# Search results of SQL query from the Crystallography Open Database # Date and time performed: 2024-11-24T12:57:21+01:00 # Query: # SELECT data.* # FROM # data JOIN jaltnames # ON altname = journal # WHERE # (status is null or status != 'retracted') and # (journal_id IN (SELECT DISTINCT(journal_id) FROM jaltnames WHERE altname LIKE 'RSC advances') AND volume = 14 AND duplicateof IS NULL AND (status is NULL OR status != 'errors') AND (method is NULL OR method != 'theoretical')) # ORDER BY file asc file,a,siga,b,sigb,c,sigc,alpha,sigalpha,beta,sigbeta,gamma,siggamma,vol,sigvol,celltemp,sigcelltemp,diffrtemp,sigdiffrtemp,cellpressure,sigcellpressure,diffrpressure,sigdiffrpressure,thermalhist,pressurehist,compoundsource,nel,sg,sgHall,sgNumber,commonname,chemname,mineral,formula,calcformula,cellformula,Z,Zprime,acce_code,authors,title,journal,year,volume,issue,firstpage,lastpage,doi,method,radiation,wavelength,radType,radSymbol,Rall,Robs,Rref,wRall,wRobs,wRref,RFsqd,RI,gofall,gofobs,gofgt,gofref,duplicateof,optimal,status,flags,svnrevision,date,time,onhold "7247934","12.328","0.002","8.7496","0.0015","15.981","0.003","90","","102.026","0.003","90","","1686","0.5","296.15","","296.15","","","","","","","","","3","P 1 21 1","P 2yb","4","","R- (3,3'-phenyl)-5,5'6,6',7',8,8'-octahydro-[1,1'-dinaphthalene]-2,2'-diol","","- C39.2 H51.6 O5.6 -","- C32 H30 O2 -","- C64 H60 O4 -","2","1","","Li, Fangxiu; Sun, Yue; Sun, Xiaoxia; Hu, Yu","Self-assembled bamboo-like carbon nanotubes based on chiral H8BINOL sensors to recognize cinchonidine efficiently by diastereoisomer complexes","RSC Advances","2024","14","2","1134","1140","10.1039/D3RA08143E","","","0.71073","MoKα","","0.1243","0.0859","","","0.2423","0.2788","","","","","","1.015","","","","has coordinates,has disorder","288623","2024-01-03","02:33:43","" "7247935","7.5547","0.0008","10.3453","0.0011","11.0141","0.0012","87.479","0.003","80.687","0.002","70.175","0.001","799.07","0.15","298","2","298.15","","","","","","","","","6","P -1","-P 1","2","","","","- C16 H16 Cl N O2 S -","- C16 H16 Cl N O2 S -","- C32 H32 Cl2 N2 O4 S2 -","2","1","","Huang, Yu-Wen; Li, Jia-Zhuo; Yang, Feng; Zhang, Xi-Yu; Wang, Yan-Jing; Meng, Xin-Chao; Leng, Bo-Rong; Wang, De-Cai; Zhu, Yi-Long","Photocatalytic selective synthesis of (E)-β-aminovinyl sulfones and (E)-β-amidovinyl sulfones using Ru(bpy)3Cl2 as the catalyst","RSC Advances","2024","14","1","700","706","10.1039/D3RA08272E","","","0.71073","MoKα","","0.065","0.0489","","","0.1372","0.148","","","","","","1.088","","","","has coordinates","288624","2024-01-03","02:34:10","" "7247936","11.3419","0.0006","12.6437","0.0007","15.4793","0.0009","89.5519","0.0019","87.0296","0.0019","76.7371","0.0018","2157.7","0.2","","","","","","","","","","","","5","P -1","-P 1","2","","","","- C100 H76 F12 N8 O8 -","- C100 H76 F12 N8 O8 -","- C100 H76 F12 N8 O8 -","1","0.5","","Zhou, Feng-Ji; Zhu, Bao-Lei; Huang, Zhen-Hui; Lin, Ning; Zhang, Zhen-Wei","DBU-catalyzed diastereoselective 1,3-dipolar [3+2] cycloaddition of trifluoroethyl amine-derived isatin ketimines with chalcones: synthesis of 5′-CF3-substituted 3,2′-pyrrolidinyl spirooxindoles","RSC Advances","2024","14","1","548","551","10.1039/D3RA08127C","","","0.71076","MoKα","","0.1225","0.0635","","","0.1481","0.181","","","","","","1.0546","","","","has coordinates","288625","2024-01-03","02:34:44","" "7247937","6.011","0.003","15.789","0.008","21.392","0.011","73.242","0.006","83.793","0.007","86.176","0.006","1931.3","1.7","293","2","293.15","","","","","","","","","5","P -1","-P 1","2","","","","- C50 H36 N2 O5 Zn -","- C50 H36 N2 O5 Zn -","- C100 H72 N4 O10 Zn2 -","2","1","","Hossain, Ersad; Hazra, Abhijit; Datta, Sourav; Khan, Samim; Pramanik, Samit; Banerjee, Priyabrata; Mir, Mohammad Hedayetullah; Mukhopadhyay, Subrata","Facile construction of an anthracene-decorated highly luminescent coordination polymer for the selective detection of explosive nitroaromatics and the mutagenic pollutant TNP","RSC Advances","2024","14","1","397","404","10.1039/D3RA06926E","","","0.71073","MoKα","","0.0555","0.0409","","","0.0903","0.0967","","","","","","1.032","","","","has coordinates,has disorder","288626","2024-01-03","02:35:07","" "7247938","24.5506","0.0014","14.4941","0.0004","24.966","0.0013","90","","125.773","0.008","90","","7207.8","0.9","296","2","296.15","","","","","","","","","5","C 1 2 1","C 2y","5","","","","- C28.66667 H21 Cl N2 O3.33333 -","- C28.6667 H21 Cl N2 O3.33333 -","- C344 H252 Cl12 N24 O40 -","12","3","","Zhong, Jialing; Pan, Rihuang; Lin, Xufeng","Enantioselective synthesis of α-tetrasubstituted (1-indolizinyl) (diaryl)-methanamines via chiral phosphoric acid catalysis","RSC Advances","2024","14","2","1106","1113","10.1039/D3RA07636A","","","0.71073","MoKα","","0.0951","0.0516","","","0.1104","0.1289","","","","","","1.008","","","","has coordinates","295862","2024-11-09","12:08:13","" "7247939","7.2177","0.0003","9.2009","0.0004","27.0007","0.0017","90","","90","","90","","1793.1","0.16","293","","293","","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","Mebendazolium mesylate anhydride salt","","- C17 H17 N3 O6 S -","- C17 H17 N3 O6 S -","- C68 H68 N12 O24 S4 -","4","1","","Gutiérrez, Eduardo L.; Godoy, Agustín A.; Brusau, Elena V.; Vega, Daniel; Narda, Griselda E.; Suárez, Sebastián; Di Salvo, Florencia","Mebendazolium mesylate anhydride salt: rational design based on supramolecular assembly, synthesis, and solid-state characterization","RSC Advances","2024","14","1","181","192","10.1039/D3RA07422F","","x-ray","1.54184","CuKα","","0.0773","0.0628","","","0.1717","0.1814","","","","","","1.123","","","","has coordinates","288628","2024-01-03","02:36:08","" "7247940","15.6599","0.0013","16.5029","0.0014","17.2608","0.0014","90","","90","","90","","4460.8","0.6","240","2","240","2","","","","","","","synthesis","5","P 21 21 21","P 2ac 2ab","19","Phe(Me)ASC","cyclo(Phe(Me)-Oxz-D-Val-Thz-Ile-Oxz-D-Val-Thz).MeCN","","- C42 H55 N9 O6 S2 -","- C42 H55 N9 O6 S2 -","- C168 H220 N36 O24 S8 -","4","1","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","0.71073","MoKα","","0.0717","0.0681","","","0.1719","0.1749","","","","","","1.096","","","","has coordinates","288629","2024-01-03","02:37:30","" "7247941","13.7742","0.0006","21.713","0.0016","15.1389","0.0006","90","","91.337","0.004","90","","4526.5","0.4","100","","100","","","","","","","","synthesis","6","P 1 21 1","P 2yb","4","","Phe(4I)_ASC","","- C41 H53.5 I N8.5 O6.5 S2 -","- C41 H53 I N8.5 O6.5 S2 -","- C164 H212 I4 N34 O26 S8 -","4","2","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","1.54184","CuKα","","0.1296","0.1093","","","0.293","0.3125","","","","","","1.17","","","","has coordinates","295677","2024-10-30","18:34:33","" "7247942","9.4424","0.0004","9.8919","0.0004","12.937","0.0006","80.097","0.004","80.867","0.004","84.776","0.004","1172.74","0.09","100","","100","","","","","","","","synthesis","6","P 1","P 1","1","","Phe(4cf3)_ASC","","- C43 H53 F3 N8 O7 S2 -","- C43 H53 F3 N8 O7 S2 -","- C43 H53 F3 N8 O7 S2 -","1","1","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","1.54184","CuKα","","0.1541","0.1268","","","0.355","0.3792","","","","","","1.5","","","","has coordinates","288629","2024-01-03","02:37:31","" "7247943","9.3885","0.0001","10.0778","0.0002","13.0183","0.0002","82.659","0.001","86.078","0.001","80.131","0.001","1202.19","0.03","100","","100","","","","","","","","synthesis","5","P 1","P 1","1","","Phe(tbu)_ASC","","- C45 H63 N9 O7 S2 -","- C45 H63 N9 O7 S2 -","- C45 H63 N9 O7 S2 -","1","1","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","1.54184","CuKα","","0.0478","0.0462","","","0.1315","0.1343","","","","","","1.047","","","","has coordinates","288629","2024-01-03","02:37:31","" "7247944","15.648","0.0001","16.8169","0.0002","16.1537","0.0002","90","","95.683","0.001","90","","4229.97","0.08","100","","100","","","","","","","","synthesis","6","P 1 21 1","P 2yb","4","","Phe(4Br)_ASC","","- C40 H50.5 Br N8.5 O6 S2 -","- C40 H50.5 Br N8.5 O6 S2 -","- C160 H202 Br4 N34 O24 S8 -","4","2","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","1.54184","CuKα","","0.0828","0.0719","","","0.1901","0.2378","","","","","","1.069","","","","has coordinates","295677","2024-10-30","18:34:33","" "7247945","15.6272","0.0002","16.6962","0.0002","16.1368","0.0002","90","","95.44","0.001","90","","4191.37","0.09","90","","90","","","","","","","","","6","P 1 21 1","P 2yb","4","","Phe(4Cl)_ASC","","- C40 H50.5 Cl N8.5 O6 S2 -","- C40 H50.5 Cl N8.5 O6 S2 -","- C160 H202 Cl4 N34 O24 S8 -","4","2","","Asano, Akiko; Kawanami, Yukiko; Fujita, Mao; Yano, Yuta; Ide, Rio; Minoura, Katsuhiko; Kato, Takuma; Doi, Mitsunobu","Electronic substituent effect on the conformation of a phenylalanine-incorporated cyclic peptide","RSC Advances","2024","14","2","1062","1071","10.1039/D3RA07836A","","","1.54184","CuKα","","0.0436","0.0428","","","0.1329","0.1337","","","","","","0.718","","","","has coordinates","288629","2024-01-03","02:37:31","" "7247946","10.2257","0.0009","14.332","0.0016","14.3731","0.0014","106.76","0.004","110.599","0.004","105.352","0.004","1723.2","0.3","150","","150","","","","","","","","","7","P 1","P 1","1","","","","- C20 H52.78 Cr2 Cu4 Mo12 N12 O61.39 -","- C20 H50.8 Cr2 Cu4 Mo12 N12 O61.4 -","- C20 H50.8 Cr2 Cu4 Mo12 N12 O61.4 -","1","1","","Tan, Hong-Ru; Zhou, Xiang; Gong, Tengfei; You, Hanqi; Zheng, Qi; Zhao, Sheng-Yin; Xuan, Weimin","Anderson-type polyoxometalate-based metal–organic framework as an efficient heterogeneous catalyst for selective oxidation of benzylic C–H bonds","RSC Advances","2024","14","1","364","372","10.1039/D3RA07120K","","x-ray","0.71073","MoKα","","0.0587","0.0506","","","0.1169","0.1251","","","","","","1.026","","","","has coordinates,has disorder","288630","2024-01-03","02:38:15","" "7247951","12.387","0.003","6.2596","0.0017","33.747","0.009","90","","91.613","0.003","90","","2615.6","1.2","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H26 Fe O4 Se2 -","- C28 H26 Fe O4 Se2 -","- C112 H104 Fe4 O16 Se8 -","4","1","","Yang, Zhuo; Wang, Jinshan; Li, Aimin; Wang, Chao; Ji, Wei; Pires, Elísabet; Yang, Wenzhong; Jing, Su","Ferrocenylselenoether and its cuprous cluster modified TiO2 as visible-light photocatalyst for the synergistic transformation of N-cyclic organics and Cr(vi)","RSC Advances","2024","14","2","1488","1500","10.1039/D3RA07390D","","","0.71073","MoKα","","0.1038","0.0785","","","0.1908","0.1999","","","","","","1.101","","","","has coordinates","288672","2024-01-04","02:24:50","" "7248030","12.95","0.0006","20.3971","0.0011","15.0471","0.0007","90","","100.379","0.001","90","","3909.5","0.3","273.15","","273.15","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C54.02 H76.29 Cd2 Cl8 N27.98 O22 -","- C54.04 H76.294 Cd2 Cl8 N27.974 O22 -","- C108.08 H152.588 Cd4 Cl16 N55.948 O44 -","2","0.5","","Ye, Yanan; Ma, Peihua; Ma, Yue; Yang, Naqin; Chen, Xiaoqian; Yang, Xinan; Shen, Lingyi; Xiao, Xin","Study on the host–guest interactions between tetramethyl cucurbit[6]uril and 2-heterocyclic-substituted benzimidazoles","RSC Advances","2024","14","4","2652","2658","10.1039/D3RA07810H","","","0.71073","MoKα","","0.0924","0.0798","","","0.2304","0.2403","","","","","","1.115","","","","has coordinates,has disorder","289115","2024-01-17","02:32:43","" "7248031","23.088","0.006","11.877","0.003","15.998","0.007","90","","131.526","0.006","90","","3284.3","1.9","290","","290","","","","","","","","","4","C 1 2 1","C 2y","5","","","","- C52 H54 N27 O12 -","- C52 H50 N27 O12 -","- C104 H100 N54 O24 -","2","0.5","","Ye, Yanan; Ma, Peihua; Ma, Yue; Yang, Naqin; Chen, Xiaoqian; Yang, Xinan; Shen, Lingyi; Xiao, Xin","Study on the host–guest interactions between tetramethyl cucurbit[6]uril and 2-heterocyclic-substituted benzimidazoles","RSC