pd S4P -17.4778; 9.5272; 9.8084
74.832; 86.458; 76.292		655.22Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223840 CIFC8 H14 O2 Pd S4P 1 21/n 19.9077; 5.872; 11.9621
90; 102.752; 90		678.77Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223841 CIFC10 H18 O2 Pd S4P -15.7038; 6.7822; 10.5967
72.42; 78.467; 79.852		379.94Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223842 CIFC10 H18 O2 Pd S4P -16.0243; 8.0461; 8.9366
111.05; 99.851; 103.836		376.42Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223843 CIFC14 H26 O2 Pd S4P -17.0663; 8.4457; 9.2536
63.74; 73.752; 83.782		475.4Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223844 CIFC14 H26 O2 Pd S4P -16.1398; 6.7176; 11.9393
90.02; 99.397; 95.377		483.63Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223845 CIFC12 H22 O2 Pd S4P -16.882; 7.3531; 10.0455
70.305; 70.788; 67.164		429.42Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223846 CIFC12 H22 O2 Pd S4P -16.5622; 6.8643; 9.8385
84.811; 76.424; 83.388		427Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223847 CIFC12 H22 O2 Pd S4P -16.2746; 6.3302; 11.4138
79.69; 88.152; 86.065		444.89Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223848 CIFC14 H26 O2 Pd S4P -16.8083; 7.5446; 10.4837
101.008; 98.983; 112.048		474.33Tan, Yee Seng; Halim, Siti Nadiah Abdul; Molloy, Kieran C.; Sudlow, Anna L.; Otero-de-la-Roza, A.; Tiekink, Edward R. T.
Persistence of C‒H⋯π(chelate ring) interactions in the crystal structures of Pd(S2COR)2. The utility of Pd(S2COR)2as precursors for palladium sulphide materials
CrystEngComm, 2016, 18, 1105
7223851 CIFC30 H21 F6 Mn O6R -3 :H18.583; 18.583; 14.503
90; 90; 120		4337.3Carli, Stefano; Benazzi, Elisabetta; Casarin, Laura; Bernardi, Tatiana; Bertolasi, Valerio; Argazzi, Roberto; Caramori, Stefano; Bignozzi, Carlo Alberto
On the stability of manganese tris(β-diketonate) complexes as redox mediators in DSSCs.
Physical chemistry chemical physics : PCCP, 2016, 18, 5949-5956
7223852 CIFC28 H40 Cl Mn N2 O8C 1 2/c 116.325; 17.663; 12.491
90; 115.434; 90		3252.7Carli, Stefano; Benazzi, Elisabetta; Casarin, Laura; Bernardi, Tatiana; Bertolasi, Valerio; Argazzi, Roberto; Caramori, Stefano; Bignozzi, Carlo Alberto
On the stability of manganese tris(β-diketonate) complexes as redox mediators in DSSCs.
Physical chemistry chemical physics : PCCP, 2016, 18, 5949-5956
7223853 CIFC38 H40 F4 Mn N2 O4C 1 2/c 118.2229; 19.0407; 11.7031
90; 115.785; 90		3656.4Carli, Stefano; Benazzi, Elisabetta; Casarin, Laura; Bernardi, Tatiana; Bertolasi, Valerio; Argazzi, Roberto; Caramori, Stefano; Bignozzi, Carlo Alberto
On the stability of manganese tris(β-diketonate) complexes as redox mediators in DSSCs.
Physical chemistry chemical physics : PCCP, 2016, 18, 5949-5956
7223863 CIFC45 H35 Cd3 N O15R -3 :H14.07; 14.07; 19.864
90; 90; 120		3406Fernández, Belén; Beobide, Garikoitz; Sánchez, Ignacio; Carrasco-Marín, Francisco; Seco, José M.; Calahorro, Antonio J.; Cepeda, Javier; Rodríguez-Diéguez, Antonio
Controlling interpenetration for tuning porosity and luminescence properties of flexible MOFs based on biphenyl-4,4′-dicarboxylic acid
CrystEngComm, 2016, 18, 1282
7223864 CIFC69 H69 N9 O17 Zn3C 1 2/c 147.928; 13.828; 26.187
90; 114.491; 90		15794Fernández, Belén; Beobide, Garikoitz; Sánchez, Ignacio; Carrasco-Marín, Francisco; Seco, José M.; Calahorro, Antonio J.; Cepeda, Javier; Rodríguez-Diéguez, Antonio
Controlling interpenetration for tuning porosity and luminescence properties of flexible MOFs based on biphenyl-4,4′-dicarboxylic acid
CrystEngComm, 2016, 18, 1282
7223865 CIFC61 H75 N11 O15 Zn2P -115.174; 15.185; 18.174
81.094; 84.734; 78.952		4052.1Fernández, Belén; Beobide, Garikoitz; Sánchez, Ignacio; Carrasco-Marín, Francisco; Seco, José M.; Calahorro, Antonio J.; Cepeda, Javier; Rodríguez-Diéguez, Antonio
Controlling interpenetration for tuning porosity and luminescence properties of flexible MOFs based on biphenyl-4,4′-dicarboxylic acid
CrystEngComm, 2016, 18, 1282
7223866 CIFC66 H88 N8 O25 Zn4P n n m17.256; 23.227; 25.426
90; 90; 90		10191Fernández, Belén; Beobide, Garikoitz; Sánchez, Ignacio; Carrasco-Marín, Francisco; Seco, José M.; Calahorro, Antonio J.; Cepeda, Javier; Rodríguez-Diéguez, Antonio
Controlling interpenetration for tuning porosity and luminescence properties of flexible MOFs based on biphenyl-4,4′-dicarboxylic acid
CrystEngComm, 2016, 18, 1282
7223867 CIFC24 H54 Co6 F12 N8 O43I 41/a m d17.726; 17.726; 38.491
90; 90; 90		12094Cai, Song-Liang; Zheng, Sheng-Run; Fan, Jun; Zeng, Rong-Hua; Zhang, Wei-Guang
Two new three-dimensional metal‒organic frameworks with 4-connected diamondoid and unusual (6,16)-connected net topologies based on planar tetranuclear squares as secondary building units
CrystEngComm, 2016, 18, 1174
7223868 CIFC42 H24 F18 Mn7 N15 O24I -4 3 d32.9672; 32.9672; 32.9672
90; 90; 90		35829.9Cai, Song-Liang; Zheng, Sheng-Run; Fan, Jun; Zeng, Rong-Hua; Zhang, Wei-Guang
Two new three-dimensional metal‒organic frameworks with 4-connected diamondoid and unusual (6,16)-connected net topologies based on planar tetranuclear squares as secondary building units
CrystEngComm, 2016, 18, 1174
7223869 CIFC72 H62 Co4.5 N34 O12 W3P 1 21/c 120.2531; 19.4998; 29.3833
90; 122.99; 90		9733.4Chorazy, Szymon; Hoczek, Anna; Kubicki, Maciej; Tokoro, Hiroko; Ohkoshi, Shin-ichi; Sieklucka, Barbara; Podgajny, Robert
The solvent effect on the structural and magnetic features of bidentate ligand-capped {CoII9[WV(CN)8]6} single-molecule magnets
CrystEngComm, 2016, 18, 1495
7223870 CIFC164.5 H169.5 Co9 N72.5 O28.5 W6P -119.0923; 20.3195; 31.5482
72.427; 77.063; 68.621		10775.3Chorazy, Szymon; Hoczek, Anna; Kubicki, Maciej; Tokoro, Hiroko; Ohkoshi, Shin-ichi; Sieklucka, Barbara; Podgajny, Robert
The solvent effect on the structural and magnetic features of bidentate ligand-capped {CoII9[WV(CN)8]6} single-molecule magnets
CrystEngComm, 2016, 18, 1495
7223871 CIFC165 H164.5 Co9 N69.5 O24 W6C 1 c 119.4379; 35.2593; 30.9195
90; 91.67; 90		21182.2Chorazy, Szymon; Hoczek, Anna; Kubicki, Maciej; Tokoro, Hiroko; Ohkoshi, Shin-ichi; Sieklucka, Barbara; Podgajny, Robert
The solvent effect on the structural and magnetic features of bidentate ligand-capped {CoII9[WV(CN)8]6} single-molecule magnets
CrystEngComm, 2016, 18, 1495
7223872 CIFC26 H34 O3 SP 21 21 29.7748; 36.406; 6.5704
90; 90; 90		2338.2Huang, Mingming; Hu, Liangzhen; Shen, Hang; Liu, Qing; Hussain, Muhammad Ijaz; Pan, Jing; Xiong, Yan
Sulfination of alcohols with sodium sulfinates promoted by BF3·OEt2: an unexpected access
Green Chem., 2016, 18, 1874
7223876 CIFC23 H27 Cl2 N3 O2P 1 21/n 116.6133; 6.9533; 19.4632
90; 106.99; 90		2150.2Zeidan, T. A.; Trotta, J. T.; Tilak, P. A.; Oliveira, M. A.; Chiarella, R. A.; Foxman, B. M.; Almarsson, Ö.; Hickey, M. B.
An unprecedented case of dodecamorphism: the twelfth polymorph of aripiprazole formed by seeding with its active metabolite
CrystEngComm, 2016, 18, 1486
7223877 CIFC24.5 H30.5 Cl2 N3 O2.5P -17.7282; 10.7005; 15.4954
83.863; 78.191; 73.576		1201.46Zeidan, T. A.; Trotta, J. T.; Tilak, P. A.; Oliveira, M. A.; Chiarella, R. A.; Foxman, B. M.; Almarsson, Ö.; Hickey, M. B.