Advances","2024","14","4","2652","2658","10.1039/D3RA07810H","","","0.71073","MoKα","","0.1868","0.1215","","","0.3162","0.3638","","","","","","1.222","","","","has coordinates","289115","2024-01-17","02:32:46","" "7248032","13.5914","0.001","17.2592","0.0012","33.599","0.002","82.721","0.002","79.158","0.002","72.244","0.002","7351.8","0.9","273.15","","273.15","","","","","","","","","6","P -1","-P 1","2","","","","- C106 H108 Cl12 N52 O24 Zn3 -","- C106 H108 Cl12 N52 O24 Zn3 -","- C212 H216 Cl24 N104 O48 Zn6 -","2","1","","Ye, Yanan; Ma, Peihua; Ma, Yue; Yang, Naqin; Chen, Xiaoqian; Yang, Xinan; Shen, Lingyi; Xiao, Xin","Study on the host–guest interactions between tetramethyl cucurbit[6]uril and 2-heterocyclic-substituted benzimidazoles","RSC Advances","2024","14","4","2652","2658","10.1039/D3RA07810H","","","0.71073","MoKα","","0.1579","0.1082","","","0.3069","0.3315","","","","","","1.043","","","","has coordinates,has disorder","289115","2024-01-17","02:32:47","" "7248037","15.7011","0.0014","15.7011","0.0014","29.337","0.003","90","","90","","90","","7232.3","1.2","103","2","103","","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C44 H36 N6 O5 -","- C44 H36 N6 O5 -","- C352 H288 N48 O40 -","8","0.5","","Patil, Baliram R.; Nichinde, Chandrakant B.; Chaudhari, Suryakant S.; Krishna, Gamidi Rama; Kinage, Anil K.","Organocatalyzed [4 + 2] cycloaddition of α,β-unsaturated ketones and isatylidene malononitrile: accessing spiro[3-arylcyclohexanone]oxindole derivatives","RSC Advances","2024","14","5","2873","2877","10.1039/D3RA07652K","","","0.71073","MoKα","","0.0459","0.0374","","","0.0906","0.0967","","","","","","1.016","","","","has coordinates","289135","2024-01-18","02:48:46","" "7248038","9.9591","0.0004","17.0919","0.0006","11.8583","0.0005","90","","105.357","0.001","90","","1946.45","0.13","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C24 H21 N3 O2 -","- C24 H21 N3 O2 -","- C96 H84 N12 O8 -","4","1","","Patil, Baliram R.; Nichinde, Chandrakant B.; Chaudhari, Suryakant S.; Krishna, Gamidi Rama; Kinage, Anil K.","Organocatalyzed [4 + 2] cycloaddition of α,β-unsaturated ketones and isatylidene malononitrile: accessing spiro[3-arylcyclohexanone]oxindole derivatives","RSC Advances","2024","14","5","2873","2877","10.1039/D3RA07652K","","","0.71073","MoKα","","0.057","0.0513","","","0.1228","0.1271","","","","","","1.027","","","","has coordinates","289135","2024-01-18","02:48:50","" "7248090","11.19","0.0005","13.4371","0.0005","7.0568","0.0003","90","","98.472","0.003","90","","1049.49","0.08","299.82","0.1","299.82","0.1","","","","","","","","3","C 1 2/m 1","-C 2y","12","","MTQ","","- C27 H16 N4 -","- C27 H15.5 N4 -","- C54 H31 N8 -","2","0.25","","Wen, Xinyi; Shao, Yixin; Chen, Ye-Tao; He, Jiaxing; Chen, Shun-Li; Dang, Li; Li, Ming-De","Dual-rotor strategy for organic cocrystals with enhanced near-infrared photothermal conversion","RSC Advances","2024","14","7","4503","4508","10.1039/D4RA00002A","","x-ray","1.54184","CuKα","","0.0691","0.0609","","","0.1871","0.197","","","","","","1.093","","","","has coordinates,has disorder","289299","2024-02-03","02:24:46","" "7248091","6.7935","0.0003","8.9755","0.0004","17.3317","0.0007","102.064","0.004","90.087","0.003","96.951","0.004","1025.47","0.08","100","0.1","100","0.1","","","","","","","","3","P -1","-P 1","2","","DTQ","","- C28 H18 N4 -","- C28 H18 N4 -","- C56 H36 N8 -","2","1","","Wen, Xinyi; Shao, Yixin; Chen, Ye-Tao; He, Jiaxing; Chen, Shun-Li; Dang, Li; Li, Ming-De","Dual-rotor strategy for organic cocrystals with enhanced near-infrared photothermal conversion","RSC Advances","2024","14","7","4503","4508","10.1039/D4RA00002A","","x-ray","1.54184","CuKα","","0.0407","0.0389","","","0.1103","0.1122","","","","","","1.04","","","","has coordinates","289299","2024-02-03","02:24:47","" "7248092","7.7988","0.0002","8.4619","0.0002","16.7251","0.0004","82.874","0.002","80.374","0.002","83.233","0.002","1074.46","0.05","99.98","0.1","99.98","0.1","","","","","","","","4","P -1","-P 1","2","","DFQ","","- C28 H14 F4 N4 -","- C28 H14 F4 N4 -","- C56 H28 F8 N8 -","2","1","","Wen, Xinyi; Shao, Yixin; Chen, Ye-Tao; He, Jiaxing; Chen, Shun-Li; Dang, Li; Li, Ming-De","Dual-rotor strategy for organic cocrystals with enhanced near-infrared photothermal conversion","RSC Advances","2024","14","7","4503","4508","10.1039/D4RA00002A","","x-ray","1.54184","CuKα","","0.0386","0.0371","","","0.0991","0.1007","","","","","","1.068","","","","has coordinates","289299","2024-02-03","02:24:47","" "7248093","12.729","0.009","15.65","0.003","19.849","0.005","91.255","0.005","91.14","0.03","103.68","0.03","3840","3","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C146.4 H175.2 N16 O25.2 S9.2 -","- C146.4 H175.2 N16 O25.2 S9.2 -","- C146.4 H175.2 N16 O25.2 S9.2 -","1","0.5","","Milone, Marco; Pisagatti, Ilenia; Gattuso, Giuseppe; Notti, Anna; Parisi, Melchiorre F.; Brancatelli, Giovanna; Hickey, Neal; Geremia, Silvano","Influence of H-bond competitors on the solvent-dependent structures of an octaurea-calix[4]tube","RSC Advances","2024","14","7","4448","4455","10.1039/D3RA08764F","","","0.7","synchrotron","","0.1571","0.1229","","","0.3308","0.3694","","","","","","1.007","","","","has coordinates,has disorder","289300","2024-02-03","02:25:23","" "7248094","40.093","0.014","22.414","0.005","18.799","0.003","90","","107.521","0.012","90","","16110","7","100","2","100","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C143.2 H169.6 N16 O25.6 S7.6 -","- C135.2 H145.6 N16 O21.6 S3.6 -","- C540.8 H582.4 N64 O86.4 S14.4 -","4","0.5","","Milone, Marco; Pisagatti, Ilenia; Gattuso, Giuseppe; Notti, Anna; Parisi, Melchiorre F.; Brancatelli, Giovanna; Hickey, Neal; Geremia, Silvano","Influence of H-bond competitors on the solvent-dependent structures of an octaurea-calix[4]tube","RSC Advances","2024","14","7","4448","4455","10.1039/D3RA08764F","","","1","synchrotron","","0.1539","0.141","","","0.3647","0.381","","","","","","1.104","","","","has coordinates,has disorder","289300","2024-02-03","02:25:24","" "7248095","9.2475","0.0173","9.9092","0.0187","11.8955","0.0222","70.528","0.022","67.961","0.021","73.477","0.023","937","3","300","2","300","2","","","","","","","","7","P -1","-P 1","2","","3-(4-chlorophenyl)-2-((4-fluorophenyl)selanyl)benzo[4,5] imidazo[2,1-b]thiazole","","- C21 H12 Cl F N2 S Se -","- C21 H12 Cl F N2 S Se -","- C42 H24 Cl2 F2 N4 S2 Se2 -","2","1","","Ghosh, Prasanjit; Chhetri, Gautam; Mandal, Anirban; Chen, Yu; Hersh, William H.; Das, Sajal","C(sp2)–H selenylation of substituted benzo[4,5]imidazo[2,1-b]thiazoles using phenyliodine(iii)bis(trifluoroacetate) as a mediator","RSC Advances","2024","14","7","4462","4470","10.1039/D4RA00057A","","","0.71073","MoKα","","0.0637","0.0332","","","0.0713","0.0782","","","","","","0.925","","","","has coordinates","289301","2024-02-03","02:25:39","" "7248098","7.9767","0.0007","9.0843","0.0008","9.3456","0.0008","86.352","0.006","69.069","0.005","74.829","0.005","610.14","0.1","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C12 H18 Cl8 N4 Sb2 -","- C12 H18 Cl8 N4 Sb2 -","- C12 H18 Cl8 N4 Sb2 -","1","0.5","","Chaabane, I.; Rekik, W.; Ghalla, H.; Zaghrioui, M.; Lhoste, J.; Oueslati, A.","Crystal structure, optical characterization, conduction and relaxation mechanisms of a new hybrid compound (C6H9N2)2[Sb2Cl8].","RSC advances","2024","14","5","3588","3598","10.1039/d3ra08885e","","","0.71073","MoKα","","0.0341","0.0256","","","0.0424","0.0451","","","","","","1.038","","","","has coordinates","289309","2024-02-04","10:00:41","" "7248101","9.4933","0.0003","9.0418","0.0003","21.8135","0.0009","90","","101.356","0.004","90","","1835.74","0.12","170","0.1","170","0.1","","","","","","","","4","I 1 2/a 1","-I 2ya","15","","","","- C10 H10 N2 O -","- C10 H10 N2 O -","- C80 H80 N16 O8 -","8","1","","Chen, Yichun; Lu, Ziqi; He, Wenfen; Zhu, Huanyi; Lu, Weilong; Shi, Junjun; Sheng, Jie; Xie, Wucheng","Rhodium-catalyzed annulation of hydrazines with vinylene carbonate to synthesize unsubstituted 1-aminoindole derivatives","RSC Advances","2024","14","7","4804","4809","10.1039/D3RA07466H","","x-ray","1.54184","CuKα","","0.0542","0.049","","","0.1323","0.1388","","","","","","1.035","","","","has coordinates","289733","2024-02-07","02:24:29","" "7248110","9.3292","0.0016","14.298","0.002","14.191","0.003","90","","96.46","0.006","90","","1880.9","0.6","300","","300","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C23 H17 N3 S -","- C23 H17 N3 S -","- C92 H68 N12 S4 -","4","1","","Vinayagam, Dhandapani; Subramanian, Karpagam","A phenothiazine-functionalized pyridine-based AIEE-active molecule: a versatile molecular probe for highly sensitive detection of hypochlorite and picric acid","RSC Advances","2024","14","8","5149","5158","10.1039/D3RA08451E","","x-ray","0.71073","MoKα","","0.1149","0.0547","","","0.1015","0.1283","","","","","","1.055","","","","has coordinates","289765","2024-02-09","02:31:59","" "7248118","13.5911","0.0003","14.1632","0.0004","23.9764","0.0006","94.222","0.002","93.435","0.002","106.38","0.002","4400.2","0.2","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C108.85 H90.7 Cl0.7 O3.75 -","- C108.85 H90.7 Cl0.7 O3.75 -","- C217.7 H181.4 Cl1.4 O7.5 -","2","1","","Younes, Eyad A.; Hammad, Yamen J.; Salami, Fatemeh; Rasras, Anas J.; Al-Qawasmeh, Raed A.; Zhao, Yuming","Electron-donating arene-substituted pentacenedione derivatives: a study of structural, electronic, and electrochemical properties","RSC Advances","2024","14","8","5331","5339","10.1039/D3RA05173K","","x-ray","1.54184","CuKα","","0.1345","0.1026","","","0.3072","0.3434","","","","","","1.269","","","","has coordinates,has disorder","289779","2024-02-10","02:24:15","" "7248119","7.3252","0.0001","22.6642","0.0002","23.2798","0.0002","90","","92.451","0.001","90","","3861.37","0.07","100","2","100","2","","","","","","","","3","I 1 a 1","I -2ya","9","","","","- C52 H38 O6 -","- C52 H38 O6 -","- C208 H152 O24 -","4","1","","Younes, Eyad A.; Hammad, Yamen J.; Salami, Fatemeh; Rasras, Anas J.; Al-Qawasmeh, Raed A.; Zhao, Yuming","Electron-donating arene-substituted pentacenedione derivatives: a study of structural, electronic, and electrochemical properties","RSC Advances","2024","14","8","5331","5339","10.1039/D3RA05173K","","x-ray","1.54184","CuKα","","0.0449","0.0434","","","0.1115","0.1127","","","","","","1.056","","","","has coordinates","289779","2024-02-10","02:24:16","" "7248120","15.9867","0.0009","5.3642","0.0003","21.1924","0.0011","90","","103.788","0.002","90","","1765","0.17","298","","298","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C17 H28 N2 O2 -","- C17 H27 N2 O2 -","- C68 H108 N8 O8 -","4","1","","Camargo-Ayala, Lorena; Bedoya, Mauricio; Prent-Peñaloza, Luis; Polo-Cuadrado, Efraín; Osorio, Edison; Brito, Iván; Delgado, Gerzon E.; González, Wendy; Gutierrez, Margarita","Crystal structure, quantum chemical insights, and molecular docking studies of Naryl-2-(N-disubstituted) acetamide compounds: potential inhibitors for neurodegenerative enzymes","RSC Advances","2024","14","8","5222","5233","10.1039/D3RA08649F","","","0.71073","MoKα","","0.172","0.0843","","","0.2074","0.2756","","","","","","1.081","","","","has coordinates,has disorder","289780","2024-02-10","02:24:56","" "7248121","4.763","0.007","10.544","0.016","15.14","0.02","90","","96.49","0.04","90","","755.5","1.9","298","","298","","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C17 H17 N2 O -","- C17 H20 N2 O -","- C34 H40 N4 O2 -","2","1","","Camargo-Ayala, Lorena; Bedoya, Mauricio; Prent-Peñaloza, Luis; Polo-Cuadrado, Efraín; Osorio, Edison; Brito, Iván; Delgado, Gerzon E.; González, Wendy; Gutierrez, Margarita","Crystal structure, quantum chemical insights, and molecular docking studies of Naryl-2-(N-disubstituted) acetamide compounds: potential inhibitors for neurodegenerative enzymes","RSC Advances","2024","14","8","5222","5233","10.1039/D3RA08649F","","","0.71073","MoKα","","0.3128","0.0847","","","0.1055","0.1474","","","","","","0.87","","","","has coordinates","289780","2024-02-10","02:24:57","" "7248122","14.1335","0.0011","10.5456","0.0007","22.1248","0.0017","90","","90","","90","","3297.6","0.4","298","","298","","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C16 H26 N2 O -","- C16 H26 N2 O -","- C128 H208 N16 O8 -","8","1","","Camargo-Ayala, Lorena; Bedoya, Mauricio; Prent-Peñaloza, Luis; Polo-Cuadrado, Efraín; Osorio, Edison; Brito, Iván; Delgado, Gerzon E.; González, Wendy; Gutierrez, Margarita","Crystal structure, quantum chemical insights, and molecular docking studies of Naryl-2-(N-disubstituted) acetamide compounds: potential inhibitors for neurodegenerative enzymes","RSC Advances","2024","14","8","5222","5233","10.1039/D3RA08649F","","","0.71073","MoKα","","0.1708","0.0673","","","0.1301","0.1565","","","","","","0.856","","","","has coordinates","289780","2024-02-10","02:24:58","" "7248123","7.1033","0.0004","23.7608","0.0014","18.3655","0.0011","90","","93.527","0.004","90","","3093.9","0.3","298.15","","298.15","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C15 H22 N2 O3 -","- C15 H22 N2 O3 -","- C120 H176 N16 O24 -","8","2","","Camargo-Ayala, Lorena; Bedoya, Mauricio; Prent-Peñaloza, Luis; Polo-Cuadrado, Efraín; Osorio, Edison; Brito, Iván; Delgado, Gerzon E.; González, Wendy; Gutierrez, Margarita","Crystal structure, quantum chemical insights, and molecular docking studies of Naryl-2-(N-disubstituted) acetamide compounds: potential inhibitors for neurodegenerative enzymes","RSC Advances","2024","14","8","5222","5233","10.1039/D3RA08649F","","","1.54178","CuKα","","0.1045","0.0643","","","0.1769","0.2058","","","","","","1.03","","","","has coordinates","292638","2024-06-28","09:33:37","" "7248127","7.788","0.0005","8.7699","0.0005","9.7291","0.0006","111.057","0.002","96.558","0.002","104.436","0.002","585.08","0.06","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C13 H13 Cl N2 O -","- C13 H13 Cl N2 O -","- C26 H26 Cl2 N4 O2 -","2","1","","Pawlędzio, Sylwia; Ziemniak, Marcin; Trzybiński, Damian; Arhangelskis, Mihails; Makal, Anna; Woźniak, Krzysztof","Influence of N-protonation on electronic properties of acridine derivatives by quantum crystallography","RSC Advances","2024","14","8","5340","5350","10.1039/D3RA08081A","","","0.71073","MoKα","","0.0186","0.0139","","","0.0387","0.0426","","","","","","1.178","","","","has coordinates","289799","2024-02-13","02:27:56","" "7248128","7.788","0.0005","8.7699","0.0005","9.7291","0.0006","111.057","0.002","96.558","0.002","104.436","0.002","585.08","0.06","100","2","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C13 H13 Cl N2 O -","- C13 H13 Cl N2 O -","- C26 H26 Cl2 N4 O2 -","2","1","","Pawlędzio, Sylwia; Ziemniak, Marcin; Trzybiński, Damian; Arhangelskis, Mihails; Makal, Anna; Woźniak, Krzysztof","Influence of N-protonation on electronic properties of acridine derivatives by quantum crystallography","RSC Advances","2024","14","8","5340","5350","10.1039/D3RA08081A","","","0.71073","MoKα","","0.0268","0.0213","","","0.0706","0.074","","","","","","1.029","","","","has coordinates","289799","2024-02-13","02:27:57","" "7248129","24.31","0.003","24.31","0.003","14.016","0.002","90","","90","","90","","8283.1","1.9","100","0.1","100","0.1","","","","","","","","4","I 41/a c d :2","-I 4bd 2c","142","","","","- C13 H11 N2 O0.5 -","- C13 H11 N2 O0.5 -","- C416 H352 N64 O16 -","32","1","","Pawlędzio, Sylwia; Ziemniak, Marcin; Trzybiński, Damian; Arhangelskis, Mihails; Makal, Anna; Woźniak, Krzysztof","Influence of N-protonation on electronic properties of acridine derivatives by quantum crystallography","RSC Advances","2024","14","8","5340","5350","10.1039/D3RA08081A","","","0.71073","MoKα","","0.0427","0.0305","","","0.0901","0.0941","","","","","","0.911","","","","has coordinates","289799","2024-02-13","02:27:57","" "7248130","24.31","0.002","24.31","0.002","14.016","0.002","90","","90","","90","","8283.1","1.5","100","0.1","100","0.1","","","","","","","","4","I 41/a c d :2","-I 4bd 2c","142","","","","- C26 H22 N4 O -","- C26 H22 N4 O -","- C416 H352 N64 O16 -","16","0.5","","Pawlędzio, Sylwia; Ziemniak, Marcin; Trzybiński, Damian; Arhangelskis, Mihails; Makal, Anna; Woźniak, Krzysztof","Influence of N-protonation on electronic properties of acridine derivatives by quantum crystallography","RSC Advances","2024","14","8","5340","5350","10.1039/D3RA08081A","","x-ray","1.54184","CuKα","","0.0548","0.0418","","","0.1226","0.128","","","","","","1.041","","","","has coordinates","289799","2024-02-13","02:27:57","" "7248179","8.0992","0.0004","20.6903","0.0011","9.9276","0.0006","90","","111.728","0.002","90","","1545.42","0.15","273","2","273","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C20 H15 N3 O -","- C20 H15 N3 O -","- C80 H60 N12 O4 -","4","1","","Zuo, Youpeng; Liu, Meijun; Du, Jun; Zhang, Tianren; Wang, Xiaoqing; Wang, Cong","Ir(iii)/Ag(i)-catalyzed directly C–H amidation of arenes with OH-free hydroxyamides as amidating agents","RSC Advances","2024","14","9","5975","5980","10.1039/D4RA00517A","","","0.71073","MoKα","","0.0565","0.0505","","","0.1169","0.1225","","","","","","1.078","","","","has coordinates","289842","2024-02-16","02:33:34","" "7248180","7.6763","0.001","7.938","0.001","8.2274","0.0011","73.068","0.004","67.252","0.004","68.824","0.004","424.37","0.1","300","2","300","2","","","","","","","","4","P -1","-P 1","2","","","","- C6 H7 O6 Rb -","- C6 H7 O6 Rb -","- C12 H14 O12 Rb2 -","2","1","","Kavitha, S.; Vizhi, R. Ezhil","Investigation on the growth aspects and properties of rubidium hydrogen succinate hydrate single crystal for NLO applications","RSC Advances","2024","14","9","6016","6027","10.1039/D3RA07579F","","","0.71073","MoKα","","0.0341","0.0292","","","0.0697","0.0725","","","","","","1.023","","","","has coordinates","289858","2024-02-17","02:30:08","" "7248182","5.41865","0.00009","5.41865","0.00009","26.3535","0.0005","90","","90","","120","","670.12","0.02","292.09","0.1","292.09","0.1","","","","","","","","5","P 63/m m c","-P 6c 2c","194","","","","- B4 Ba4 Bi O13 Tb -","- B4 Ba4 Bi O13 Tb -","- B8 Ba8 Bi2 O26 Tb2 -","2","0.0833333","","Chen, Xuean; Yuan, Xuyang; Xiao, Weiqiang; Song, Xiaoyan","Two new rare-earth oxyborates Ba4BiTbO(BO3)4 and Ba1.54Sr2.46BiTbO(BO3)4 and luminescence properties of the Ba4BiTb1−xEuxO(BO3)4 phosphors","RSC Advances","2024","14","9","6270","6284","10.1039/D3RA08265B","","x-ray","0.71073","MoKα","","0.0464","0.0417","","","0.0964","0.0988","","","","","","1.173","","","","has coordinates","289875","2024-02-20","02:25:17","" "7248183","5.36534","0.00019","5.36534","0.00019","26.0661","0.001","90","","90","","120","","649.83","0.04","292.09","0.1","292.09","0.1","","","","","","","","6","P 63/m m c","-P 6c 2c","194","","","","- B4 Ba1.54 Bi O13 Sr2.46 Tb -","- B4 Ba1.54 Bi O13 Sr2.46 Tb -","- B8 Ba3.08 Bi2 O26 Sr4.92 Tb2 -","2","0.0833333","","Chen, Xuean; Yuan, Xuyang; Xiao, Weiqiang; Song, Xiaoyan","Two new rare-earth oxyborates Ba4BiTbO(BO3)4 and Ba1.54Sr2.46BiTbO(BO3)4 and luminescence properties of the Ba4BiTb1−xEuxO(BO3)4 phosphors","RSC Advances","2024","14","9","6270","6284","10.1039/D3RA08265B","","x-ray","0.71073","MoKα","","0.0645","0.0604","","","0.1077","0.1094","","","","","","1.121","","","","has coordinates","289875","2024-02-20","02:25:18","" "7248184","7.4729","0.001","16.121","0.002","19.743","0.003","67.095","0.01","88.242","0.011","84.135","0.011","2179.3","0.5","193","2","193","2","","","","","","","","6","P -1","-P 1","2","","3,6-Bis(5-(4,4,5,5-tetramethyl-4,5-dihydro-3oxid-1-oxyl-1-H-imidazol-2-yl)-thiophene-2yl)-2,5-dihexyl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione","","- C41 H56 Cl2 N6 O6 S2 -","- C41 H56 Cl2 N6 O6 S2 -","- C82 H112 Cl4 N12 O12 S4 -","2","1","","Tretyakov, Evgeny; Gorbunov, Dmitry; Gritsan, Nina; Keerthi, Ashok; Baumgarten, Martin; Schollmeyer, Dieter; Ivanov, Mikhail; Sergeeva, Anna; Fedin, Matvey","Synthesis and photoinduced behavior of DPP-anchored nitronyl nitroxides: a multifaceted approach","RSC Advances","2024","14","9","6178","6189","10.1039/D4RA00916A","","","1.54178","CuKα","","0.343","0.1407","","","0.3299","0.4395","","","","","","0.883","","","","has coordinates,has disorder","289876","2024-02-20","02:25:34","" "7248185","22.042","0.005","3.9504","0.0009","15.024","0.003","90","","104.448","0.003","90","","1266.8","0.5","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C16 H14 O4 -","- C16 H14 O4 -","- C64 H56 O16 -","4","0.5","","Lee, Sae Hui; Valverde Paredes, Marco S.; Forster, Paul M.; Lee, Dong-Chan","Side group dependent room temperature crystallization-induced phosphorescence of benzil based all organic phosphors","RSC Advances","2024","14","9","6285","6291","10.1039/D4RA00816B","","","0.71073","MoKα","","0.0476","0.0434","","","0.1209","0.1262","","","","","","1.06","","","","has coordinates","289877","2024-02-20","02:25:52","" "7248186","22.098","0.008","4.7567","0.0017","26.394","0.01","90","","109.636","0.005","90","","2613","1.7","100","2","100","2","","","","","","","","3","C 1 2/c 1","-C 2yc","15","","","","- C30 H42 O4 -","- C30 H42 O4 -","- C120 H168 O16 -","4","0.5","","Lee, Sae Hui; Valverde Paredes, Marco S.; Forster, Paul M.; Lee, Dong-Chan","Side group dependent room temperature crystallization-induced phosphorescence of benzil based all organic phosphors","RSC Advances","2024","14","9","6285","6291","10.1039/D4RA00816B","","","0.71073","MoKα","","0.0631","0.0472","","","0.123","0.1332","","","","","","1.116","","","","has coordinates","289877","2024-02-20","02:25:52","" "7248208","7.8389","0.0008","13.8151","0.0016","17.198","0.002","90","","94.032","0.004","90","","1857.9","0.4","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","1-((Z)-((4-((E)-N-(thiazol-2(3H)-ylidene)sulfamoyl)phenyl)iminio)methylnaphthalen-2-olate","","- C20 H15 N3 O3 S2 -","- C20 H15 N3 O3 S2 -","- C80 H60 N12 O12 S8 -","4","1","","Malik, Abida Naseem; Ali, Akbar; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Alam, Mohammad Mahtab; Mostafa, Mohamed S.; Kuznetsov, Aleksey","A synthetic approach towards drug modification: 2-hydroxy-1-naphthaldehyde based imine-zwitterion preparation, single-crystal study, Hirshfeld surface analysis, and computational investigation","RSC Advances","2024","14","10","6476","6493","10.1039/D3RA08727A","","","0.71073","MoKα","","0.0852","0.0437","","","0.0916","0.1087","","","","","","1.018","","","","has coordinates","289926","2024-02-22","02:35:08","" "7248209","4.5436","0.0006","12.5255","0.0016","17.673","0.002","88.308","0.008","89.195","0.008","82.611","0.009","996.9","0.2","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","(E)-1-(((4-amino-5-(4-chlorophenyl)-6-ethylpyrimidin-2-yl)iminio)methyl) naphthalen-2-olate","","- C23 H19 Cl N4 O -","- C23 H19 Cl N4 O -","- C46 H38 Cl2 N8 O2 -","2","1","","Malik, Abida Naseem; Ali, Akbar; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Alam, Mohammad Mahtab; Mostafa, Mohamed S.; Kuznetsov, Aleksey","A synthetic approach towards drug modification: 2-hydroxy-1-naphthaldehyde based imine-zwitterion preparation, single-crystal study, Hirshfeld surface analysis, and computational investigation","RSC Advances","2024","14","10","6476","6493","10.1039/D3RA08727A","","","0.71073","MoKα","","0.1311","0.0763","","","0.2131","0.2358","","","","","","1.139","","","","has coordinates","289926","2024-02-22","02:35:09","" "7248210","9.3848","0.0003","13.2196","0.0005","19.2723","0.0006","79.837","0.003","79.503","0.002","84.025","0.002","2307.68","0.14","119.99","0.1","119.