An unprecedented case of dodecamorphism: the twelfth polymorph of aripiprazole formed by seeding with its active metabolite
CrystEngComm, 2016, 18, 1486
7223878 CIFC30 H12 N6 O3C 1 2/c 114.4563; 24.746; 14.626
90; 112.294; 90		4841.1Köç, Muzaffer; Zorlu, Yunus; İşci, Ümit; Berber, Savaş; Ahsen, Vefa; Dumoulin, Fabienne
A library of dimeric and trimeric phthalonitriles linked by a single aromatic ring: comparative structural and DFT investigations
CrystEngComm, 2016, 18, 1416
7223879 CIFC22 H10 N4 O2P -18.0768; 8.5809; 13.4764
74.672; 88.214; 77.262		878.24Köç, Muzaffer; Zorlu, Yunus; İşci, Ümit; Berber, Savaş; Ahsen, Vefa; Dumoulin, Fabienne
A library of dimeric and trimeric phthalonitriles linked by a single aromatic ring: comparative structural and DFT investigations
CrystEngComm, 2016, 18, 1416
7223880 CIFC30 H26 N4 O2P 1 21/n 110.2611; 13.4117; 18.9648
90; 101.601; 90		2556.6Köç, Muzaffer; Zorlu, Yunus; İşci, Ümit; Berber, Savaş; Ahsen, Vefa; Dumoulin, Fabienne
A library of dimeric and trimeric phthalonitriles linked by a single aromatic ring: comparative structural and DFT investigations
CrystEngComm, 2016, 18, 1416
7223881 CIFC22 H10 N4 O2P n a 2120.9421; 5.0644; 32.897
90; 90; 90		3489Köç, Muzaffer; Zorlu, Yunus; İşci, Ümit; Berber, Savaş; Ahsen, Vefa; Dumoulin, Fabienne
A library of dimeric and trimeric phthalonitriles linked by a single aromatic ring: comparative structural and DFT investigations
CrystEngComm, 2016, 18, 1416
7223882 CIFC22 H10 N4 O2C 1 2/c 113.7511; 7.3953; 17.5013
90; 91.983; 90		1778.7Köç, Muzaffer; Zorlu, Yunus; İşci, Ümit; Berber, Savaş; Ahsen, Vefa; Dumoulin, Fabienne
A library of dimeric and trimeric phthalonitriles linked by a single aromatic ring: comparative structural and DFT investigations
CrystEngComm, 2016, 18, 1416
7223893 CIFC36 H35 La N4 O13P -19.8229; 11.4914; 16.3886
94.801; 103.133; 97.661		1772.97Karmakar, Anirban; Hazra, Susanta; Guedes da Silva, M. Fátima C.; Paul, Anup; Pombeiro, Armando J. L.
Nanoporous lanthanide metal‒organic frameworks as efficient heterogeneous catalysts for the Henry reaction
CrystEngComm, 2016, 18, 1337
7223894 CIFC36 H35 Ce N4 O13P -19.8826; 11.5594; 16.3655
94.257; 103.951; 97.86		1786.14Karmakar, Anirban; Hazra, Susanta; Guedes da Silva, M. Fátima C.; Paul, Anup; Pombeiro, Armando J. L.
Nanoporous lanthanide metal‒organic frameworks as efficient heterogeneous catalysts for the Henry reaction
CrystEngComm, 2016, 18, 1337
7223895 CIFC31 H43 La N6 O14I a -327.0059; 27.0059; 27.0059
90; 90; 90		19695.9Karmakar, Anirban; Hazra, Susanta; Guedes da Silva, M. Fátima C.; Paul, Anup; Pombeiro, Armando J. L.
Nanoporous lanthanide metal‒organic frameworks as efficient heterogeneous catalysts for the Henry reaction
CrystEngComm, 2016, 18, 1337
7223896 CIFC29 H36 Ce N5 O13I a -326.921; 26.921; 26.921
90; 90; 90		19511Karmakar, Anirban; Hazra, Susanta; Guedes da Silva, M. Fátima C.; Paul, Anup; Pombeiro, Armando J. L.
Nanoporous lanthanide metal‒organic frameworks as efficient heterogeneous catalysts for the Henry reaction
CrystEngComm, 2016, 18, 1337
7223897 CIFC23 H24 N5 O13 SmI a -326.681; 26.681; 26.681
90; 90; 90		18994Karmakar, Anirban; Hazra, Susanta; Guedes da Silva, M. Fátima C.; Paul, Anup; Pombeiro, Armando J. L.
Nanoporous lanthanide metal‒organic frameworks as efficient heterogeneous catalysts for the Henry reaction
CrystEngComm, 2016, 18, 1337
7223898 CIFC33 H43 N8 O13.17 SmR -3 :H25.917; 25.917; 30.915
90; 90; 120		17983Masuya-Suzuki, Atsuko; Matsubara, Nozomi; Karashimada, Ryunosuke; Hoshino, Hitoshi; Iki, Nobuhiko
Topological modulation of the porous structure of a coordination polymer constructed from a flexible building block via framework‒guest interaction during self-assembly
CrystEngComm, 2016, 18, 872
7223899 CIFC30.33 H36.53 N7 O12.5 SmR -3 :H25.758; 25.758; 30.055
90; 90; 120		17269Masuya-Suzuki, Atsuko; Matsubara, Nozomi; Karashimada, Ryunosuke; Hoshino, Hitoshi; Iki, Nobuhiko
Topological modulation of the porous structure of a coordination polymer constructed from a flexible building block via framework‒guest interaction during self-assembly
CrystEngComm, 2016, 18, 872
7223915 CIFC32 H42 Cu2 N20 O13I 1 2/a 18.2134; 16.974; 19.396
90; 101.13; 90		2653.2Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223916 CIFC16 H16 Co N10 O4P 1 21/c 14.8427; 9.4938; 20.097
90; 92.37; 90		923.2Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223917 CIFC16 H16 Mn N10 O4P 1 21/c 14.914; 9.3923; 20.417
90; 92.66; 90		941.3Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223918 CIFC16 H16 Cd N10 O4P 1 21/c 14.9534; 9.1796; 20.865
90; 93.9; 90		946.5Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223919 CIFC16 H16 N10 O4 PbP c c n10.487; 23.35; 8.3772
90; 90; 90		2051.3Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223920 CIFC16 H28 Co N10 O10P -17.7702; 9.0412; 9.2461
94.47; 107.46; 95.08		613.5Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223921 CIFC16 H28 Mn N10 O10P -17.8231; 9.0961; 9.2962
94.66; 107.53; 95.54		623.6Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223922 CIFC16 H28 N10 Ni O10P -17.7318; 8.9961; 9.1815
94.4; 107.22; 95.01		604.1Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223923 CIFC16 H28 N10 O10 ZnP -17.7881; 9.038; 9.1899
94.47; 107.49; 95.27		610.5Yu, Tiantian; Wang, Shimin; Li, Xuemin; Gao, Xiaoli; Zhou, Chunlin; Cheng, Jiajia; Li, Baojun; Li, Jinpeng; Chang, Junbiao; Hou, Hongwei; Liu, Zhongyi
Roles of temperature, solvent, M/L ratios and anion in preparing complexes containing a Himta ligand
CrystEngComm, 2016, 18, 1350
7223924 CIFC62 H46 N14 O14 Zn2C 1 2/c 130.8851; 17.4665; 20.3272
90; 127.705; 90		8675.7Zhang, Le; Feng, Xue Feng; Meng, Pan Pan; Gong, Le Le; Luo, Feng
Thermodynamically stable MOF showing a highly rare four-connectedhxg-d-4-Cccmnet with self-penetration, polyrotaxane, and polycatenane multi-features
CrystEngComm, 2016, 18, 1693
7223925 CIFC31 H21 N7 O6 ZnP -110.882; 11.386; 20.627
100.75; 103.307; 103.024		2345.3Zhang, Le; Feng, Xue Feng; Meng, Pan Pan; Gong, Le Le; Luo, Feng
Thermodynamically stable MOF showing a highly rare four-connectedhxg-d-4-Cccmnet with self-penetration, polyrotaxane, and polycatenane multi-features
CrystEngComm, 2016, 18, 1693
7223926 CIFC28 H28 Cu2 Dy N5 O20P -19.672; 13.729; 13.997
94.881; 102.916; 101.498		1758.8Gawai, U. P.; Khawal, H. A.; Shripathi, T.; Dole, B. N.
A study on the synthesis, pair distribution function and diverse properties of cobalt doped ZnS nanowires
CrystEngComm, 2016, 18, 1439
7223939 CIFC3 H7 N O2P 21 21 215.779; 6.031; 12.318
90; 90; 90		429.3Tsuboi, Chiaki; Aburaya, Kazuaki; Kimura, Fumiko; Maeyama, Masataka; Kimura, Tsunehisa
Single-crystal structure determination from microcrystalline powders (σim 5 μm) by an orientation attachment mountable on an in-house X-ray diffractometer
CrystEngComm, 2016, 18, 2404
7223940 CIFC3 H7 N O2P 21 21 215.7772; 6.035; 12.316
90; 90; 90		429.4Tsuboi, Chiaki; Aburaya, Kazuaki; Kimura, Fumiko; Maeyama, Masataka; Kimura, Tsunehisa
Single-crystal structure determination from microcrystalline powders (σim 5 μm) by an orientation attachment mountable on an in-house X-ray diffractometer
CrystEngComm, 2016, 18, 2404
7223958 CIFC11 H5 F5 I NP 1 21/c 111.9726; 9.2769; 11.5812
90; 112.372; 90		1189.49Vasylyeva, Vera; Catalano, Luca; Nervi, Carlo; Gobetto, Roberto; Metrangolo, Pierangelo; Resnati, Giuseppe
Characteristic redshift and intensity enhancement as far-IR fingerprints of the halogen bond involving aromatic donors
CrystEngComm, 2016, 18, 2247
7223959 CIFC12 H7 F5 I NP 1 21/n 18.0031; 12.031; 13.4501
90; 100.731; 90		1272.4Vasylyeva, Vera; Catalano, Luca; Nervi, Carlo; Gobetto, Roberto; Metrangolo, Pierangelo; Resnati, Giuseppe
Characteristic redshift and intensity enhancement as far-IR fingerprints of the halogen bond involving aromatic donors
CrystEngComm, 2016, 18, 2247
7223960 CIFC11 H5 Br F5 NP 1 21/c 18.8544; 9.3356; 14.0154
90; 101.478; 90		1135.36Vasylyeva, Vera; Catalano, Luca; Nervi, Carlo; Gobetto, Roberto; Metrangolo, Pierangelo; Resnati, Giuseppe
Characteristic redshift and intensity enhancement as far-IR fingerprints of the halogen bond involving aromatic donors
CrystEngComm, 2016, 18, 2247
7223961 CIFC9 H8 F5 I NP 1 21/n 111.7434; 5.8599; 16.7329
90; 99.173; 90		1136.75Vasylyeva, Vera; Catalano, Luca; Nervi, Carlo; Gobetto, Roberto; Metrangolo, Pierangelo; Resnati, Giuseppe
Characteristic redshift and intensity enhancement as far-IR fingerprints of the halogen bond involving aromatic donors
CrystEngComm, 2016, 18, 2247
7223962 CIFC10 H21 N5 Na O11 PP 21 21 216.5585; 7.047; 38.869
90; 90; 90		1796.4Yang, Pengpeng; Lin, Chenguang; Zhuang, Wei; Wen, Qingshi; Zou, Fengxia; Zhou, Jingwei; Wu, Jinglan; Ying, Hanjie
Insight into a direct solid‒solid transformation: a potential approach for the removal of residual solvents
CrystEngComm, 2016, 18, 1699
7223963 CIFC11 H21 N5 Na O10 PP 21 21 216.5021; 7.0943; 39.198
90; 90; 90		1808.1Yang, Pengpeng; Lin, Chenguang; Zhuang, Wei; Wen, Qingshi; Zou, Fengxia; Zhou, Jingwei; Wu, Jinglan; Ying, Hanjie
Insight into a direct solid‒solid transformation: a potential approach for the removal of residual solvents
CrystEngComm, 2016, 18, 1699
7223964 CIFC6 H6 O6 UP n n m13.314; 9.7055; 7.0691
90; 90; 90		913.46Klepov, Vladislav V.; Vologzhanina, Anna V.; Alekseev, Evgeny V.; Pushkin, Denis V.; Serezhkina, Larisa B.; Sergeeva, Olga A.; Knyazev, Aleksandr V.; Serezhkin, Viktor N.