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C60 H34 N4 O4 S2 -","- C60 H34 N4 O4 S2 -","- C120 H68 N8 O8 S4 -","2","1","","Chen, Meiling; Chen, Yuzhuo; Li, Yan; Lin, Yuhong; Wu, Yunan","Efficient orange and red thermally activated delayed fluorescence materials based on 1,8-naphthalimide derivatives","RSC Advances","2024","14","10","6494","6500","10.1039/D3RA08969J","","x-ray","1.54184","CuKα","","0.0425","0.0385","","","0.1011","0.1048","","","","","","1.038","","","","has coordinates","289927","2024-02-22","02:35:27","" "7248211","10.9035","0.0004","16.1895","0.0006","24.4187","0.0017","102.495","0.005","95.298","0.004","105.416","0.003","4005.2","0.4","291.7","0.6","291.7","0.6","","","","","","","","4","P 1","P 1","1","","","","- C36 H24 N2 O2 -","- C36 H24 N2 O2 -","- C216 H144 N12 O12 -","6","6","","Chen, Meiling; Chen, Yuzhuo; Li, Yan; Lin, Yuhong; Wu, Yunan","Efficient orange and red thermally activated delayed fluorescence materials based on 1,8-naphthalimide derivatives","RSC Advances","2024","14","10","6494","6500","10.1039/D3RA08969J","","x-ray","1.54184","CuKα","","0.1625","0.1377","","","0.3838","0.4112","","","","","","1.384","","","","has coordinates","292638","2024-06-28","09:33:37","" "7248213","14.61601","0.00013","4.09391","0.00004","18.54407","0.00016","90","","100.646","0.0008","90","","1090.52","0.017","93.15","","93.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","methyl (R)-2-(5-bromopyridin-2-yl)-4,5-dihydrothiazole-4-carboxylate","","- C10 H9 Br N2 O2 S -","- C10 H9 Br N2 O2 S -","- C40 H36 Br4 N8 O8 S4 -","4","1","","Yano, Tetsuya; Yamada, Takahiro; Isida, Hiroaki; Ohashi, Nami; Itoh, Toshimasa","2-cyanopyridine derivatives enable N-terminal cysteine bioconjugation and peptide bond cleavage of glutathione under aqueous and mild conditions","RSC Advances","2024","14","10","6542","6547","10.1039/D4RA00437J","","x-ray","1.54184","CuKα","","0.0218","0.0218","","","0.0563","0.0563","","","","","","1.132","","","","has coordinates","289935","2024-02-23","02:25:05","" "7248232","8.7992","0.0002","16.6146","0.0004","16.7086","0.0004","119.195","0.002","91.698","0.002","102.782","0.002","2052.24","0.1","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C44 H44 B F4 Ir N4 O5 -","- C44 H44 B F4 Ir N4 O5 -","- C88 H88 B2 F8 Ir2 N8 O10 -","2","1","","Stokes, Emily C.; Shoetan, Ibrahim O.; Gillman, Alice M.; Horton, Peter N.; Coles, Simon J.; Woodbury, Simon E.; Fallis, Ian A.; Pope, Simon J. A.","Alkyl chain functionalised Ir(iii) complexes: synthesis, properties and behaviour as emissive dopants in microemulsions","RSC Advances","2024","14","10","6987","6997","10.1039/D3RA06764E","","x-ray","0.71075","MoKα","K-L~3~","0.0312","0.0264","","","0.0658","0.0674","","","","","","1.073","","","","has coordinates,has disorder","289978","2024-02-28","02:36:20","" "7248233","9.7337","0.0002","16.324","0.0003","18.6845","0.0004","100.368","0.002","91.4","0.002","104.629","0.002","2818.06","0.1","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","","","- C62 H68 B F4 Ir N5 O5.5 -","- C62 H68 B F4 Ir N5 O5.5 -","- C124 H136 B2 F8 Ir2 N10 O11 -","2","1","","Stokes, Emily C.; Shoetan, Ibrahim O.; Gillman, Alice M.; Horton, Peter N.; Coles, Simon J.; Woodbury, Simon E.; Fallis, Ian A.; Pope, Simon J. A.","Alkyl chain functionalised Ir(iii) complexes: synthesis, properties and behaviour as emissive dopants in microemulsions","RSC Advances","2024","14","10","6987","6997","10.1039/D3RA06764E","","x-ray","0.71075","MoKα","K-L~3~","0.0372","0.031","","","0.0758","0.0781","","","","","","1.045","","","","has coordinates,has disorder","289978","2024-02-28","02:36:21","" "7248234","3.8023","0.0002","17.9097","0.0009","15.9061","0.0008","90","","93.96","0.004","90","","1080.59","0.1","100","0.1","100","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C17 H9 N -","- C17 H9 N -","- C68 H36 N4 -","4","1","","Seki, Tomohiro; Hattori, Kota","Mechanochromic aromatic hydrocarbons that bear one simple substituent","RSC Advances","2024","14","11","7258","7262","10.1039/D3RA08519H","","x-ray","1.54184","CuKα","","0.0986","0.087","","","0.2486","0.2583","","","","","","1.12","","","","has coordinates","290016","2024-03-01","02:22:49","" "7248280","17.97496","0.0001","8.53541","0.00004","20.53738","0.0001","90","","92.6815","0.0005","90","","3147.47","0.03","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C29 H53 N P2 S2 -","- C29 H53 N P2 S2 -","- C116 H212 N4 P8 S8 -","4","1","","Hood, Thomas M.; Lau, Samantha; Chaplin, Adrian B.","Capture of mechanically interlocked molecules by rhodium-mediated terminal alkyne dimerisation","RSC Advances","2024","14","11","7740","7744","10.1039/D4RA00566J","","x-ray","1.54184","CuKα","","0.0266","0.0251","","","0.0636","0.0648","","","","","","1.037","","","","has coordinates","290353","2024-03-06","02:15:31","" "7248285","16.598","0.0005","18.4583","0.0006","20.9945","0.0007","74.614","0.003","75.671","0.003","74.331","0.003","5863","0.3","213","0.1","213","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C80 H167 N4 O36 S Ti10 -","- C80 H167 N4 O36 S Ti10 -","- C160 H334 N8 O72 S2 Ti20 -","2","1","","Nai, Haoran; Hou, Jinle; Li, Jinyu; Ma, Xiaoxi; Yang, Yujia; Qu, Konggang; Huang, Xianqiang; Li, Lianzhi","Accurate assembly of thiophene-bridged titanium-oxo clusters with photocatalytic amine oxidation activity","RSC Advances","2024","14","11","7924","7931","10.1039/D4RA00117F","","x-ray","1.54184","CuKα","","0.0796","0.0631","","","0.1663","0.1774","","","","","","1.04","","","","has coordinates,has disorder","290370","2024-03-07","02:17:26","" "7248286","9.6378","0.0001","13.1727","0.0001","10.2479","0.0001","90","","117.064","0.002","90","","1158.57","0.03","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C12 H3 F7 N2 O2 -","- C12 H3 F7 N2 O2 -","- C48 H12 F28 N8 O8 -","4","1","","Giri, Indrajit; Biswas, Sagar; Chhetri, Shant; Choudhuri, Anwesha; Mondal, Indrajit; Senanayak, Satyaprasad P.; Iyer, Parameswar Krishnan; Chaudhuri, Debangshu; Vijayaraghavan, Ratheesh K.","Ambient stable solution-processed organic field effect transistors from electron deficient planar aromatics: effect of end-groups on ambient stability","RSC Advances","2024","14","11","7915","7923","10.1039/D4RA01499E","","","1.54184","CuKα","","0.0367","0.0339","","","0.0924","0.0957","","","","","","1.052","","","","has coordinates","290371","2024-03-07","02:17:44","" "7248287","5.3597","0.0006","8.29","0.0008","15.7629","0.0008","99.995","0.006","93.825","0.007","95.201","0.008","684.48","0.11","100.01","0.13","100.01","0.13","","","","","","","","4","P -1","-P 1","2","","","","- C32.01 H34 N4 O4 -","- C32 H34 N4 O4 -","- C32 H34 N4 O4 -","1","0.5","","Giri, Indrajit; Biswas, Sagar; Chhetri, Shant; Choudhuri, Anwesha; Mondal, Indrajit; Senanayak, Satyaprasad P.; Iyer, Parameswar Krishnan; Chaudhuri, Debangshu; Vijayaraghavan, Ratheesh K.","Ambient stable solution-processed organic field effect transistors from electron deficient planar aromatics: effect of end-groups on ambient stability","RSC Advances","2024","14","11","7915","7923","10.1039/D4RA01499E","","x-ray","1.54184","CuKα","","0.1054","0.0986","","","0.306","0.322","","","","","","1.456","","","","has coordinates,has disorder","290371","2024-03-07","02:17:46","" "7248290","12.8165","0.0002","31.2237","0.0006","16.4633","0.0003","90","","102.225","0.001","90","","6438.9","0.2","98","2","98","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","CN-PAI-InCz","","- C86 H66 N8 O -","- C86 H66 N8 O -","- C344 H264 N32 O4 -","4","1","","Godi, Mahendra; Kwon, Hyukmin; Park, Sangwook; Park, Sunwoo; Lee, Hayoon; Lee, Kiho; Park, Jongwook","Enhancing OLED emitter efficiency through increased rigidity","RSC Advances","2024","14","12","8135","8144","10.1039/D3RA07937F","","","0.71073","MoKα","","0.0716","0.0468","","","0.1028","0.1147","","","","","","1.02","","","","has coordinates","290420","2024-03-09","02:22:12","" "7248295","21.402","0.0014","12.5878","0.0008","18.9598","0.0013","90","","123.154","0.003","90","","4276.3","0.5","101","2","101","2","","","","","","","","7","C 1 2 1","C 2y","5","","","","- C22 H21 Cl N4 O Ru S -","- C22 H21 Cl N4 O Ru S -","- C176 H168 Cl8 N32 O8 Ru8 S8 -","8","2","","Tsaulwayo, Nokwanda; Omondi, Reinner O.; Vijayan, Paranthaman; Sibuyi, Nicole R. S.; Meyer, Miché D.; Meyer, Mervin; Ojwach, Stephen O.","Heterocyclic (pyrazine)carboxamide Ru(ii) complexes: structural, experimental and theoretical studies of interactions with biomolecules and cytotoxicity","RSC Advances","2024","14","12","8322","8330","10.1039/D4RA00525B","","","0.71073","MoKα","","0.05","0.0476","","","0.1248","0.1265","","","","","","1.069","","","","has coordinates","290440","2024-03-12","02:20:46","" "7248296","17.9377","0.0011","21.9449","0.0014","25.6202","0.0016","90","","106.696","0.002","90","","9660","1.1","273","2","273.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C96 H72 Cd N24 O20 -","- C96 H72 Cd N24 O20 -","- C384 H288 Cd4 N96 O80 -","4","0.5","","Shi, Lulu; Wang, Lin; Li, Mingchun; Liu, Mei","A cucurbit[8]uril based supramolecular assembly and its potential applications for the removal of dye and antibiotic from an aqueous medium","RSC Advances","2024","14","12","8161","8166","10.1039/D4RA00347K","","","0.71073","MoKα","","0.0388","0.0354","","","0.0855","0.0915","","","","","","1.112","","","","has coordinates","290441","2024-03-12","02:21:47","" "7248297","8.867","0.0001","7.143","0.0001","22.2918","0.0003","90","","90.537","0.001","90","","1411.83","0.03","100","2","100","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C15 H19 N5 -","- C15 H19 N5 -","- C60 H76 N20 -","4","1","","Bin Shahari, Muhammad Syafiq; Junaid, Ahmad; Tiekink, Edward R. T.; Dolzhenko, Anton V.","6-Aryl-4-cycloamino-1,3,5-triazine-2-amines: synthesis, antileukemic activity, and 3D-QSAR modelling","RSC Advances","2024","14","12","8264","8282","10.1039/D3RA08091A","","","1.54184","CuKα","","0.0397","0.0381","","","0.1033","0.1051","","","","","","1.055","","","","has coordinates","290442","2024-03-12","02:22:02","" "7248316","20.8238","0.0019","15.3516","0.0014","13.7001","0.0014","90","","90","","90","","4379.6","0.7","150","2","150","2","","","","","","","synthesis as described","6","C m c e","-C 2ac 2","64","","","","- C16 H20 Br4 Hg N2 O2 -","- C16 H20 Br4 Hg N2 O2 -","- C128 H160 Br32 Hg8 N16 O16 -","8","0.5","","Chkoundali, Souad; Garoui, Iheb; Trigui, Wala; Oueslati, Abderrazek","Crystal structure, Hirshfeld surface analysis, conduction mechanism and electrical modulus study of the new organic-inorganic compound [C8H10NO]2HgBr4.","RSC advances","2024","14","13","8971","8980","10.1039/d4ra00689e","","x-ray","0.71073","MoKα","","0.0168","0.015","","","0.0345","0.0352","","","","","","1.113","","","","has coordinates","290535","2024-03-19","03:00:53","" "7248332","14.6984","0.0008","17.427","0.0008","19.6342","0.001","90","","90","","90","","5029.3","0.4","296","2","296","2","","","","","","","","6","P 21 21 2","P 2 2ab","18","","","","- C24 H28 Cl N3 O6 S -","- C24 H28 Cl N3 O6 S -","- C192 H224 Cl8 N24 O48 S8 -","8","2","","Parmar, Mehul P.; Vala, Disha P.; Bhalodiya, Savan S.; Upadhyay, Dipti B.; Patel, Chirag D.; Patel, Subham G.; Gandholi, Srinivasa R.; Shaik, Althaf H.; Miller, Amy Dunne; Nogales, Joaquina; Banerjee, Sourav; Padrón, José M; Amri, Nasser; Kandukuri, Nagesh Kumar; Patel, Hitendra M.","A green bio-organic catalyst (taurine) promoted one-pot synthesis of (R/S)-2-thioxo-3,4-dihydropyrimidine(TDHPM)-5-carboxanilides: chiral investigations using circular dichroism and validation by computational approaches.","RSC advances","2024","14","13","9300","9313","10.1039/d4ra01391c","","","0.71073","MoKα","","0.1428","0.0619","","","0.1158","0.1453","","","","","","1.078","","","","has coordinates","290573","2024-03-21","02:14:56","" "7248333","11.9361","0.0003","7.3938","0.0002","14.4601","0.0004","90","","93.592","0.001","90","","1273.64","0.06","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","1-(2,5-dihydroxyphenyl)-4-ethylpyridin-1-ium chloride water solvate","","- C13 H16 Cl N O3 -","- C13 H16 Cl N O3 -","- C52 H64 Cl4 N4 O12 -","4","1","","Zgheib, Ali; Acker, Sophie; Fischer, Maximilian Hans; Namyslo, Jan C.; Strube, Franziska; Rudolph, Martin; Fittschen, Ursula E. A.; Wollmann, Annett; Weber, Alfred P.; Nieger, Martin; Schmidt, Andreas","Lithium aluminate flotation by pH- and light-switchable collectors based on the natural product punicine","RSC Advances","2024","14","13","9353","9364","10.1039/D4RA00116H","","","0.71073","MoKα","","0.0315","0.0297","","","0.0811","0.0826","","","","","","1.052","","","","has coordinates","290574","2024-03-21","02:15:15","" "7248339","7.5716","0.0002","10.5701","0.0003","13.3435","0.0004","81.216","0.002","83.633","0.002","76.137","0.002","1021.57","0.05","100","","100","","","","","","","","","6","P -1","-P 1","2","","","","- C23 H17 F3 N2 O3 S -","- C23 H17 F3 N2 O3 S -","- C46 H34 F6 N4 O6 S2 -","2","1","","Kawakubo, Masato; Inoh, Yoshikazu; Murata, Yuki; Matsumura, Mio; Furuno, Tadahide; Yasuike, Shuji","Novel mono substituted pyridoimidazoisoquinoliniums via a silver-catalyzed intramolecular cyclization and their applications in cellular imaging","RSC Advances","2024","14","14","9758","9762","10.1039/D4RA01210K","","x-ray","1.54184","CuKα","","0.0382","0.0367","","","0.0971","0.0986","","","","","","1.07","","","","has coordinates","290625","2024-03-24","02:10:59","" "7248353","23.125","0.002","10.9006","0.001","13.78","0.0014","90","","123.111","0.003","90","","2909.5","0.5","100","","100","","","","","","","","see text","6","C 1 2/c 1","-C 2yc","15","","PdL13","","- C20 H36 F12 N8 P2 Pd -","- C20 H36 F12 N8 P2 Pd -","- C80 H144 F48 N32 P8 Pd4 -","4","0.5","","Büchele, Wolfgang R. E.; Schlachta, Tim P.; Gebendorfer, Andreas L.; Pamperin, Jenny; Richter, Leon F.; Sauer, Michael J.; Prokop, Aram; Kühn, Fritz E.","Synthesis, characterization, and biomedical evaluation of ethylene-bridged tetra-NHC Pd(ii), Pt(ii) and Au(iii) complexes, with apoptosis-inducing properties in cisplatin-resistant neuroblastoma cells","RSC Advances","2024","14","15","10244","10254","10.1039/D4RA01195C","","x-ray","0.71073","MoKα","","0.0334","0.0269","","","0.0544","0.0579","","","","","","1.072","","","","has coordinates,has disorder","290694","2024-03-28","02:27:01","" "7248354","13.4513","0.0006","13.4513","0.0006","16.2016","0.0013","90","","90","","90","","2931.5","0.3","100","","100","","","","","","","","see text","6","P 4/n c c :2","-P 4a 2ac","130","","PdL15","","- C20 H24 F12 N8 P2 Pd -","- C20 H24 F12 N8 P2 Pd -","- C80 H96 F48 N32 P8 Pd4 -","4","0.25","","Büchele, Wolfgang R. E.; Schlachta, Tim P.; Gebendorfer, Andreas L.; Pamperin, Jenny; Richter, Leon F.; Sauer, Michael J.; Prokop, Aram; Kühn, Fritz E.","Synthesis, characterization, and biomedical evaluation of ethylene-bridged tetra-NHC Pd(ii), Pt(ii) and Au(iii) complexes, with apoptosis-inducing properties in cisplatin-resistant neuroblastoma cells","RSC Advances","2024","14","15","10244","10254","10.1039/D4RA01195C","","x-ray","0.71073","MoKα","","0.0342","0.0238","","","0.0524","0.0565","","","","","","1.074","","","","has coordinates","290694","2024-03-28","02:27:11","" "7248355","23.0841","0.0018","10.8943","0.0008","13.7057","0.0011","90","","122.799","0.002","90","","2897.3","0.4","100","","100","","","","","","","","see text","6","C 1 2/c 1","-C 2yc","15","","PtL13","","- C20 H36 F12 N8 P2 Pt -","- C20 H36 F12 N8 P2 Pt -","- C80 H144 F48 N32 P8 Pt4 -","4","0.5","","Büchele, Wolfgang R. E.; Schlachta, Tim P.; Gebendorfer, Andreas L.; Pamperin, Jenny; Richter, Leon F.; Sauer, Michael J.; Prokop, Aram; Kühn, Fritz E.","Synthesis, characterization, and biomedical evaluation of ethylene-bridged tetra-NHC Pd(ii), Pt(ii) and Au(iii) complexes, with apoptosis-inducing properties in cisplatin-resistant neuroblastoma cells","RSC Advances","2024","14","15","10244","10254","10.1039/D4RA01195C","","x-ray","0.71073","MoKα","","0.0161","0.0138","","","0.0293","0.0304","","","","","","1.167","","","","has coordinates,has disorder","290694","2024-03-28","02:27:12","" "7248356","31.7839","0.0012","5.0577","0.0002","26.4285","0.0011","90","","90","","90","","4248.5","0.3","299","","299","","","","","","","","","4","P c a 21","P 2c -2ac","29","","","","- C25 H16 N2 O4 -","- C26 H20 N2 O5 -","- C208 H160 N16 O40 -","8","2","","Polo-Cuadrado, Efraín; Osorio, Edison; Acosta-Quiroga, Karen; Camargo-Ayala, Paola Andrea; Brito, Iván; Rodriguez, Jany; Alderete, Joel B.; Forero-Doria, Oscar; Blanco-Acuña, Edgard Fabián; Gutiérrez, Margarita","Nonlinear optical and spectroscopic properties, thermal analysis, and hemolytic capacity evaluation of quinoline-1,3-benzodioxole chalcone","RSC Advances","2024","14","15","10199","10208","10.1039/D4RA00820K","","","0.71073","MoKα","","0.0779","0.0558","","","0.1414","0.1607","","","","","","1.121","","","","has coordinates","290695","2024-03-28","02:27:34","" "7248364","6.5671","0.001","7.2171","0.0011","14.364","0.002","85.588","0.004","81.019","0.004","83.178","0.004","666.5","0.17","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H9 F3 O2 S -","- C16 H9 F3 O2 S -","- C32 H18 F6 O4 S2 -","2","1","","Mukhtar, Asma; Hussain, Arif; Younas, Faiza; Yousuf, Sammer; Saeed, Muhammad","Facile synthesis of substituted 2-aroylbenzo[b]thiophen-3-ols to form novel triazole hybrids using click chemistry","RSC Advances","2024","14","15","10270","10279","10.1039/D4RA01146E","","","1.54178","CuKα","","0.0418","0.041","","","0.1305","0.1316","","","","","","1.275","","","","has coordinates","290709","2024-03-29","02:22:04","" "7248372","17.7833","0.0012","17.8696","0.0012","18.2588","0.0012","110.766","0.002","112.206","0.002","90.922","0.002","4946.9","0.6","170","","170","","","","","","","","","8","P -1","-P 1","2","","","","- C96 H64 Ag4 Br3.69 Cl8.62 P2 Pt S8 -","- C96 H64 Ag4 Br3.69 Cl8.62 P2 Pt S8 -","- C192 H128 Ag8 Br7.38 Cl17.24 P4 Pt2 S16 -","2","1","","Jiang, Kefan; Ma, Along; Li, Yuansheng; Wang, Jiawei; Yin, Zhengmao; Wang, Shuxin","Understanding the decomposition process of the Pt1Ag24(SPhCl2)18 nanocluster at the atomic level","RSC Advances","2024","14","15","10574","10579","10.1039/D4RA01274G","","","0.71073","MoKα","","0.1436","0.0994","","","0.2393","0.2635","","","","","","1.058","","","","has coordinates,has disorder","290745","2024-04-03","01:32:17","" "7248373","32.937","","28.819","","28.779","","90","","93.52","","90","","27265.8","","120.15","","120.15","","","","","","","","","8","C 1 2/c 1","-C 2yc","15","","","","- C216 H134 Ag24 Br17.72 Cl4.56 P4 Pt S20 -","- C216 H134 Ag24 Br17.72 Cl4.56 P4 Pt S20 -","- C864 H536 Ag96 Br70.88 Cl18.24 P16 Pt4 S80 -","4","0.5","","Jiang, Kefan; Ma, Along; Li, Yuansheng; Wang, Jiawei; Yin, Zhengmao; Wang, Shuxin","Understanding the decomposition process of the Pt1Ag24(SPhCl2)18 nanocluster at the atomic level","RSC Advances","2024","14","15","10574","10579","10.1039/D4RA01274G","","","1.54186","CuKα","","0.0851","0.0561","","","0.1403","0.1526","","","","","","0.946","","","","has coordinates,has disorder","290745","2024-04-03","01:32:17","" "7248374","26.638","","29.956","","31.053","","93.09","","90.67","","90.79","","24739","","120","","120","","","","","","","","","8","P -1","-P 1","2","","","","- C184 H120.67 Ag24 Br12.49 Cl15.03 P2.67 Pt S20 -","- C184 H120.667 Ag24 Br12.4867 Cl15.0267 P2.66667 Pt S20 -","- C552 H362 Ag72 Br37.46 Cl45.08 P8 Pt3 S60 -","3","1.5","","Jiang, Kefan; Ma, Along; Li, Yuansheng; Wang, Jiawei; Yin, Zhengmao; Wang, Shuxin","Understanding the decomposition process of the Pt1Ag24(SPhCl2)18 nanocluster at the atomic level","RSC Advances","2024","14","15","10574","10579","10.1039/D4RA01274G","","x-ray","1.54186","CuKα","","0.0909","0.0607","","","0.165","0.185","","","","","","1.041","","","","has coordinates,has disorder","290745","2024-04-03","01:32:17","" "7248375","10.0589","0.0002","14.2921","0.0003","15.1181","0.0003","90","","90","","90","","2173.42","0.08","99.8","0.7","99.8","0.7","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","Compound 19","","- C25 H34 O5 -","- C25 H34 O5 -","- C100 H136 O20 -","4","1","","Ma, Chi Thanh; Huang, Tianqi; Yu, Jae Sik; Ly, Tu Loan; Vu Huynh, Kim Long; Kwon, Sung Won; Park, Jeong Hill; Yang, Hyun Ok","Sesquiterpenoids and hexanorcucurbitacin from Aquilaria malaccensis agarwood with anti-inflammatory effects by inhibiting the STAT1/AKT/MAPK/NLRP3 pathway","RSC Advances","2024","14","13","9391","9405","10.1039/D3RA08686K","","x-ray","1.54184","CuKα","","0.0382","0.0369","","","0.0976","0.0987","","","","","","1.067","","","","has coordinates","290746","2024-04-03","01:32:38","" "7248376","6.7814","0.0004","10.688","0.0007","29.8384","0.0018","90","","94.276","0.003","90","","2156.7","0.2","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H26 N2 O -","- C26 H26 N2 O -","- C104 H104 N8 O4 -","4","1","","Shalaby, Mona A.; BinSabt, Mohammad H.; Rizk, Sameh A.; Fahim, Asmaa M.","Novel pyrazole and imidazolone compounds: synthesis, X-ray crystal structure with theoretical investigation of new pyrazole and imidazolone compounds anticipated insecticide’s activities against targeting Plodia interpunctella and nilaparvata lugens","RSC Advances","2024","14","15","10464","10480","10.1039/D4RA00602J","","","1.54178","CuKα","","0.0469","0.0398","","","0.1176","0.1251","","","","","","1.059","","","","has coordinates","290747","2024-04-03","01:32:51","" "7248391","10.105","0.004","7.746","0.003","15.032","0.008","90","","91.13","0.03","90","","1176.4","0.9","293","","293","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","DMSS-AM","","","- C22 H36 N4 O6 -","- C22 H34 N4 O6 -","- C44 H68 N8 O12 -","2","0.5","","Jin, Yuxin; Jiang, Bingli; Song, Huajian; Mei, Chanming; Liu, Zuoan; Zhang, Xiakai; Liu, Jinyuan; Gong, Yongyang","Monophenyl luminescent material with dual-state emission and pH sensitivity for cell imaging.","RSC advances","2024","14","16","10942","10952","10.1039/d4ra01422g","","","1.54178","CuKα","","0.1028","0.0701","","","0.1893","0.2109","","","","","","1.106","","","","has coordinates","291133","2024-04-06","01:30:32","" "7248392","9.8989","0.0003","11.368","0.0003","15.8912","0.0005","90","","90","","90","","1788.25","0.09","150","2","150","2","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C20 H22 O7 -","- C20 H22 O7 -","- C80 H88 O28 -","4","1","","Zhang, Xiao-Fang; Du, Jiao-Xian; Teng, Si-Qiong; Liu, Hui; He, Juan; Feng, Tao; Liu, Ji-Kai","Carpesabrolide A, a novel meroterpenoid with anti-inflammatory activity from Carpesium abrotanoides","RSC Advances","2024","14","16","11002","11006","10.1039/D4RA00292J","","","1.54178","CuKα","","0.031","0.0295","","","0.0723","0.0731","","","","","","1.057","","","","has coordinates","291134","2024-04-06","01:30:46","" "7248393","21.066","0.008","12.519","0.007","17.232","0.008","90","","90","","90","","4545","4","293","2","293","2","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C39 H52 Co3 N16 O5 -","- C38 H48 Co3 N16 O4 -","- C152 H192 Co12 N64 O16 -","4","1","","Bhunia, Sudip; Das, Mainak; Banerjee, Snehasis; Drew, Michael. G. B.; Ray, Partha Pratim; Chattopadhyay, Shouvik","Application of a distinctly bent, trinuclear, end-to-end azide bridged, mixed valence cobalt(iii/ii/iii) complex in the fabrication of photosensitive Schottky barrier diodes","RSC Advances","2024","14","16","11185","11196","10.1039/D4RA01406E","","","0.71073","MoKα","","0.0976","0.0604","","","0.0913","0.1059","","","","","","1.0454","","","","has