Structural diversity of uranyl acrylates
CrystEngComm, 2016, 18, 1723
7223965 CIFC6 H10.44 O8.22 UR -3 :H19.5621; 19.5621; 8.7321
90; 90; 120		2893.9Klepov, Vladislav V.; Vologzhanina, Anna V.; Alekseev, Evgeny V.; Pushkin, Denis V.; Serezhkina, Larisa B.; Sergeeva, Olga A.; Knyazev, Aleksandr V.; Serezhkin, Viktor N.
Structural diversity of uranyl acrylates
CrystEngComm, 2016, 18, 1723
7223966 CIFC6 H12 O9 UP 1 21/c 111.6745; 12.4709; 16.003
90; 148.27; 90		1225.3Klepov, Vladislav V.; Vologzhanina, Anna V.; Alekseev, Evgeny V.; Pushkin, Denis V.; Serezhkina, Larisa B.; Sergeeva, Olga A.; Knyazev, Aleksandr V.; Serezhkin, Viktor N.
Structural diversity of uranyl acrylates
CrystEngComm, 2016, 18, 1723
7223967 CIFC6 H10 O8 UP 1 21/n 110.7059; 7.7322; 13.5945
90; 107.093; 90		1075.65Klepov, Vladislav V.; Vologzhanina, Anna V.; Alekseev, Evgeny V.; Pushkin, Denis V.; Serezhkina, Larisa B.; Sergeeva, Olga A.; Knyazev, Aleksandr V.; Serezhkin, Viktor N.
Structural diversity of uranyl acrylates
CrystEngComm, 2016, 18, 1723
7223968 CIFC6 H10 O8 UC 1 2/m 110.724; 7.721; 6.897
90; 107.246; 90		545.4Klepov, Vladislav V.; Vologzhanina, Anna V.; Alekseev, Evgeny V.; Pushkin, Denis V.; Serezhkina, Larisa B.; Sergeeva, Olga A.; Knyazev, Aleksandr V.; Serezhkin, Viktor N.
Structural diversity of uranyl acrylates
CrystEngComm, 2016, 18, 1723
7223969 CIFC11 H13 N5 O5 ZnP 1 21/c 110.097; 12.8101; 10.9229
90; 102.581; 90		1378.9Gao, Wei; Li, Peng; Liu, Feng; Zhang, Xiu-Mei; Liu, Jie-Ping
Four metal‒organic frameworks based on the 5-(1H-tetrazol-5-yl)isophthalic acid ligand: luminescence and magnetic properties
CrystEngComm, 2016, 18, 1523
7223970 CIFC12 H16 Cd2 N5 O8.5P 1 21/m 110.4622; 7.187; 13.4544
90; 112.694; 90		933.34Gao, Wei; Li, Peng; Liu, Feng; Zhang, Xiu-Mei; Liu, Jie-Ping
Four metal‒organic frameworks based on the 5-(1H-tetrazol-5-yl)isophthalic acid ligand: luminescence and magnetic properties
CrystEngComm, 2016, 18, 1523
7223971 CIFC9 H7 Mn N4 Na O6C 1 2/c 119.571; 11.0278; 13.2983
90; 124.084; 90		2377.1Gao, Wei; Li, Peng; Liu, Feng; Zhang, Xiu-Mei; Liu, Jie-Ping
Four metal‒organic frameworks based on the 5-(1H-tetrazol-5-yl)isophthalic acid ligand: luminescence and magnetic properties
CrystEngComm, 2016, 18, 1523
7223972 CIFC18 H38 Mn3 N8 O24P -17.3088; 10.1375; 12.0815
78.884; 77.512; 78.615		846.18Gao, Wei; Li, Peng; Liu, Feng; Zhang, Xiu-Mei; Liu, Jie-Ping
Four metal‒organic frameworks based on the 5-(1H-tetrazol-5-yl)isophthalic acid ligand: luminescence and magnetic properties
CrystEngComm, 2016, 18, 1523
7223973 CIFC28 H39 N6 O11.5 SP b c a24.029; 10.9805; 24.3497
90; 90; 90		6424.7Abraham, Anuji; Apperley, David C.; Byard, Stephen J.; Ilott, Andrew J.; Robbins, Andrew J.; Zorin, Vadim; Harris, Robin K.; Hodgkinson, Paul
Characterising the role of water in sildenafil citrate by NMR crystallography
CrystEngComm, 2016, 18, 1054
7223974 CIFC22 H26 N2 O4 SP 21 21 219.3387; 13.9027; 16.555
90; 90; 90		2149.39Stepanovs, D.; Jure, M.; Gosteva, M.; Popelis, J.; Kiselovs, G.; Mishnev, A.
Crystal structures and physicochemical properties of diltiazem base and its acetylsalicylate, nicotinate andl-malate salts
CrystEngComm, 2016, 18, 1235
7223975 CIFC31 H36 N2 O9 SP 21 21 219.9411; 10.7606; 28.5926
90; 90; 90		3058.61Stepanovs, D.; Jure, M.; Gosteva, M.; Popelis, J.; Kiselovs, G.; Mishnev, A.
Crystal structures and physicochemical properties of diltiazem base and its acetylsalicylate, nicotinate andl-malate salts
CrystEngComm, 2016, 18, 1235
7223976 CIFC28 H31 N3 O6 SP 1 21 18.7897; 6.1726; 25.1531
90; 91.5255; 90		1364.21Stepanovs, D.; Jure, M.; Gosteva, M.; Popelis, J.; Kiselovs, G.; Mishnev, A.
Crystal structures and physicochemical properties of diltiazem base and its acetylsalicylate, nicotinate andl-malate salts
CrystEngComm, 2016, 18, 1235
7223977 CIFC26 H32 N2 O9 SP 21 21 215.8962; 9.032; 50.5074
90; 90; 90		2689.75Stepanovs, D.; Jure, M.; Gosteva, M.; Popelis, J.; Kiselovs, G.; Mishnev, A.
Crystal structures and physicochemical properties of diltiazem base and its acetylsalicylate, nicotinate andl-malate salts
CrystEngComm, 2016, 18, 1235
7223978 CIFC63.4 H52.8 N4 O2 SnR -3 :H36.4984; 36.4984; 10.5148
90; 90; 120		12130.5Wang, S.; Knowles, G. P.; Chaffee, A. L.; Langford, S. J.
Selective CO2uptake and vapor adsorption study within Sn(iv) porphyrin crystals
CrystEngComm, 2016, 18, 1515
7223979 CIFC60 H44 Br2 N4 O2 SnR -3 :H36.626; 36.626; 10.4295
90; 90; 120		12116.4Wang, S.; Knowles, G. P.; Chaffee, A. L.; Langford, S. J.
Selective CO2uptake and vapor adsorption study within Sn(iv) porphyrin crystals
CrystEngComm, 2016, 18, 1515
7223980 CIFC60 H44 N6 O6 SnR -3 :H37.09; 37.09; 10.1013
90; 90; 120		12034.3Wang, S.; Knowles, G. P.; Chaffee, A. L.; Langford, S. J.
Selective CO2uptake and vapor adsorption study within Sn(iv) porphyrin crystals
CrystEngComm, 2016, 18, 1515
7223981 CIFC72 H43 Co3 N6 O13R 3 224.811; 24.811; 21.455
90; 90; 120		11437.9Shen, Jian-Qiang; Wei, Yong-Sheng; Liao, Pei-Qin; Lin, Rui-Biao; Zhou, Dong-Dong; Zhang, Jie-Peng; Chen, Xiao-Ming
Unique (3,9)-connected porous coordination polymers constructed by tripodal ligands with bent arms
CrystEngComm, 2016, 18, 4115
7223982 CIFC72 H43 Co3 N6 O13R 320.186; 20.186; 20.2891
90; 90; 120		7159.7Shen, Jian-Qiang; Wei, Yong-Sheng; Liao, Pei-Qin; Lin, Rui-Biao; Zhou, Dong-Dong; Zhang, Jie-Peng; Chen, Xiao-Ming
Unique (3,9)-connected porous coordination polymers constructed by tripodal ligands with bent arms
CrystEngComm, 2016, 18, 4115
7223983 CIFC72 H43 Co3 N30 OR -3 c27.3444; 27.3444; 71.115
90; 90; 120		46050Shen, Jian-Qiang; Wei, Yong-Sheng; Liao, Pei-Qin; Lin, Rui-Biao; Zhou, Dong-Dong; Zhang, Jie-Peng; Chen, Xiao-Ming
Unique (3,9)-connected porous coordination polymers constructed by tripodal ligands with bent arms
CrystEngComm, 2016, 18, 4115
7223984 CIFC60 H24 N8 O8 Zn3I 4/m m m16.679; 16.679; 17.674
90; 90; 90		4916.7Sakuma, Takao; Sakai, Hayato; Araki, Yasuyuki; Wada, Takehiko; Hasobe, Taku
Control of local structures and photophysical properties of zinc porphyrin-based supramolecular assemblies structurally organized by regioselective ligand coordination.