coordinates","291142","2024-04-09","01:14:29","" "7248395","24.6697","0.0019","13.3392","0.001","15.2344","0.0009","90","","115.878","0.004","90","","4510.5","0.6","170","2","170","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C18 H24 Co N10 S2 -","- C18 H24 Co N10 S2 -","- C144 H192 Co8 N80 S16 -","8","1","","Hannachi, Anissa; El Bakri, Youness; Saravanan, Kandasamy; Gómez-García, Carlos J.; Abuelizz, Hatem A.; Al-Salahi, Rashad; Smirani, Wajda","Metamagnetism and canted antiferromagnetic ordering in two monomeric CoII complexes with 1-(2-pyrimidyl)piperazine. Hirshfeld surface analysis and theoretical studies","RSC Advances","2024","14","16","11557","11569","10.1039/D4RA00716F","","","0.71073","MoKα","","0.1149","0.0615","","","0.0966","0.1111","","","","","","1.04","","","","has coordinates","291174","2024-04-11","01:25:08","" "7248396","16.4142","0.0003","16.5691","0.0004","15.1392","0.0004","90","","90","","90","","4117.39","0.17","170","2","170","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C12 H16 Co N8 O S4 -","- C12 H16 Co N8 O S4 -","- C96 H128 Co8 N64 O8 S32 -","8","2","","Hannachi, Anissa; El Bakri, Youness; Saravanan, Kandasamy; Gómez-García, Carlos J.; Abuelizz, Hatem A.; Al-Salahi, Rashad; Smirani, Wajda","Metamagnetism and canted antiferromagnetic ordering in two monomeric CoII complexes with 1-(2-pyrimidyl)piperazine. Hirshfeld surface analysis and theoretical studies","RSC Advances","2024","14","16","11557","11569","10.1039/D4RA00716F","","","0.71073","MoKα","","0.0796","0.0493","","","0.0778","0.0859","","","","","","1.03","","","","has coordinates","291174","2024-04-11","01:25:10","" "7248416","14.6897","0.0005","14.0457","0.0006","20.6528","0.0007","90","","104.441","0.001","90","","4126.6","0.3","120","2","120","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C28 H19 Br O2 -","- C28 H19 Br O2 -","- C224 H152 Br8 O16 -","8","2","","Silber, Vincent; Gourlaouen, Christophe; Ruppert, Romain","Keto–enol equilibrium: stable tautomers of ortho-, meta-, and para-hydroquinones in large aromatics","RSC Advances","2024","14","17","11969","11976","10.1039/D4RA02202E","","","0.71073","MoKα","","0.0389","0.0295","","","0.0709","0.0764","","","","","","1.006","","","","has coordinates","291219","2024-04-16","01:33:25","" "7248417","10.168","0.002","10.859","0.002","11.191","0.002","82.43","0.03","64.17","0.03","76.64","0.03","1081.4","0.5","","","","","","","","","","","","4","P -1","-P 1","2","","","","- C26 H34 N2 O2 -","- C26 H34 N2 O2 -","- C52 H68 N4 O4 -","2","1","","Tian, Feng-Xian; Liu, Fan-Fan; Wei, Jian; Xiao, Jia-Xi; Qu, Jin","Redox-neutral α-functionalization of pyrrolidines: facile access to α-aryl-substituted pyrrolidines","RSC Advances","2024","14","17","11986","11991","10.1039/D4RA00983E","","","","","","0.058","","","","","","","","","","","","","","","has coordinates","291220","2024-04-16","01:33:40","" "7248418","8.1861","0.0011","11.0003","0.0016","14.636","0.002","76.208","0.005","78.404","0.004","86.588","0.004","1253.7","0.3","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C32 H26 N2 O3 -","- C32 H26 N2 O3 -","- C64 H52 N4 O6 -","2","1","","Alkaltham, Manal Fahad; Almansour, Abdulrahman I.; Arumugam, Natarajan; Vagolu, Siva Krishna; Tønjum, Tone; Alaqeel, Shatha Ibrahim; Rajaratnam, Saiswaroop; Sivaramakrishnan, Venketesh","Activity against Mycobacterium tuberculosis of a new class of spirooxindolopyrrolidine embedded chromanone hybrid heterocycles.","RSC advances","2024","14","17","11604","11613","10.1039/d4ra01501k","","","0.71073","MoKα","","0.1243","0.0521","","","0.0963","0.1183","","","","","","1.034","","","","has coordinates","291221","2024-04-16","01:34:11","" "7248419","10.392","0.002","11.038","0.002","13.93","0.003","66.842","0.006","83.821","0.008","68.789","0.006","1368.5","0.5","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C33 H28 N2 O4 -","- C33 H28 N2 O4 -","- C66 H56 N4 O8 -","2","1","","Alkaltham, Manal Fahad; Almansour, Abdulrahman I.; Arumugam, Natarajan; Vagolu, Siva Krishna; Tønjum, Tone; Alaqeel, Shatha Ibrahim; Rajaratnam, Saiswaroop; Sivaramakrishnan, Venketesh","Activity against Mycobacterium tuberculosis of a new class of spirooxindolopyrrolidine embedded chromanone hybrid heterocycles.","RSC advances","2024","14","17","11604","11613","10.1039/d4ra01501k","","","0.71073","MoKα","","0.0744","0.0471","","","0.104","0.1181","","","","","","1.008","","","","has coordinates","291221","2024-04-16","01:34:11","" "7248420","36.4386","0.0008","9.7054","0.0003","30.3886","0.0007","90","","110.431","0.001","90","","10070.9","0.5","194","","194","","","","","","","","","3","C 1 2/c 1","-C 2yc","15","BPQ","Bis(pyreneloquinoxaline)","","- C64 H60 N4 -","- C64 H60 N4 -","- C512 H480 N32 -","8","1","","Zhang, Dongyang; Zhang, Fengyuan; Du, Hanyun; Liu, Fei; Yi, Xiaohui; Chen, Jun; Hu, Ben-Lin","U-shaped stereoscopic design strategy toward N-doped nanographene segment.","RSC advances","2024","14","17","11771","11774","10.1039/d4ra00788c","","x-ray","1.54178","CuKα","","0.1057","0.0711","","","0.193","0.231","","","","","","1.075","","","","has coordinates,has disorder","291222","2024-04-16","01:34:34","" "7248423","10.1753","0.0002","10.828","0.0002","18.8802","0.0003","102.097","0.002","99.993","0.002","106.014","0.002","1894.91","0.07","293","2","180.15","","","","","","","","","4","P -1","-P 1","2","","","","- C46 H40 N4 O4 -","- C46 H40 N4 O4 -","- C92 H80 N8 O8 -","2","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","","1.54184","CuKα","","0.0427","0.0375","","","0.1012","0.1042","","","","","","1.062","","","","has coordinates,has disorder","291248","2024-04-17","01:39:07","" "7248424","10.57556","0.00011","33.1193","0.0003","9.47501","0.0001","90","","98.5987","0.001","90","","3281.37","0.06","149.98","0.16","149.98","0.16","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C38 H28 N4 O3 -","- C38 H28 N4 O3 -","- C152 H112 N16 O12 -","4","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","x-ray","1.54184","CuKα","","0.0475","0.0443","","","0.1296","0.1324","","","","","","1.031","","","","has coordinates","291248","2024-04-17","01:39:09","" "7248425","14.20645","0.00012","9.47536","0.00007","21.65599","0.00018","90","","91.4501","0.0007","90","","2914.21","0.04","180","0.16","180","0.16","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C32 H28 Cl2 N4 O3 -","- C32 H28 Cl2 N4 O3 -","- C128 H112 Cl8 N16 O12 -","4","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","x-ray","1.54184","CuKα","","0.0588","0.0568","","","0.1529","0.1545","","","","","","1.044","","","","has coordinates","291248","2024-04-17","01:39:18","" "7248426","29.7627","0.0004","9.05888","0.00012","18.3792","0.0002","90","","92.1028","0.0012","90","","4952","0.11","179.99","0.1","179.99","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C30 H23 F N4 O2 -","- C30 H23 F N4 O2 -","- C240 H184 F8 N32 O16 -","8","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","x-ray","1.54184","CuKα","","0.0375","0.0334","","","0.0892","0.0916","","","","","","1.051","","","","has coordinates","291248","2024-04-17","01:39:35","" "7248427","13.693","0.0003","26.2789","0.0005","16.4539","0.0004","90","","102.605","0.002","90","","5778","0.2","149.99","0.14","149.99","0.14","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C65 H48 Cl4 N8 O6 Pd2 -","- C65 H48 Cl4 N8 O6 Pd2 -","- C260 H192 Cl16 N32 O24 Pd8 -","4","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","","1.54184","CuKα","","0.0762","0.0549","","","0.1371","0.1477","","","","","","1.053","","","","has coordinates,has disorder","291248","2024-04-17","01:39:36","" "7248428","30.8184","0.0004","8.96166","0.00012","18.6116","0.0002","90","","94.5518","0.0012","90","","5124.01","0.11","179.98","0.1","179.98","0.1","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C31 H26 N4 O2 -","- C31 H26 N4 O2 -","- C248 H208 N32 O16 -","8","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","x-ray","1.54184","CuKα","","0.0443","0.0373","","","0.0982","0.1017","","","","","","1.049","","","","has coordinates","291248","2024-04-17","01:39:44","" "7248429","11.6496","0.0002","14.1847","0.0002","22.6036","0.0003","105.402","0.001","90.354","0.001","107.05","0.002","3428.4","0.1","179.97","0.14","179.97","0.14","","","","","","","","4","P -1","-P 1","2","","","","- C80 H74 N8 O11 -","- C80 H74 N8 O11 -","- C160 H148 N16 O22 -","2","1","","Antoniou, Ioakeim M.; Ioannou, Natalia; Panagiotou, Nikos; Georgiades, Savvas N.","LED-induced Ru-photoredox Pd-catalyzed C–H arylation of (6-phenylpyridin-2-yl)pyrimidines and heteroaryl counterparts","RSC Advances","2024","14","17","12179","12191","10.1039/D4RA02173H","","x-ray","1.54184","CuKα","","0.0437","0.0392","","","0.103","0.1058","","","","","","1.06","","","","has coordinates,has disorder","291248","2024-04-17","01:40:01","" "7248430","8.928","0.004","13.417","0.007","20.372","0.007","100.79","0.02","95.217","0.017","100.557","0.016","2336.7","1.8","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C51 H39 Cl3 N2 O12 -","- C51 H39 Cl3 N2 O12 -","- C102 H78 Cl6 N4 O24 -","2","1","","Benny, Anjitha Theres; Thamim, Masthan; Srivastava, Prakhar; Suresh, Sindoora; Thirumoorthy, Krishnan; Rangasamy, Loganathan; S., Karthikeyan; Easwaran, Nalini; Radhakrishnan, Ethiraj Kannatt","Synthesis and study of antibiofilm and antivirulence properties of flavonol analogues generated by palladium catalyzed ligand free Suzuki–Miyaura coupling against Pseudomonas aeruginosa PAO1","RSC Advances","2024","14","18","12278","12293","10.1039/D3RA08617H","","","1.54184","CuKα","","0.1051","0.0734","","","0.184","0.2071","","","","","","1.035","","","","has coordinates,has disorder","291249","2024-04-17","01:41:00","" "7248431","8.8256","0.0016","12.078","0.002","13.533","0.002","105.526","0.006","98.35","0.006","106.79","0.006","1291.4","0.4","300","2","300","2","","","","","","","","4","P -1","-P 1","2","","","","- C26 H23 Cl3 O7 -","- C26 H23 Cl3 O7 -","- C52 H46 Cl6 O14 -","2","1","","Benny, Anjitha Theres; Thamim, Masthan; Srivastava, Prakhar; Suresh, Sindoora; Thirumoorthy, Krishnan; Rangasamy, Loganathan; S., Karthikeyan; Easwaran, Nalini; Radhakrishnan, Ethiraj Kannatt","Synthesis and study of antibiofilm and antivirulence properties of flavonol analogues generated by palladium catalyzed ligand free Suzuki–Miyaura coupling against Pseudomonas aeruginosa PAO1","RSC Advances","2024","14","18","12278","12293","10.1039/D3RA08617H","","","0.71073","MoKα","","0.0937","0.0632","","","0.1421","0.1637","","","","","","1.028","","","","has coordinates","291249","2024-04-17","01:41:01","" "7248432","11.47661","0.00014","17.9492","0.0002","17.0666","0.0003","90","","92.1926","0.0012","90","","3513.08","0.08","140","0.1","140","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C43 H34 O2 P2 Pt Se -","- C43 H34 O2 P2 Pt Se -","- C172 H136 O8 P8 Pt4 Se4 -","4","1","","Atiga, Simeon; Saunders, Graham C.; Henderson, William","Selenosalicylate; a little-studied heavy-element analogue of the versatile thiosalicylate ligand","RSC Advances","2024","14","18","12323","12336","10.1039/D4RA00926F","","x-ray","1.54184","CuKα","","0.0291","0.0237","","","0.0548","0.0574","","","","","","1.0462","","","","has coordinates,has disorder","291250","2024-04-17","01:42:28","" "7248433","9.5935","0.0003","12.8922","0.0003","12.4357","0.0005","90","","106.07","0.003","90","","1477.96","0.09","100","0.2","100","0.2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C34 H36 O4 Ru2 Se2 -","- C34 H36 O4 Ru2 Se2 -","- C68 H72 O8 Ru4 Se4 -","2","0.5","","Atiga, Simeon; Saunders, Graham C.; Henderson, William","Selenosalicylate; a little-studied heavy-element analogue of the versatile thiosalicylate ligand","RSC Advances","2024","14","18","12323","12336","10.1039/D4RA00926F","","x-ray","1.54184","CuKα","","0.0279","0.0245","","","0.0611","0.0637","","","","","","1.0387","","","","has coordinates","291250","2024-04-17","01:42:30","" "7248434","11.2452","0.00015","10.02131","0.00011","14.11953","0.00018","90","","99.208","0.0013","90","","1570.65","0.03","140","0.1","140","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C34 H38 O4 Rh2 Se2 -","- C34 H38 O4 Rh2 Se2 -","- C68 H76 O8 Rh4 Se4 -","2","0.5","","Atiga, Simeon; Saunders, Graham C.; Henderson, William","Selenosalicylate; a little-studied heavy-element analogue of the versatile thiosalicylate ligand","RSC Advances","2024","14","18","12323","12336","10.1039/D4RA00926F","","x-ray","1.54184","CuKα","","0.0305","0.0235","","","0.051","0.0532","","","","","","1.0342","","","","has coordinates","291250","2024-04-17","01:42:48","" "7248435","8.6583","0.0003","18.2265","0.0006","19.3876","0.0006","86.012","0.003","86.316","0.002","82.18","0.003","3019.12","0.17","99.9","0.5","99.9","0.5","","","","","","","","6","P -1","-P 1","2","","","","- C70 H70 Ir2 O5 P2 Se2 -","- C70 H70 Ir2 O5 P2 Se2 -","- C140 H140 Ir4 O10 P4 Se4 -","2","1","","Atiga, Simeon; Saunders, Graham C.; Henderson, William","Selenosalicylate; a little-studied heavy-element analogue of the versatile thiosalicylate ligand","RSC Advances","2024","14","18","12323","12336","10.1039/D4RA00926F","","x-ray","1.54184","CuKα","","0.0369","0.0323","","","0.0685","0.071","","","","","","1.0508","","","","has coordinates,has disorder","291250","2024-04-17","01:42:50","" "7248513","10.4218","0.0004","10.9812","0.0004","12.6764","0.0004","104.684","0.001","97.921","0.001","100.105","0.001","1356.04","0.08","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C44 H60 Cl2 Co3 N4 O27 -","- C44 H60 Cl2 Co3 N4 O27 -","- C44 H60 Cl2 Co3 N4 O27 -","1","0.5","","Maity, Sovana; Bhunia, Sudip; Drew, Michael G. B.; Gomila, Rosa M.; Frontera, Antonio; Chattopadhyay, Shouvik","Formation of H-bonding networks in the solid state structure of a trinuclear cobalt(iii/ii/iii) complex with N2O2 donor Schiff base ligand and glutaric acid as bridging co-ligand: synthesis, structure and DFT study","RSC Advances","2024","14","19","13200","13208","10.1039/D3RA07697K","","","0.71073","MoKα","","0.0471","0.0424","","","0.1071","0.1101","","","","","","1.293","","","","has coordinates,has disorder","291343","2024-04-24","01:02:14","" "7248514","10.5977","0.0005","10.9118","0.0005","11.3038","0.0005","70.094","0.002","79.697","0.002","80.099","0.002","1200.51","0.1","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H29 N3 O2 Pt -","- C27 H29 N3 O2 Pt -","- C54 H58 N6 O4 Pt2 -","2","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.0139","0.0126","","","0.031","0.0316","","","","","","1.03","","","","has coordinates","291344","2024-04-24","01:03:01","" "7248515","9.8997","0.0003","13.5956","0.0004","18.9893","0.0005","90","","99.627","0.002","90","","2519.82","0.13","293","2","293","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 Br3 N3 O2 Pt -","- C24 H20 Br3 N3 O2 Pt -","- C96 H80 Br12 N12 O8 Pt4 -","4","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.1424","0.069","","","0.1604","0.2107","","","","","","0.932","","","","has coordinates","291344","2024-04-24","01:03:02","" "7248516","23.563","0.0005","5.2983","0.0001","18.4229","0.0003","90","","90","","90","","2299.99","0.08","293","2","293","2","","","","","","","","6","P c a 21","P 2c -2ac","29","","","","- C24 H20 F3 N3 O2 Pt -","- C24 H20 F3 N3 O2 Pt -","- C96 H80 F12 N12 O8 Pt4 -","4","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.0385","0.0357","","","0.0796","0.0813","","","","","","1.079","","","","has coordinates,has disorder","291344","2024-04-24","01:03:02","" "7248517","10.8336","0.0005","10.9407","0.0006","12.9074","0.0005","75.575","0.004","88.599","0.004","70.372","0.004","1392.61","0.12","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C30 H35 N3 O2 Pt -","- C30 H35 N3 O2 Pt -","- C60 H70 N6 O4 Pt2 -","2","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.0649","0.0486","","","0.1007","0.1093","","","","","","1.049","","","","has coordinates","291344","2024-04-24","01:03:02","" "7248518","9.6602","0.0003","13.4897","0.0004","18.9814","0.0006","90","","99.169","0.003","90","","2441.92","0.13","298","2","298","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C24 H20 Cl3 N3 O2 Pt -","- C24 H20 Cl3 N3 O2 Pt -","- C96 H80 Cl12 N12 O8 Pt4 -","4","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.0632","0.046","","","0.1063","0.1141","","","","","","1.049","","","","has coordinates","291344","2024-04-24","01:03:02","" "7248519","10.2195","0.0004","10.2608","0.0005","21.3421","0.0008","90","","90.459","0.003","90","","2237.87","0.16","298","2","298","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C24 H20 F3 N3 O2 Pt -","- C24 H20 F3 N3 O2 Pt -","- C96 H80 F12 N12 O8 Pt4 -","4","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.0473","0.0387","","","0.0844","0.0899","","","","","","1.095","","","","has coordinates","291344","2024-04-24","01:03:02","" "7248520","9.9894","0.0003","22.7931","0.0007","11.6752","0.0003","90","","93.968","0.003","90","","2651.95","0.13","298","2","298","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H26 N4 O5 Pt -","- C28 H26 N4 O5 Pt -","- C112 H104 N16 O20 Pt4 -","4","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.047","0.0401","","","0.0708","0.0731","","","","","","1.195","","","","has coordinates","291344","2024-04-24","01:03:03","" "7248521","12.4667","0.0005","13.3851","0.0007","18.9089","0.0006","93.304","0.003","98.761","0.003","104.327","0.004","3006.5","0.2","293","2","293","2","","","","","","","","5","P -1","-P 1","2","","","","- C63.25 H74 N6 O4 Pt2 -","- C63.25 H74 N6 O4 Pt2 -","- C126.5 H148 N12 O8 Pt4 -","2","1","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.1412","0.0672","","","0.0903","0.1135","","","","","","0.97","","","","has coordinates,has disorder","291344","2024-04-24","01:03:03","" "7248522","11.0129","0.0007","11.7585","0.0008","20.8975","0.0011","105.026","0.005","96.671","0.005","95.534","0.005","2573.2","0.3","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C27 H29 N3 O2 Pt -","- C27 H29 N3 O2 Pt -","- C108 H116 N12 O8 Pt4 -","4","2","","Thakur, Vasudha; Thomas, Jisha Mary; Adnan, Mohammad; Sivasankar, Chinnappan; Vijaya Prakash, G.; Thirupathi, Natesan","Syntheses, structural, photophysical and theoretical studies of heteroleptic cycloplatinated guanidinate(1−) complexes bearing acetylacetonate and picolinate ancillary ligands","RSC Advances","2024","14","19","13291","13305","10.1039/D4RA00828F","","","0.71073","MoKα","","0.1699","0.0761","","","0.0841","0.1056","","","","","","0.98","","","","has coordinates","291344","2024-04-24","01:03:03","" "7248537","10.1548","0.0004","13.1857","0.0005","17.8205","0.0007","90","","99.4068","0.0013","90","","2354.05","0.16","180","","180","","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","phenoxathiin derivative","","- C25 H33.87 O4 S -","- C25 H33.87 O4 S -","- C100 H135.48 O16 S4 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.5418","CuKα","","0.0374","0.0369","","0.1038","0.1032","0.1038","","","","","","1.0017","","","","has coordinates,has disorder","291362","2024-04-26","01:05:16","" "7248538","5.9326","0.0003","16.612","0.0009","26.1176","0.0014","90","","91.059","0.003","90","","2573.5","0.2","180","","180","","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","1,3,6,8-Tetra-tert-butyl-4-methoxydibenzofuran","","- C29 H42 O2 -","- C29 H42 O2 -","- C116 H168 O8 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.5418","CuKα","","0.0605","0.0525","","0.1486","0.1394","0.1486","","","","","","1","","","","has coordinates","291362","2024-04-26","01:05:17","" "7248539","11.7442","0.0004","14.1049","0.0005","15.542","0.0006","63.69","0.0012","70.5333","0.0014","73.0289","0.0013","2144.02","0.14","180","","180","","","","101","","","","","4","P -1","-P 1","2","","","","- C43 H54 O10 S3 -","- C43 H54 O10 S3 -","- C86 H108 O20 S6 -","2","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","0.71073","MoKα","","0.059","0.0507","","0.1597","0.1447","0.1597","","","","","","0.9601","","","","has coordinates","291362","2024-04-26","01:05:17","" "7248540","10.46238","0.00007","26.51526","0.00017","9.96612","0.00008","90","","101.307","0.0007","90","","2711.07","0.03","95","","95","","","","101","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C29 H42 O4 S -","- C29 H42 O4 S -","- C116 H168 O16 S4 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.54184","CuKα","","0.0333","0.0319","","0.0869","0.0854","0.0869","","","","","","0.9837","","","","has coordinates","291362","2024-04-26","01:05:17","" "7248541","11.9907","0.00012","11.76474","0.00011","21.924","0.0003","90","","102.934","0.0011","90","","3014.29","0.06","120","","120","","","","101","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C38 H36 O3 S -","- C38 H36 O3 S -","- C152 H144 O12 S4 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.54184","CuKα","","0.0348","0.0327","","0.0923","0.0898","0.0923","","","","","","0.9799","","","","has coordinates","291362","2024-04-26","01:05:17","" "7248542","15.7249","0.0004","14.5795","0.0004","18.6923","0.0005","90","","91.5925","0.0012","90","","4283.8","0.2","260","","260","","","","101","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C43 H54 O10 S3 -","- C43 H54 O10 S3 -","- C172 H216 O40 S12 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.54178","CuKα","","0.0495","0.0472","","0.1406","0.1357","0.1406","","","","","","0.9659","","","","has coordinates,has disorder","291362","2024-04-26","01:05:17","" "7248543","21.367","0.0013","9.5552","0.0006","25.775","0.0015","90","","100.165","0.003","90","","5179.8","0.5","180","","180","","","","101","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C48 H64 Cl2 O12 S4 -","- C48 H64 Cl2 O12 S4 -","- C192 H256 Cl8 O48 S16 -","4","1","","Mamleev, Kamil; Čejka, Jan; Eigner, Václav; Krupička, Martin; Dvořáková, Hana; Lhoták, Pavel","Reactivity of phenoxathiin-based thiacalixarenes towards C-nucleophiles","RSC Advances","2024","14","19","13463","13473","10.1039/D4RA02524E","","","1.5418","CuKα","","0.0945","0.0901","","0.2637","0.2577","0.2637","","","","","","0.9993","","","","has coordinates,has disorder","291362","2024-04-26","01:05:17","" "7248544","9.4024","0.0003","6.9264","0.0002","19.9477","0.0006","90","","100.097","0.001","90","","1278.97","0.07","297","2","297","2","","","","","","","","6","P 1 21/m 1","-P 2yb","11","","","","- C17 H17 I4 N5 O3 S -","- C17 H17 I4 N5 O3 S -","- C34 H34 I8 N10 O6 S2 -","2","0.5","","Mohammed Hashim, K. K.; Manoj, E.","Aminoguanidine-based bioactive proligand as AIEE probe for anticancer and anticovid studies","RSC Advances","2024","14","19","13654","13668","10.1039/D4RA00554F","","","0.71073","MoKα","","0.0569","0.0394","","","0.0819","0.0888","","","","","","1.107","","","","has coordinates","291363","2024-04-26","01:05:40","" "7248547","25.653","0.016","38.97","0.02","8.972","0.006","90","","90","","90","","8969","9","273","2","273","2","","","","","","","","6","F d d 2","F 2 -2d","43","","","","- C16 H23 Cl N2 O8 Zn2 -","- C16 H23 Cl N2 O8 Zn2 -","- C256 H368 Cl16 N32 O128 Zn32 -","16","1","","Middya, Puspendu; Frontera, Antonio; Chattopadhyay, Shouvik","The crucial role of hydrogen bonding in shaping the structures of zinc-based coordination polymers using tridentate N, N, O donor reduced Schiff base ligands and bridging acetates","RSC Advances","2024","14","20","13905","13914","10.1039/D4RA00550C","","","0.71073","MoKα","","0.0441","0.0378","","","0.1044","0.1158","","","","","","1.129","","","","has coordinates","291376","2024-04-27","01:07:51","" "7248548","14.662","0.008","16.055","0.009","21.525","0.013","90","","90","","90","","5067","5","293","2","293","2","","","","","","","","6","A e a 2","A 2 -2ab","41","","","","- C17 H24 Br2 