Physical chemistry chemical physics : PCCP, 2016, 18, 5453-5463
7223985 CIFC10 F8P 1 21/c 113.3203; 4.8791; 19.8516
90; 100.245; 90		1269.61Dobrowolski, Michał A; Cyrański, Michał K; Wróbel, Zbigniew
Cyclic π-electron delocalization in non-planar linear acenes.
Physical chemistry chemical physics : PCCP, 2016, 18, 11813-11820
7223986 CIFC10 Cl8P 1 21/n 19.7244; 7.1739; 18.2816
90; 98.317; 90		1261.9Dobrowolski, Michał A; Cyrański, Michał K; Wróbel, Zbigniew
Cyclic π-electron delocalization in non-planar linear acenes.
Physical chemistry chemical physics : PCCP, 2016, 18, 11813-11820
7223987 CIFC10 Br8P b c n11.3832; 7.8114; 16.5506
90; 90; 90		1471.66Dobrowolski, Michał A; Cyrański, Michał K; Wróbel, Zbigniew
Cyclic π-electron delocalization in non-planar linear acenes.
Physical chemistry chemical physics : PCCP, 2016, 18, 11813-11820
7223988 CIFC14 Cl10P -17.1558; 9.5084; 12.4684
75.854; 82.701; 87.954		815.95Dobrowolski, Michał A; Cyrański, Michał K; Wróbel, Zbigniew
Cyclic π-electron delocalization in non-planar linear acenes.
Physical chemistry chemical physics : PCCP, 2016, 18, 11813-11820
7224001 CIFC94 H90 Mn8 N8 O28P -114.0134; 14.8016; 15.2457
105.689; 113.922; 103.178		2570Yang, Fei; Deng, Yong-Kai; Guo, Ling-Yu; Su, Hai-Feng; Jagličić, Zvonko; Feng, Zhen-Yu; Zhuang, Gui-Lin; Zeng, Su-Yuan; Sun, Di
Structural, electrochemical and magnetic analyses of a new octanuclear MnIII2MnII6cluster with linked-defect cubane topology
CrystEngComm, 2016, 18, 1329
7224002 CIFC7 H9 Cl Cu N2 SP 1 21/c 18.127; 15.764; 8.041
90; 111.816; 90		956.4Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224003 CIFC14 H18 Cl Cu N4 S2P -18.8605; 9.6615; 11.7506
66.423; 82.85; 78.316		901.79Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224004 CIFC14 H18 Br Cu N4 S2C 1 2/c 121.7441; 9.8378; 16.9298
90; 90.766; 90		3621.2Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224005 CIFC28 H36 Cu2 I2 N8 S4C 1 2/c 121.91; 9.9443; 16.891
90; 90.414; 90		3680.1Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224006 CIFC4 H7 Cl Cu N2 SP 1 21/n 17.9771; 10.673; 8.921
90; 97.182; 90		753.571Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224007 CIFC4 H10 Cu I N2 S2P -17.4292; 8.0762; 9.614
107.059; 90.971; 110.972		510.1Troyano, Javier; Perles, Josefina; Amo-Ochoa, Pilar; Zamora, Félix; Delgado, Salomé
Strong luminescent copper(i) halide coordination polymers and dinuclear complexes with thioacetamide and N,N′-donor ligands
CrystEngComm, 2016, 18, 1809
7224008 CIFC53 H42 N8 Ni O21 S3 U2P -113.8935; 14.0662; 18.2195
108.577; 110.263; 97.592		3046.3Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224009 CIFC38 H56 Cl Co N8 O26 S4 U2P 1 21 110.8016; 20.409; 12.8547
90; 105.973; 90		2724.41Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224010 CIFC128 H96 Fe2 N18 O44 S6 U5P -113.7311; 15.5105; 17.8862
68.574; 70.094; 76.948		3311.7Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224011 CIFC123 H87 N17 Ni2 O43 S6 U5P -113.7804; 15.5944; 18.0932
67.6388; 69.388; 76.7394		3345.09Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224012 CIFC30 H26 Ag2 N6 O17 S3 U2P 42/n m c26.1007; 26.1007; 6.695
90; 90; 90		4560.95Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224013 CIFC136 H104 Ag5 N21 O41 S6 U4P 21 21 2118.4849; 26.8834; 31.5917
90; 90; 90		15699.1Thuéry, Pierre; Harrowfield, Jack
Counter-ion control of structure in uranyl ion complexes with 2,5-thiophenedicarboxylate
CrystEngComm, 2016, 18, 1550
7224021 CIFC28 H26 K O15 TbP 4/n n c15.513; 15.513; 26.445
90; 90; 90		6364.1Li, Yun; Wang, Ning; Huang, Jie-Yi; Zhang, Fei-Hua; Xiong, Yan-Ju; Cheng, Qian; Fang, Jie-Fang; Zhu, Fei-Fei; Long, Yi; Yue, Shan-Tang
KI-induced synthesis of highly connected 3D KI‒LnIIIheterobimetallic MOFs: temperature-dependent structure and physical properties
CrystEngComm, 2016, 18, 1570
7224022 CIFC28 H26 Dy K O15P 4/n n c15.322; 15.322; 26.327
90; 90; 90		6180.6Li, Yun; Wang, Ning; Huang, Jie-Yi; Zhang, Fei-Hua; Xiong, Yan-Ju; Cheng, Qian; Fang, Jie-Fang; Zhu, Fei-Fei; Long, Yi; Yue, Shan-Tang
KI-induced synthesis of highly connected 3D KI‒LnIIIheterobimetallic MOFs: temperature-dependent structure and physical properties
CrystEngComm, 2016, 18, 1570
7224023 CIFC59 H39 K O28 Tb3P n m a20.15; 30.14; 11.69
90; 90; 90		7100Li, Yun; Wang, Ning; Huang, Jie-Yi; Zhang, Fei-Hua; Xiong, Yan-Ju; Cheng, Qian; Fang, Jie-Fang; Zhu, Fei-Fei; Long, Yi; Yue, Shan-Tang
KI-induced synthesis of highly connected 3D KI‒LnIIIheterobimetallic MOFs: temperature-dependent structure and physical properties
CrystEngComm, 2016, 18, 1570
7224024 CIFC59 H39 Dy3 K O28P n m a19.1; 28.26; 11.1446
90; 90; 90		6015.5Li, Yun; Wang, Ning; Huang, Jie-Yi; Zhang, Fei-Hua; Xiong, Yan-Ju; Cheng, Qian; Fang, Jie-Fang; Zhu, Fei-Fei; Long, Yi; Yue, Shan-Tang
KI-induced synthesis of highly connected 3D KI‒LnIIIheterobimetallic MOFs: temperature-dependent structure and physical properties
CrystEngComm, 2016, 18, 1570
7224025 CIFC24 H18 N4 O2P -18.2616; 11.0442; 11.8712
69.313; 76.743; 71.691		953.45Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224026 CIFC21 H26 Cl4 N4 O3 SnP 1 21/c 18.3486; 27.473; 11.3936
90; 93.665; 90		2607.9Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224027 CIFC49 H42 Cl2 Cu2 N8 O15P n n a15.2508; 23.2887; 12.9853
90; 90; 90		4612Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224028 CIFC38 H40 Cl4 Mn2 N8 O4P -19.441; 10.9557; 10.9598
64.848; 88.44; 72.81		973.92Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224029 CIFC38 H32 Cl Fe N10 O2C 1 2/c 113.163; 19.772; 13.268
90; 92.198; 90		3450.6Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224030 CIFC52 H38 Fe2 N10 O5P -113.0767; 13.4441; 14.3843
100.563; 107.325; 98.963		2312.8Gumbau-Brisa, R.; Hayward, J. J.; Wallis, J. D.; Rawson, J. M.; Pilkington, M.
Structural insights into the coordination chemistry and reactivity of a 3,3′-bis-imine-2,2′-bipyridine ligand
CrystEngComm, 2016, 18, 1892
7224040 CIFC6 H16 B2 F8 N2 OP c a 2113.0629; 7.837; 11.6838
90; 90; 90		1196.12Han, Xiang-Bin; Hu, Pan; Shi, Chao; Zhang, Wen
1,4-Diazabicyclo[2.2.2]octane-based disalts showing non-centrosymmetric structures and phase transition behaviors
CrystEngComm, 2016, 18, 1563
7224041 CIFC6 H16 B2 F8 N2 OP c a 2113.231; 7.883; 11.786
90; 90; 90		1229.3Han, Xiang-Bin; Hu, Pan; Shi, Chao; Zhang, Wen
1,4-Diazabicyclo[2.2.2]octane-based disalts showing non-centrosymmetric structures and phase transition behaviors
CrystEngComm, 2016, 18, 1563
7224042 CIFC6 H16 Cl2 N2 O9P c a 2113.357; 8.073; 11.836
90; 90; 90		1276.3Han, Xiang-Bin; Hu, Pan; Shi, Chao; Zhang, Wen
1,4-Diazabicyclo[2.2.2]octane-based disalts showing non-centrosymmetric structures and phase transition behaviors
CrystEngComm, 2016, 18, 1563
7224043 CIFC6 H16 Cl2 N2 O9P c a 2113.296; 8.069; 11.772
90; 90; 90		1263Han, Xiang-Bin; Hu, Pan; Shi, Chao; Zhang, Wen
1,4-Diazabicyclo[2.2.2]octane-based disalts showing non-centrosymmetric structures and phase transition behaviors
CrystEngComm, 2016, 18, 1563
7224044 CIFC72 H60 Cl4 Mn O4 P4 ZnF d d 220.7414; 32.981; 9.7539
90; 90; 90		6672.4Liu, Xiaolong; Wang, Guangqiang; Dang, Yangyang; Zhang, Shaojun; Tian, Hanlin; Ren, Yan; Tao, Xutang
A new potential nonlinear optical hybrid semi-organic crystal of ZnMnCl4(TPPO)4with attractive physical properties
CrystEngComm, 2016, 18, 1818
7224045 CIFC36 H30 Cl2 O2 P2 ZnF d d 220.718; 33.018; 9.751
90; 90; 90		6670Liu, Xiaolong; Wang, Guangqiang; Dang, Yangyang; Zhang, Shaojun; Tian, Hanlin; Ren, Yan; Tao, Xutang
A new potential nonlinear optical hybrid semi-organic crystal of ZnMnCl4(TPPO)4with attractive physical properties
CrystEngComm, 2016, 18, 1818
7224048 CIFC13 H11 Co N O6P 1 21/c 113.876; 12.212; 7.7376
90; 104.205; 90		1271.1Hou, Juan-Juan; Li, Xiao-Qing; Tian, Bao-Qiang; Zhang, Xian-Ming
Genuine supramolecular isomers based on Y-shaped pyridinedicarboxylate ligands with distinct topology: 2D 63layer, kgd layer to 3D rtl net
CrystEngComm, 2016, 18, 2065
7224049 CIFC13 H11 Co N O6P -16.4032; 7.7936; 12.7782
74.095; 83.775; 84.04		607.82Hou, Juan-Juan; Li, Xiao-Qing; Tian, Bao-Qiang; Zhang, Xian-Ming
Genuine supramolecular isomers based on Y-shaped pyridinedicarboxylate ligands with distinct topology: 2D 63layer, kgd layer to 3D rtl net
CrystEngComm, 2016, 18, 2065
7224050 CIFC13 H11 Co N O6P -16.4023; 16.0344; 25.698
106.588; 96.084; 92.993		2504.62Hou, Juan-Juan; Li, Xiao-Qing; Tian, Bao-Qiang; Zhang, Xian-Ming
Genuine supramolecular isomers based on Y-shaped pyridinedicarboxylate ligands with distinct topology: 2D 63layer, kgd layer to 3D rtl net
CrystEngComm, 2016, 18, 2065
7224059 CIFC12 H13 N O7C 1 2/c 128.77; 8.771; 10.211
90; 108.17; 90		2448Singh, Shiv Shankar; Vasantha, K. Y.; Sattur, A. P.; Thakur, Tejender S.
Experimental and computational crystal structure landscape study of nigerloxin: a fungal metabolite from Aspergillus niger
CrystEngComm, 2016, 18, 1740
7224060 CIFC10 H9 N O6P 1 21/c 111.277; 8.788; 9.851
90; 96.003; 90		970.9Singh, Shiv Shankar; Vasantha, K. Y.; Sattur, A. P.; Thakur, Tejender S.
Experimental and computational crystal structure landscape study of nigerloxin: a fungal metabolite from Aspergillus niger
CrystEngComm, 2016, 18, 1740
7224061 CIFC20 H22 OP -18.4061; 8.6026; 12.582
91.647; 102.618; 112.149		816.1Wang, Kuai; Meng, Ling-Guo; Zhang, Qi; Wang, Lei
Direct construction of 4-aryl tetralones via visible-light-induced cyclization of styrenes with molecular oxygen
Green Chem., 2016, 18, 2864
7224069 CIFC216 H212 Cl4 Co16 F4 N4 O44 S16C 1 2/c 142.6717; 26.3547; 33.6116
90; 113.576; 90		34644.5Hang, Xinxin; Wang, Shentang; Zhu, Xiaofei; Han, Haitao; Liao, Wuping
pH-dependent formation of different coordination cages based on Co4-TC4A secondary building units and bridging ligands
CrystEngComm, 2016, 18, 4938
7224070 CIFC264 H224 Cl4 Co16 F8 N8 O48 S16I 4/m30.146; 30.146; 21.5634
90; 90; 90		19596.4Hang, Xinxin; Wang, Shentang; Zhu, Xiaofei; Han, Haitao; Liao, Wuping
pH-dependent formation of different coordination cages based on Co4-TC4A secondary building units and bridging ligands
CrystEngComm, 2016, 18, 4938
7224071 CIFC216 H216 Cl4 Co16 N4 O44 S16C 1 2/c 142.516; 28.4143; 33.6347
90; 111.972; 90		37682Hang, Xinxin; Wang, Shentang; Zhu, Xiaofei; Han, Haitao; Liao, Wuping
pH-dependent formation of different coordination cages based on Co4-TC4A secondary building units and bridging ligands
CrystEngComm, 2016, 18, 4938
7224072 CIFC264 H232 Cl4 Co16 N8 O48 S16I 4/m30.163; 30.163; 21.6122
90; 90; 90		19662.9Hang, Xinxin; Wang, Shentang; Zhu, Xiaofei; Han, Haitao; Liao, Wuping
pH-dependent formation of different coordination cages based on Co4-TC4A secondary building units and bridging ligands
CrystEngComm, 2016, 18, 4938
7224073 CIFC168 H432 Cl18 La12 N24 Ni15 O276P m -3 m21.0408; 21.0408; 21.0408
90; 90; 90		9315.1Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224074 CIFC168 H460 Cl18 Gd12 N24 Ni15 O290P m -3 m20.9271; 20.9271; 20.9271
90; 90; 90		9164.9Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224075 CIFC14 H30 Cl La N2 Ni O21P 1 21/c 118.7646; 9.0729; 18.6765
90; 116.804; 90		2838.02Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224076 CIFC14 H36 Cl N2 Nd Ni O21P 1 21/c 118.633; 8.9756; 18.637
90; 116.699; 90		2784.6Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224077 CIFC28 H68 N6 Nd2 Ni2 O38P -19.2011; 12.234; 12.51
85.62; 80.05; 68.91		1294Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224078 CIFC28 H36 Dy2 N6 Ni2 O38P -19.1672; 12.17; 12.442
85.92; 79.65; 68.68		1272Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224079 CIFC14 H34 Cl Dy N2 Ni O16P -17.558; 11.269; 15.561
100.694; 103.838; 105.732		1193.4Zhang, Han; Yan, Zhi-Hao; Luo, Yun; Zheng, Xiu-Ying; Kong, Xiang-Jian; Long, La-Sheng; Zheng, Lan-Sun
Anion-controlled assembly of a series of heterometallic 3d‒4f compounds with 0D cluster, 1D chain, 2D network and 3D frameworks
CrystEngComm, 2016, 18, 4142
7224080 CIFC21 H19 Eu N7 O9C 1 2/c 128.11; 13.7799; 14.3362
90; 100.267; 90		5464.3Wu, Lan-Lan; Zhao, Junfang; Wang, Hui; Wang, Jingyuan
A lanthanide(iii) metal‒organic framework exhibiting ratiometric luminescent temperature sensing and tunable white light emission
CrystEngComm, 2016, 18, 4268
7224081 CIFC21 H19 N7 O9 TbC 1 2/c 128.282; 13.564; 14.509
90; 100.155; 90		5478.7Wu, Lan-Lan; Zhao, Junfang; Wang, Hui; Wang, Jingyuan
A lanthanide(iii) metal‒organic framework exhibiting ratiometric luminescent temperature sensing and tunable white light emission
CrystEngComm, 2016, 18, 4268
7224082 CIFB3 Na2 O8 SbP 1 21/c 15.8278; 10.3521; 10.4775
90; 102.948; 90		616.04Yan, Dong; Hu, Chun-Li; Mao, Jiang-Gao
A2SbB3O8(A = Na, K, Rb) and β-RbSbB2O6: two types of alkali boroantimonates with 3D anionic architectures composed of SbO6octahedra and borate groups
CrystEngComm, 2016, 18, 1655
7224083 CIFB3 K2 O8 SbP 1 21/c 15.9013; 11.0876; 10.9497
90; 103.218; 90		697.47Yan, Dong; Hu, Chun-Li; Mao, Jiang-Gao
A2SbB3O8(A = Na, K, Rb) and β-RbSbB2O6: two types of alkali boroantimonates with 3D anionic architectures composed of SbO6octahedra and borate groups
CrystEngComm, 2016, 18, 1655
7224084 CIFB3 O8 Rb2 SbP 1 21/c 15.9381; 11.2928; 11.3181
90; 103.754; 90		737.2Yan, Dong; Hu, Chun-Li; Mao, Jiang-Gao
A2SbB3O8(A = Na, K, Rb) and β-RbSbB2O6: two types of alkali boroantimonates with 3D anionic architectures composed of SbO6octahedra and borate groups
CrystEngComm, 2016, 18, 1655
7224085 CIFB2 O6 Rb SbC 1 c 111.7148; 7.1633; 7.4109
90; 125.435; 90		506.71Yan, Dong; Hu, Chun-Li; Mao, Jiang-Gao
A2SbB3O8(A = Na, K, Rb) and β-RbSbB2O6: two types of alkali boroantimonates with 3D anionic architectures composed of SbO6octahedra and borate groups
CrystEngComm, 2016, 18, 1655
7224086 CIFC54 H42 Co7 N6 O35C m c e24.6165; 35.8569; 30.2783
90; 90; 90		26725.8Guo, Xiao-Qing; Wang, Miao; Tang, Yan-Feng; Meng, Fei; Jiang, Guo-Qing; Zhu, Jin-Li
A new Co-nitroimidazolate‒dicarboxylate pillared-layer network with various types of channels and ultra-large cages for gas uptake
CrystEngComm, 2016, 18, 1768
7224087 CIFC8 H14 O12 ZnP -15.1749; 7.2736; 9.1901
108.304; 105.213; 92.434		313.95Ruggiero, Michael T.; Korter, Timothy M.
The crucial role of water in shaping low-barrier hydrogen bonds.
Physical chemistry chemical physics : PCCP, 2016, 18, 5521-5528
7224088 CIFC8 H14 Ni O12P -15.142; 7.2793; 9.1121
108.025; 105.191; 92.14		310.38Ruggiero, Michael T.; Korter, Timothy M.
The crucial role of water in shaping low-barrier hydrogen bonds.
Physical chemistry chemical physics : PCCP, 2016, 18, 5521-5528
7224089 CIFC8 H14 Co O12P -15.1742; 7.2742; 9.2053
108.809; 105.003; 92.409		313.79Ruggiero, Michael T.; Korter, Timothy M.
The crucial role of water in shaping low-barrier hydrogen bonds.
Physical chemistry chemical physics : PCCP, 2016, 18, 5521-5528
7224090 CIFC8 H14 Fe O12P -15.2115; 7.3307; 9.2529
109.019; 105.339; 92.53		318.98Ruggiero, Michael T.; Korter, Timothy M.
The crucial role of water in shaping low-barrier hydrogen bonds.
Physical chemistry chemical physics : PCCP, 2016, 18, 5521-5528
7224091 CIFC8 H14 Mn O12P -15.2823; 7.3398; 9.3651
109.765; 105.152; 92.454		326.37Ruggiero, Michael T.; Korter, Timothy M.
The crucial role of water in shaping low-barrier hydrogen bonds.
Physical chemistry chemical physics : PCCP, 2016, 18, 5521-5528
7224101 CIFC40 H38 Dy F21 N2 O6P 1 21/c 113.6094; 20.4337; 17.9312
90; 108.986; 90		4715.2Gao, Chen; Yang, Qian; Wang, Bing-Wu; Wang, Zhe-Ming; Gao, Song
Evaporable lanthanide single-ion magnet
CrystEngComm, 2016, 18, 4165
7224102 CIFC42 H38 Dy F21 N2 O6P 1 21/c 114.0899; 19.8329; 17.4263
90; 102.091; 90		4761.64Gao, Chen; Yang, Qian; Wang, Bing-Wu; Wang, Zhe-Ming; Gao, Song
Evaporable lanthanide single-ion magnet
CrystEngComm, 2016, 18, 4165
7224103 CIFC32 H12 Br4 O16 Zn3P b c a20.892; 24.47; 25.238
90; 90; 90		12902Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224104 CIFC28 H18 Br2 N2 O8 Zn2C 2 2 2114.0217; 31.3444; 27.9952
90; 90; 90		12303.9Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224105 CIFC64 H24 N8 O62 Zn13P -112.882; 14.292; 16.936
110.255; 99.167; 106.39		2690Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224106 CIFC28 H22 N4 O14 Zn2P 1 21/c 112.5013; 14.5412; 8.2241
90; 104.849; 90		1445.08Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224107 CIFC16 H16 Cd N3 O8P -18.5151; 10.0658; 11.9929
67.113; 88.027; 76.771		920.16Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224108 CIFC15 H11 N O4 ZnI 41 2 29.946; 9.946; 31.544
90; 90; 90		3120Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224109 CIFC28 H36 N4 O12 Zn2P 1 21 19.919; 16.851; 10.145
90; 93.18; 90		1693.1Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224110 CIFC28 H22 N2 O8 ZnC 1 2/c 120.941; 8.9021; 15.065
90; 117.91; 90		2481.7Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224111 CIFC15 H14 N O5 ZnP -18.2249; 9.8672; 11.221
68.441; 68.947; 66.741		753.3Ma, De-Yun; Qin, Liang; Lei, Jia-Mei; Liang, Yun-Qiu; Lin, Wei-Jie; Yan, Jing-Jing; Ding, Wan-Qiu; Guo, Hai-Fu; Ling, Yun
Structural diversity of a series of coordination polymers built from 5-substituted isophthalic acid with or without a methyl-functionalized N-donor ligand
CrystEngComm, 2016, 18, 1363
7224112 CIFC8 H37 Cu4 N8 Na0 Nb3 O22 W3P n n m11.2042; 14.7102; 9.5638
90; 90; 90		1576.3Jin, Lu; Li, Xin-Xiong; Zhao, Dan; Li, Hao-Hong; Zheng, Shou-Tian
A rare polyniobotungstate-based framework and its structural transformation in a single-crystal-to-single-crystal process induced by iodide ions
CrystEngComm, 2016, 18, 1705
7224113 CIFC14 H14 N2 O2P 1 21 17.5292; 5.7936; 13.9668
90; 93.766; 90		607.93Chaudhary, Priyanka; Gupta, Surabhi; Muniyappan, Nalluchamy; Sabiah, Shahulhameed; Kandasamy, Jeyakumar
An efficient synthesis of N-nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite
Green Chem., 2016, 18, 2323
7224120 CIFC108 H150 Ag6 N30 O21I 4124.5154; 24.5154; 76.118
90; 90; 90		45747Abu-Youssef, M. A. M.; Soliman, S. M.; Sharaf, M. M.; Albering, J. H.; Öhrström, L.
Topology analysis reveals supramolecular organisation of 96 large complex ions into one geometrical object
CrystEngComm, 2016, 18, 1883
7224121 CIFC9 H12 N2P b c a10.4951; 8.104; 18.3689
90; 90; 90		1562.32Abu-Youssef, M. A. M.; Soliman, S. M.; Sharaf, M. M.; Albering, J. H.; Öhrström, L.
Topology analysis reveals supramolecular organisation of 96 large complex ions into one geometrical object
CrystEngComm, 2016, 18, 1883
7224122 CIFC18 H24 Ag Cl N4 O4P 1 21/c 111.3787; 8.1171; 21.41
90; 95.969; 90		1966.8Abu-Youssef, M. A. M.; Soliman, S. M.; Sharaf, M. M.; Albering, J. H.; Öhrström, L.
Topology analysis reveals supramolecular organisation of 96 large complex ions into one geometrical object
CrystEngComm, 2016, 18, 1883
7224123 CIFC32 H33 B2 Co F8 N11P n m a14.582; 22.199; 11.3662
90; 90; 90		3679.3Shao, Dong; Shi, Le; Zhang, Shao-Liang; Zhao, Xin-Hua; Wu, Dong-Qing; Wei, Xiao-Qin; Wang, Xin-Yi
Syntheses, structures, and magnetic properties of three new chain compounds based on a pentagonal bipyramidal Co(ii) building block
CrystEngComm, 2016, 18, 4150
7224124 CIFC41 H41.99 B2 Co F8 N12P -113.8571; 16.6586; 19.6933
68.138; 88.062; 88.016		4215.5Shao, Dong; Shi, Le; Zhang, Shao-Liang; Zhao, Xin-Hua; Wu, Dong-Qing; Wei, Xiao-Qin; Wang, Xin-Yi
Syntheses, structures, and magnetic properties of three new chain compounds based on a pentagonal bipyramidal Co(ii) building block
CrystEngComm, 2016, 18, 4150
7224125 CIFC29 H30 B2 Co F8 N10 OP -19.7431; 12.2307; 14.5005
95.953; 107.564; 99.913		1600.4Shao, Dong; Shi, Le; Zhang, Shao-Liang; Zhao, Xin-Hua; Wu, Dong-Qing; Wei, Xiao-Qin; Wang, Xin-Yi
Syntheses, structures, and magnetic properties of three new chain compounds based on a pentagonal bipyramidal Co(ii) building block
CrystEngComm, 2016, 18, 4150
7224126 CIFC27 H20 N2 O6 ZnP -19.415; 10.117; 14.657
85.815; 74.704; 70.067		1265.7Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224127 CIFC27 H20 N2 O6 ZnP -111.106; 15.856; 17.853
82.222; 88.158; 88.201		3112.2Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224128 CIFC35 H33 N5 O7 ZnP b c a10.972; 16.101; 37.978
90; 90; 90		6709Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224129 CIFC30 H29 Cd N3 O8P -19.502; 11.646; 13.277
84.836; 73.449; 84.18		1398.2Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224130 CIFC27 H20 Co N2 O6C 1 2/m 19.5536; 28.335; 10.1074
90; 107.415; 90		2610.7Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224131 CIFC66 H54 Co3 N8 O18P 1 21/c 113.1143; 18.2637; 18.1148
90; 91.971; 90		4336.2Pal, Sanchari; Pal, Tapan K.; Bharadwaj, Parimal K.
Solvothermal synthesis of coordination polymers at different temperatures and their luminescence studies
CrystEngComm, 2016, 18, 1825
7224132 CIFC36 H50 O6 S2P 1 21/a 114.1458; 7.2193; 17.4712
90; 98.5591; 90		1764.34Bowen, Alice M.; Jones, Michael W.; Lovett, Janet E.; Gaule, Thembanikosi G.; McPherson, Michael J.; Dilworth, Jonathan R.; Timmel, Christiane R.; Harmer, Jeffrey R.
Exploiting orientation-selective DEER: determining molecular structure in systems containing Cu(ii) centres.
Physical chemistry chemical physics : PCCP, 2016, 18, 5981-5994
7224138 CIFAl Li3 O5 SiP n a 215.331; 15.551; 4.782
90; 90; 90		396.4Chen, Xinglong; Zhang, Fangfang; Liu, Lili; Lei, Bing-Hua; Dong, Xiaoyu; Yang, Zhihua; Li, Hongyi; Pan, Shilie
Li3AlSiO5: the first aluminosilicate as a potential deep-ultraviolet nonlinear optical crystal with the quaternary diamond-like structure.
Physical chemistry chemical physics : PCCP, 2016, 18, 4362-4369
7224152 CIFC5 H13 Cl N6 S2C m c m14.75; 9.887; 8.419
90; 90; 90		1227.8Liu, Yu-Ling; Wang, Yu-Feng; Zhang, Wen
Switchable dielectric constant in an inclusion compound bis(thiourea) imidazolium chloride
CrystEngComm, 2016, 18, 1958
7224153 CIFC5 H13 Cl N6 S2P 21 21 2114.674; 9.779; 8.412
90; 90; 90		1207.1Liu, Yu-Ling; Wang, Yu-Feng; Zhang, Wen
Switchable dielectric constant in an inclusion compound bis(thiourea) imidazolium chloride
CrystEngComm, 2016, 18, 1958
7224154 CIFC5 H13 Cl N6 S2C 2 2 2114.7; 9.771; 8.414
90; 90; 90		1208.5Liu, Yu-Ling; Wang, Yu-Feng; Zhang, Wen
Switchable dielectric constant in an inclusion compound bis(thiourea) imidazolium chloride
CrystEngComm, 2016, 18, 1958
7224155 CIFC50 H34 Cu4 N4 O15P 1 21/c 17.48; 23.63; 12.47
90; 98.05; 90		2182.4Song, Yang; Fan, Rui-Qing; Wang, Xin-Ming; Gao, Song; Du, Xi; Wang, Ping; Yang, Yu-Lin
Direct observation of a fast single-crystal-to-single-crystal transformation from a CuII-framework to a CuI-chain mediated by ascorbic acid
CrystEngComm, 2016, 18, 1878
7224156 CIFC50 H34 Cu2 N4 O14P -17.8383; 9.4782; 14.9216
91.826; 95.897; 103.056		1072.46Song, Yang; Fan, Rui-Qing; Wang, Xin-Ming; Gao, Song; Du, Xi; Wang, Ping; Yang, Yu-Lin
Direct observation of a fast single-crystal-to-single-crystal transformation from a CuII-framework to a CuI-chain mediated by ascorbic acid
CrystEngComm, 2016, 18, 1878
7224157 CIFC56 H100 N4 O21 V6P 1 21/c 111.598; 19.518; 15.301
90; 91.47; 90		3462.5Bayaguud, Aruuhan; Chen, Kun; Wei, Yongge
Facile synthesis of an organically-derivatized hexavanadate containing the remote amino group, TBA2[V6O13{(OCH2)3CNH2}2]
CrystEngComm, 2016, 18, 4042
7224158 CIFC8 H26 N2 O23 V6C 1 2/m 110.381; 12.311; 9.6175
90; 104.2; 90		1191.6Bayaguud, Aruuhan; Chen, Kun; Wei, Yongge
Facile synthesis of an organically-derivatized hexavanadate containing the remote amino group, TBA2[V6O13{(OCH2)3CNH2}2]
CrystEngComm, 2016, 18, 4042
7224168 CIFC67 H56 N11 O35 Zn4C 1 2/c 125.151; 10.4057; 30.589
90; 113.035; 90		7367.2Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224169 CIFC72 H50 N12 Ni3 O28C 1 2/c 121.687; 18.249; 22.474
90; 118.15; 90		7842Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224170 CIFC24 H14 N4 Ni O8.02C 1 2/c 113.5739; 19.361; 8.7636
90; 96.151; 90		2289.9Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224171 CIFC24 H14 Mn N4 O8C 1 2/c 113.827; 19.685; 8.9064
90; 97.32; 90		2404.4Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224172 CIFC12 H7 Co0.5 N2 O4.18C 1 2/c 113.641; 19.536; 8.806
90; 96.639; 90		2331Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224173 CIFC24 H32 N4 Ni O17P 21 21 217.361; 15.645; 26.957
90; 90; 90		3104.4Chen, Li-Zhuang; Pan, Qi-Jian; Cao, Xing-Xing; Wang, Fang-Ming
Crystal structure, magnetism, and dielectric properties based on the axially chiral ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid
CrystEngComm, 2016, 18, 1944
7224174 CIFC22 H40 N14 S4P -17.9939; 9.0331; 11.1337
89.976; 83.248; 85.245		795.6Taouss, Christina; Döring, Cindy; Jones, Peter G.; Pinkert, Lukas; Strey, Mark
Single crystals that spontaneously spawn other single crystals: a ternary and a binary adduct of thiourea and 2,5-dimethylpyrazine
CrystEngComm, 2016, 18, 1842
7224175 CIFC8 H16 N4 O SP -18.3895; 9.1961; 15.9849
103.892; 97.021; 90.97		1186.83Taouss, Christina; Döring, Cindy; Jones, Peter G.; Pinkert, Lukas; Strey, Mark
Single crystals that spontaneously spawn other single crystals: a ternary and a binary adduct of thiourea and 2,5-dimethylpyrazine
CrystEngComm, 2016, 18, 1842
7224176 CIFC19 H34 N14 S4P -17.7966; 9.0094; 10.8792
89.053; 85.454; 83.906		757.45Taouss, Christina; Döring, Cindy; Jones, Peter G.; Pinkert, Lukas; Strey, Mark
Single crystals that spontaneously spawn other single crystals: a ternary and a binary adduct of thiourea and 2,5-dimethylpyrazine
CrystEngComm, 2016, 18, 1842
7224177 CIFC12 H8 Cl2 I N2 O2 RuP -16.6617; 9.4643; 13.0807
70.44; 80.953; 83.307		765.64Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224178 CIFC13 H9 Br2 Cl3 I4 N2 O2 RuP 1 21 16.6553; 16.3426; 10.2145
90; 97.865; 90		1100.53Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224179 CIFC12 H8 I6 N2 O2 RuP 21 21 215.6811; 7.3656; 9.4737
90; 90; 90		1094.22Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224180 CIFC12 H8 I4 N2 O2 RuP -19.0961; 10.371; 10.572
112.39; 93.49; 90.7		919.7Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224181 CIFC13 H9 Br Cl3 I3 N2 O2 RuP 1 21/n 111.6841; 11.4179; 17.2077
90; 105.946; 90		2207.3Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224182 CIFC13 H10 Cl4 N2 O2 RuP -16.4683; 12.3842; 21.1414
89.106; 83.451; 87.535		1680.82Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224183 CIFC12 H8 Br2 N2 O2 RuP 1 n 18.3627; 6.9269; 12.705
90; 103.49; 90		715.67Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224184 CIFC12 H8 I2 N2 O2 RuP b c a13.7231; 11.922; 18.0712
90; 90; 90		2956.6Ding, Xin; Tuikka, Matti J.; Hirva, Pipsa; Kukushkin, Vadim Yu.; Novikov, Alexander S.; Haukka, Matti
Fine-tuning halogen bonding properties of diiodine through halogen‒halogen charge transfer ‒ extended [Ru(2,2′-bipyridine)(CO)2X2]·I2systems (X = Cl, Br, I)
CrystEngComm, 2016, 18, 1987
7224185 CIFC18 H24 N6 O6P 1 21/c 116.2; 7.378; 8.793
90; 105.079; 90		1014.8Sarceviča, I.; Kons, A.; Orola, L.
Isoniazid cocrystallisation with dicarboxylic acids: vapochemical, mechanochemical and thermal methods
CrystEngComm, 2016, 18, 1625
7224194 CIFC135 H202 Ag4 Cl6 F12 O34 S12P -118.1183; 19.5986; 24.7135
75.385; 83.625; 74.064		8157.1Helttunen, Kaisa; Nissinen, Maija
Inverted molecular cups: 1-D and 2-D Ag(i) coordination polymers from resorcinarene bis-thiacrowns
CrystEngComm, 2016, 18, 4944
7224195 CIFC72 H107 Ag3 F9 O19.5 S6P -114.4639; 17.1573; 19.8936
67.754; 71.544; 88.853		4306.2Helttunen, Kaisa; Nissinen, Maija
Inverted molecular cups: 1-D and 2-D Ag(i) coordination polymers from resorcinarene bis-thiacrowns
CrystEngComm, 2016, 18, 4944
7224196 CIFC79 H111 Ag4.5 F13.5 O20.5 S6P 1 21/n 114.9657; 31.1456; 22.3769
90; 94.729; 90		10394.7Helttunen, Kaisa; Nissinen, Maija
Inverted molecular cups: 1-D and 2-D Ag(i) coordination polymers from resorcinarene bis-thiacrowns
CrystEngComm, 2016, 18, 4944
7224197 CIFC153 H227 Ag5 F15 O32.5 S8P -117.7963; 20.7997; 24.3087
92.255; 98.785; 106.258		8504.9Helttunen, Kaisa; Nissinen, Maija
Inverted molecular cups: 1-D and 2-D Ag(i) coordination polymers from resorcinarene bis-thiacrowns
CrystEngComm, 2016, 18, 4944
7224206 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5457; 13.4021; 29.7173
90; 95.335; 90		4578.4Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224207 CIFC48 H73 B N4 O3 PdP 1 21/n 111.4775; 13.3647; 29.9849
90; 94.569; 90		4584.9Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224208 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5673; 13.4937; 30.088
90; 93.738; 90		4686.3Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224209 CIFC48 H73 B N4 O3 PdP 1 21/n 111.583; 13.5168; 30.1137
90; 93.57; 90		4705.6Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224210 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5844; 13.5468; 30.1451
90; 93.333; 90		4722.7Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224211 CIFC48 H73 B N4 O3 PdP 1 21/n 111.6183; 13.554; 30.111
90; 93.455; 90		4733.1Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224212 CIFC48 H73 B N4 O3 PdP 1 21/n 111.65; 13.5543; 30.068
90; 93.859; 90		4737.2Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224213 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5238; 13.4068; 29.8526
90; 95.231; 90		4592.9Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224214 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5241; 13.4062; 29.8989
90; 95.061; 90		4601.2Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224215 CIFC48 H73 B N4 O3 PdP 1 21/n 111.4898; 13.3882; 29.98
90; 94.753; 90		4595.9Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224216 CIFC48 H73 B N4 O3 PdP 1 21/n 111.4937; 13.381; 29.9575
90; 94.717; 90		4591.8Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224217 CIFC48 H73 B N4 O3 PdP 1 21/n 111.4854; 13.3693; 30.0108
90; 94.639; 90		4593.1Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224218 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5322; 13.4261; 30.0361
90; 94.162; 90		4638.3Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224219 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5569; 13.4632; 30.0545
90; 93.906; 90		4665.4Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224220 CIFC48 H73 B N4 O3 PdP 1 21/n 111.5703; 13.4876; 30.0621
90; 93.739; 90		4681.4Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224221 CIFC48 H73 B N4 O3 PdP 1 21/n 111.6115; 13.5033; 29.982
90; 93.955; 90		4689.8Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224222 CIFC48 H73 B N4 O3 PdP 1 21/n 111.646; 13.5277; 30.0138
90; 93.953; 90		4717.2Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224223 CIFC48 H73 B N4 O3 PdP 1 21/n 111.6422; 13.5412; 30.0467
90; 93.985; 90		4725.4Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224224 CIFC48 H73 B N4 O3 PdP 1 21/n 111.6538; 13.5552; 30.0383
90; 93.725; 90		4735.1Hatcher, Lauren E.
Raising the (metastable) bar: 100% photo-switching in [Pd(Bu4dien)(η1-N̲O2)]+approaches ambient temperature
CrystEngComm, 2016, 18, 4180
7224225 CIFC30 H52 N6 O17C 1 2/c 113.691; 22.544; 11.572
90; 96.98; 90		3545.2Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224226 CIFC30 H45 Mn N6 Na O21P 1 21/c 111.73; 19.81; 17.13
90; 105.77; 90		3830.7Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224227 CIFC30 H38 N6 Ni O11C 1 2/c 118.78; 18.11; 9.2
90; 106.22; 90		3004.4Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224228 CIFC30 H40 N6 O14 Zn2P 1 21/n 110.83; 18.48; 16.55
90; 103.9; 90		3215Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224229 CIFC30 H50 N6 Ni O19 ZnP 1 21/n 111.36; 22.08; 15.56
90; 90.2; 90		3902.9Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224230 CIFC30 H52 Mn N6 O20 ZnC 1 2/c 137; 12.5; 18.68
90; 111.4; 90		8044Aríñez-Soriano, J.; Albalad, J.; Pérez-Carvajal, J.; Imaz, I.; Busqué, F.; Juanhuix, J.; Maspoch, D.
Two-step synthesis of heterometallic coordination polymers using a polyazamacrocyclic linker
CrystEngComm, 2016, 18, 4196
7224231 CIFC13 H15 N O8P -14.9477; 10.5762; 13.8911
109.507; 95.486; 101.807		660Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224232 CIFC11 H13 N O8P 1 21/c 14.7352; 16.3413; 15.6208
90; 91.454; 90		1208.34Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224233 CIFC11 H12 N O7.5P -18.0698; 10.3449; 15.3908
102.993; 91.11; 109.434		1174.4Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224234 CIFC15 H17 N2 O9.5P -111.4899; 13.1674; 13.3084
67.527; 67.492; 64.74		1623.5Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224235 CIFC12.5 H14 N O7.5P -18.2761; 11.6893; 14.7645
108.269; 97.664; 101.744		1297.75Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224236 CIFC37 H39 N3 O23P -19.1318; 14.0453; 15.5062
79.362; 85.337; 79.211		1917.82Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224237 CIFC13 H15 N O7.5P 15.927; 8.342; 13.899
79.829; 84.029; 77.411		658.6Kaur, Ramanpreet; Cherukuvada, Suryanarayan; Managutti, Praveen B.; Row, Tayur N. Guru
A gallic acid‒succinimide co-crystal landscape: polymorphism, pseudopolymorphism, variable stoichiometry co-crystals and concomitant growth of non-solvated and solvated co-crystals
CrystEngComm, 2016, 18, 3191
7224244 CIFC144 H72 Cl3 Ir3 N12 O64 Zr12I m -3 m38.3937; 38.3937; 38.3937
90; 90; 90		56595.2Cui, Hao; Wang, Yingxia; Wang, Yanhu; Fan, Yan-Zhong; Zhang, Li; Su, Cheng-Yong
A stable and porous iridium(iii)-porphyrin metal‒organic framework: synthesis, structure and catalysis
CrystEngComm, 2016, 18, 2203
7224255 CIFC55 H48 I6 N10 O9 Zn2P 1 21/n 18.813; 23.763; 14.62
90; 91.91; 90		3060.1Fernandez-Palacio, Francisco; Saccone, Marco; Priimagi, Arri; Terraneo, Giancarlo; Pilati, Tullio; Metrangolo, Pierangelo; Resnati, Giuseppe
Coordination networks incorporating halogen-bond donor sites and azobenzene groups
CrystEngComm, 2016, 18, 2251
7224256 CIFC58 H52 I6 N12 O10 ZnC 1 2/c 124.0554; 11.3346; 22.9563
90; 98.893; 90		6184Fernandez-Palacio, Francisco; Saccone, Marco; Priimagi, Arri; Terraneo, Giancarlo; Pilati, Tullio; Metrangolo, Pierangelo; Resnati, Giuseppe
Coordination networks incorporating halogen-bond donor sites and azobenzene groups
CrystEngComm, 2016, 18, 2251
7224257 CIFC33.42 H35.65 N6.81 O5.81 ZnP 1 21/c 110.1389; 14.9139; 23.1236
90; 95.194; 90		3482.2Fernandez-Palacio, Francisco; Saccone, Marco; Priimagi, Arri; Terraneo, Giancarlo; Pilati, Tullio; Metrangolo, Pierangelo; Resnati, Giuseppe
Coordination networks incorporating halogen-bond donor sites and azobenzene groups
CrystEngComm, 2016, 18, 2251
7224258 CIFC32 H32 O23 Zn3P n a 2119.4674; 5.92693; 31.1266
90; 90; 90		3591.45Ohtani, Masataka; Takase, Kazutaka; Wang, Pengyu; Higashi, Kouki; Ueno, Kimiyoshi; Yasuda, Nobuhiro; Sugimoto, Kunihisa; Furuta, Mamoru; Kobiro, Kazuya
Water-triggered macroscopic structural transformation of a metal‒organic framework
CrystEngComm, 2016, 18, 1866
7224263 CIFC14 H30 B16 Co2 N2 O10C 1 2/c 114.3465; 22.44; 19.3715
90; 92.822; 90		6228.8Boldog, Ishtvan; Bereciartua, Pablo J.; Bulánek, Roman; Kučeráková, Monika; Tomandlová, Markéta; Dušek, Michal; Macháček, Jan; De Vos, Dirk; Baše, Tomáš
10-Vertex closo-carborane: a unique ligand platform for porous coordination polymers
CrystEngComm, 2016, 18, 2036
7224264 CIFC11 H16 B16 Cu2 O11.4I 41 m d31.1622; 31.1622; 11.1615
90; 90; 90		10838.7Boldog, Ishtvan; Bereciartua, Pablo J.; Bulánek, Roman; Kučeráková, Monika; Tomandlová, Markéta; Dušek, Michal; Macháček, Jan; De Vos, Dirk; Baše, Tomáš
10-Vertex closo-carborane: a unique ligand platform for porous coordination polymers
CrystEngComm, 2016, 18, 2036
7224265 CIFC27.512 H58.127 B24 N3.102 O16.102 Zn4P n a 2120.8189; 23.3745; 12.7036
90; 90; 90		6182Boldog, Ishtvan; Bereciartua, Pablo J.; Bulánek, Roman; Kučeráková, Monika; Tomandlová, Markéta; Dušek, Michal; Macháček, Jan; De Vos, Dirk; Baše, Tomáš
10-Vertex closo-carborane: a unique ligand platform for porous coordination polymers
CrystEngComm, 2016, 18, 2036
7224279 CIFC26 H18 Co N4 O5P n n a21.638; 20.983; 12.364
90; 90; 90		5614Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224280 CIFC29 H25 Co N5 O6P 1 21/c 114.556; 12.648; 17.312
90; 110.84; 90		2978.7Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224281 CIFC26 H18 N4 O5 ZnC 1 2/c 110.284; 19.302; 11.701
90; 102.472; 90		2267.9Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224282 CIFC29 H25 Cd N5 O6P 1 21/c 114.298; 12.999; 16.979
90; 108.28; 90		2996.5Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224283 CIFC31 H29 Cd N5 O6P 1 21/c 114.261; 13.024; 17.038
90; 108.197; 90		3006.3Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224284 CIFC30 H27 Cd N5 O6P 1 21/c 114.499; 12.841; 16.771
90; 108.244; 90		2965.5Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224285 CIFC29 H25 Cu N5 O6P 1 21/c 114.268; 12.993; 16.902
90; 107.945; 90		2980.9Pal, Arun; Chand, Santanu; Senthilkumar, S.; Neogi, Subhadip; Das, Madhab C.
Structural variation of transition metal coordination polymers based on bent carboxylate and flexible spacer ligand: polymorphism, gas adsorption and SC-SC transmetallation
CrystEngComm, 2016, 18, 4323
7224286 CIFC18 H19 N O4P 1 21/c 112.713; 8.649; 15.231
90; 103.798; 90		1626Ramos, Rafael Rodrigues; da Silva, Cameron Capeletti; Guimarães, Freddy Fernandes; Martins, Felipe Terra
Polymorphism and conformerism in chalcones
CrystEngComm, 2016, 18, 2144
7224287 CIFC15 H11 N O4P -111.62; 13.232; 13.981
105.776; 90.626; 112.721		1891.8Ramos, Rafael Rodrigues; da Silva, Cameron Capeletti; Guimarães, Freddy Fernandes; Martins, Felipe Terra
Polymorphism and conformerism in chalcones
CrystEngComm, 2016, 18, 2144
7224288 CIFC30 H22 Cl8P 1 21/c 18.7874; 12.0308; 13.8215
90; 104.964; 90		1411.65Fabbiani, Francesca P. A.; Bergantin, Stefano; Gavezzotti, Angelo; Rizzato, Silvia; Moret, Massimo
X-ray diffraction and computational studies of the pressure-dependent tetrachloroethane solvation of diphenylanthracene
CrystEngComm, 2016, 18, 2173
7224289 CIFC26 H18C 1 2/c 110.4702; 13.3923; 12.0158
90; 89.931; 90		1684.9Fabbiani, Francesca P. A.; Bergantin, Stefano; Gavezzotti, Angelo; Rizzato, Silvia; Moret, Massimo
X-ray diffraction and computational studies of the pressure-dependent tetrachloroethane solvation of diphenylanthracene
CrystEngComm, 2016, 18, 2173
7224290 CIFC26 H18C 1 2/c 110.041; 13.15; 11.378
90; 88.483; 90		1501.8Fabbiani, Francesca P. A.; Bergantin, Stefano; Gavezzotti, Angelo; Rizzato, Silvia; Moret, Massimo
X-ray diffraction and computational studies of the pressure-dependent tetrachloroethane solvation of diphenylanthracene
CrystEngComm, 2016, 18, 2173
7224291 CIFC30 H22P 1 2/c 122.1305; 5.90728; 33.8663
90; 106.709; 90		4240.45Li, Ye-Xin; Yang, Xiao-Feng; Miao, Jin-Ling; Zhang, Zhen-Wei; Sun, Guo-Xin
Effects of substitution position on crystal packing, polymorphism and crystallization-induced emission of (9-anthryl)vinylstyrylbenzene isomers
CrystEngComm, 2016, 18, 2098
7224292 CIFC30 H22P c c n32.3617; 18.5058; 7.04172
90; 90; 90		4217.14Li, Ye-Xin; Yang, Xiao-Feng; Miao, Jin-Ling; Zhang, Zhen-Wei; Sun, Guo-Xin
Effects of substitution position on crystal packing, polymorphism and crystallization-induced emission of (9-anthryl)vinylstyrylbenzene isomers
CrystEngComm, 2016, 18, 2098

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 5 | Next 1000 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.