N2 O7 Zn2 -","- C17 H24 Br2 N2 O7 Zn2 -","- C136 H192 Br16 N16 O56 Zn16 -","8","1","","Middya, Puspendu; Frontera, Antonio; Chattopadhyay, Shouvik","The crucial role of hydrogen bonding in shaping the structures of zinc-based coordination polymers using tridentate N, N, O donor reduced Schiff base ligands and bridging acetates","RSC Advances","2024","14","20","13905","13914","10.1039/D4RA00550C","","","0.71073","MoKα","","0.0476","0.0359","","","0.1029","0.1134","","","","","","0.959","","","","has coordinates","291376","2024-04-27","01:07:52","" "7248561","9.2975","0.0003","10.1675","0.0003","10.6317","0.0002","73.401","0.002","64.496","0.003","69.395","0.003","838.3","0.05","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C18 H23 N2 O3 -","- C18 H23 N2 O3 -","- C36 H46 N4 O6 -","2","1","","Rebbah, Bahija; El Haib, Abderrahim; Lahmady, Sara; Forsal, Issam; Gouygou, Maryse; Mallet-Ladeira, Sonia; Medaghri-Alaoui, Abdelouahid; Rakib, El Mostapha; Hannioui, Abdellah","Synthesis, characterization, and inhibition effects of a novel eugenol derivative bearing pyrrole functionalities on the corrosion of mild steel in a HCl acid solution.","RSC advances","2024","14","20","14152","14160","10.1039/d4ra01337a","","x-ray","1.54184","CuKα","","0.0433","0.0415","","","0.1077","0.1093","","","","","","1.024","","","","has coordinates,has disorder","291430","2024-05-01","01:06:36","" "7248578","14.3029","0.0005","24.787","0.0009","55.5667","0.0017","90","","95.516","0.001","90","","19608.6","1.2","100","2","100","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C205 H287 Dy3 F12 N4 O9 S4 -","- C205 H287 Dy3 F12 N4 O9 S4 -","- C820 H1148 Dy12 F48 N16 O36 S16 -","4","1","","Rogacz, Katarzyna; Magott, Michał; Baś, Sebastian; Foltyn, Magdalena; Rams, Michał; Pinkowicz, Dawid","A photochromic trinuclear dysprosium(iii) single-molecule magnet with two distinct relaxation processes","RSC Advances","2024","14","21","14515","14522","10.1039/D4RA01645A","","","0.71073","MoKα","","0.1542","0.0668","","","0.1274","0.1578","","","","","","0.993","","","","has coordinates,has disorder","291472","2024-05-03","01:08:47","" "7248596","26.628","0.003","6.9771","0.0007","14.7128","0.0015","90","","97.479","0.002","90","","2710.2","0.5","293","2","293","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C32 H28 Cu2 N4 O4 -","- C32 H28 Cu2 N4 O4 -","- C128 H112 Cu8 N16 O16 -","4","0.5","","Majumdar, Dhrubajyoti; Gassoumi, Bouzid; Dey, Arka; Roy, Sourav; Ayachi, Sahbi; Hazra, Suman; Dalai, Sudipta","Synthesis, characterization, crystal structure, and fabrication of photosensitive Schottky device of a binuclear Cu(ii)-Salen complex: a DFT investigations","RSC Advances","2024","14","21","14992","15007","10.1039/D4RA01846J","","","0.71073","MoKα","","0.0346","0.0307","","","0.0799","0.0822","","","","","","1.181","","","","has coordinates","291790","2024-05-09","01:18:41","" "7248605","5.6414","0.0002","32.4145","0.0013","6.7458","0.0003","90","","97.556","0.002","90","","1222.85","0.09","0","2","0","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C H2 Cl N4 O3 -","- C7.5 H3 Cl N O -","- C60 H24 Cl8 N8 O8 -","8","2","","Le, Phong Q.; Dinh, Van M.; Nguyen, Huong D. T.; Ha, Hiep Q.; Truong, Thanh V.","Iodine-promoted amide formation via oxidative cleavage of indoles: novel quinazoline-4(3H)-one and tryptanthrin syntheses","RSC Advances","2024","14","22","15597","15603","10.1039/D4RA01807A","","","0.71073","MoKα","","0.0695","0.0429","","","0.0798","0.0879","","","","","","1.051","","","","has coordinates","291854","2024-05-15","01:14:49","" "7248606","12.0685","0.0004","14.1345","0.0004","18.6642","0.0006","90","","95.688","0.002","90","","3168.1","0.17","","","0","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H13 Br N2 O -","- C20 H13 Br N2 O -","- C160 H104 Br8 N16 O8 -","8","2","","Le, Phong Q.; Dinh, Van M.; Nguyen, Huong D. T.; Ha, Hiep Q.; Truong, Thanh V.","Iodine-promoted amide formation via oxidative cleavage of indoles: novel quinazoline-4(3H)-one and tryptanthrin syntheses","RSC Advances","2024","14","22","15597","15603","10.1039/D4RA01807A","","","0.71073","MoKα","","0.0492","0.0306","","","0.0618","0.069","","","","","","1.0404","","","","has coordinates","292638","2024-06-28","09:33:37","" "7248607","8.87694","0.00013","11.7651","0.0002","22.7128","0.0003","90","","90","","90","","2372.08","0.06","100","0.1","100","0.1","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C28 H26 N2 O3 S -","- C28 H26 N2 O3 S -","- C112 H104 N8 O12 S4 -","4","1","","Liu, Tingting; Wang, Jianbin; Xiao, Rou; Zhao, Junling","Switchable divergent synthesis of chiral indole derivatives via catalytic asymmetric dearomatization of 2,3-disubstituted indoles","RSC Advances","2024","14","22","15591","15596","10.1039/D4RA03231D","","x-ray","1.54184","CuKα","","0.0395","0.0364","","","0.0995","0.1019","","","","","","1.067","","","","has coordinates","291855","2024-05-15","01:15:06","" "7248641","6.9862","0.0002","7.4451","0.0002","10.5854","0.0002","92.553","0.002","97.855","0.002","91.766","0.002","544.49","0.02","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C10 H10 B F O2 Si -","- C10 H10 B F O2 Si -","- C20 H20 B2 F2 O4 Si2 -","2","1","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","x-ray","0.71073","MoKα","","0.0304","0.0284","","","0.0768","0.0783","","","","","","1.046","","","","has coordinates","291948","2024-05-18","01:09:47","" "7248642","8.6127","0.0002","7.0177","0.0002","11.1617","0.0003","90","","97.153","0.002","90","","669.38","0.03","100","2","100","2","","","","","","","","7","P 1 21/m 1","-P 2yb","11","","6-Ethynyl-7-fluoro-1,1-dimethylbenzo[c][1,2,5]oxasilaborol-3(1H)-ol MeCN monosolvate","","- C12 H13 B F N O2 Si -","- C12 H13 B F N O2 Si -","- C24 H26 B2 F2 N2 O4 Si2 -","2","0.5","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","x-ray","0.71073","MoKα","","0.0402","0.0335","","","0.0916","0.0971","","","","","","1.085","","","","has coordinates","291948","2024-05-18","01:09:47","" "7248643","6.9876","0.0003","7.7137","0.0004","10.6833","0.0005","85.701","0.004","81.858","0.004","89.401","0.004","568.42","0.05","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","6-Ethynyl-7-chloro-1,1-dimethylbenzo[c][1,2,5]oxasilaborol-3(1H)-ol","","- C10 H10 B Cl O2 Si -","- C10 H10 B Cl O2 Si -","- C20 H20 B2 Cl2 O4 Si2 -","2","1","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","x-ray","1.54184","CuKα","","0.0302","0.03","","","0.0773","0.0775","","","","","","1.084","","","","has coordinates","291948","2024-05-18","01:09:48","" "7248644","8.8484","0.0004","11.1678","0.0004","12.0146","0.0005","89.089","0.003","77.254","0.003","80.69","0.003","1142.5","0.08","100","2","100","2","","","","","","","","9","P -1","-P 1","2","","7-Fluoro-1,1-dimethyl-6-(1-(2-fluorophenylsulfonyl)-1H-1,2,3-triazol-4-yl)benzo[c][1,2,5]oxasilaborol-3(1H)-ol","","- C17 H15 B Cl3 F2 N3 O4 S Si -","- C17 H15 B Cl3 F2 N3 O4 S Si -","- C34 H30 B2 Cl6 F4 N6 O8 S2 Si2 -","2","1","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","x-ray","0.71073","MoKα","","0.067","0.0489","","","0.1085","0.1181","","","","","","1.035","","","","has coordinates,has disorder","291948","2024-05-18","01:09:48","" "7248645","12.2547","0.0002","21.3124","0.0004","14.789","0.0002","90","","91.981","0.001","90","","3860.24","0.11","100","2","100","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C36 H40 F2 N8 O5 S2 Si2 -","- C36 H40 F2 N8 O5 S2 Si2 -","- C144 H160 F8 N32 O20 S8 Si8 -","4","1","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","x-ray","1.54178","CuKα","","0.0497","0.0445","","","0.117","0.1226","","","","","","1.017","","","","has coordinates","291948","2024-05-18","01:09:48","" "7248646","15.7378","0.0004","5.9671","0.0001","21.2618","0.0005","90","","97.318","0.002","90","","1980.41","0.08","100","2","100","2","","","","","","","","9","P 1 2/c 1","-P 2yc","13","","4-(7-Fluoro-3-hydroxy-1,1-dimethyl-1,3-dihydrobenzo[c][1,2,5]oxasilaborol-6-yl)-1H-1,2,3-triazol-3-ium 4-chlorophenylsulfonate","","- C16 H16 B Cl F N3 O5 S Si -","- C16 H16 B Cl F N3 O5 S Si -","- C64 H64 B4 Cl4 F4 N12 O20 S4 Si4 -","4","1","","Pacholak, P.; Durka, K.; Woźniak, K.; Krajewska, J.; Laudy, A. E.; Luliński, S.","Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition","RSC Advances","2024","14","23","16069","16082","10.1039/D4RA02137A","","","1.54178","CuKα","","0.036","0.0298","","","0.0764","0.081","","","","","","1.04","","","","has coordinates","291948","2024-05-18","01:09:48","" "7248669","14.6813","0.0005","15.2077","0.0005","16.935","0.0006","90","","110.478","0.001","90","","3542.1","0.2","170","2","170","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C38 H49 Cl N2 O2 Pd -","- C38 H49 Cl N2 O2 Pd -","- C152 H196 Cl4 N8 O8 Pd4 -","4","1","","Chen, Wei; Chen, Kai; Wang, Xuejie; Yang, Linjie; Chen, Wanzhi","Pd/NHC catalyzed reduction and coupling of nitroaromatics for the synthesis of diarylamines","RSC Advances","2024","14","24","16624","16628","10.1039/D4RA00921E","","","0.71073","MoKα","","0.032","0.0248","","","0.0558","0.0591","","","","","","1.044","","","","has coordinates","292000","2024-05-23","01:12:12","" "7248673","27.317","0.005","8.519","0.005","19.641","0.005","90","0.005","127.83","0.005","90","0.005","3610","2","293","2","293","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C21 H19 N3 O -","- C21 H19 N3 O -","- C168 H152 N24 O8 -","8","1","","Dunkel, Petra; Bogdán, Dóra; Deme, Ruth; Zimber, Ádám; Ballayová, Veronika; Csizmadia, Eszter; Kontra, Bence; Kalydi, Eszter; Bényei, Attila; Mátyus, Péter; Mucsi, Zoltán","C(sp3)–H cyclizations of 2-(2-vinyl)phenoxy-tert-anilines","RSC Advances","2024","14","24","16784","16800","10.1039/D3RA08974F","","","0.71069","MoKα","","0.1174","0.0726","","","","0.1909","","","","","","1.061","","","","has coordinates","292013","2024-05-24","01:09:28","" "7248674","8.745","0.001","9.836","0.001","17.535","0.001","90","","90","","90","","1508.3","0.2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C18 H15 N3 O -","- C18 H15 N3 O -","- C72 H60 N12 O4 -","4","1","","Dunkel, Petra; Bogdán, Dóra; Deme, Ruth; Zimber, Ádám; Ballayová, Veronika; Csizmadia, Eszter; Kontra, Bence; Kalydi, Eszter; Bényei, Attila; Mátyus, Péter; Mucsi, Zoltán","C(sp3)–H cyclizations of 2-(2-vinyl)phenoxy-tert-anilines","RSC Advances","2024","14","24","16784","16800","10.1039/D3RA08974F","","","0.71073","MoKα","","0.0694","0.0562","","","","0.1396","","","","","","1.095","","","","has coordinates","292013","2024-05-24","01:09:28","" "7248685","9.719","0.0005","9.719","0.0005","7.17","0.0006","90","","90","","120","","586.53","0.07","293","2","293","2","","","","","","","","6","P 63/m","-P 6c","176","apatite","Pb~5.09~Ca~3.78~K~1.13~(PO~4~)~6~F~0.87~","","- Ca3.78 F0.87 K1.13 O24 P6 Pb5.09 -","- Ca3.776 F0.866 K1.134 O24 P6 Pb5.0884 -","- Ca3.776 F0.866 K1.134 O24 P6 Pb5.0884 -","1","0.0833333","","Hamza, Mariam; Hamdi, Besma; Ben Ahmed, Ali; Capitelli, Francesco; El Feki, Hafed","Synthesis of a new potassium-substituted lead fluorapatite and its structural characterization","RSC Advances","2024","14","24","16876","16885","10.1039/D4RA01014K","","","0.71073","MoKα","","0.0575","0.0309","","","0.0546","0.0614","","","","","","0.971","","","","has coordinates","292029","2024-05-25","01:08:21","" "7248725","9.1249","0.0017","12.094","0.002","10.995","0.002","90","","108.971","0.011","90","","1147.5","0.4","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","Methyl 4-((3-(methoxycarbonyl)-2-methyl-1,1-dioxido-4-oxo-3,4-dihydro-2H-benzo[e][1,2]thiazin-3-yl)oxy)-2-methyl-2H-benzo[e][1,2]thiazine-3-carboxylate1,1-dioxide","","- C22 H20 N2 O10 S2 -","- C22 H20 N2 O10 S2 -","- C44 H40 N4 O20 S4 -","2","1","","Fatima, Muqudis; Siddiqui, Waseeq Ahmad; Choudhary, Muhammad Iqbal; Ashraf, Adnan; Niaz, Shanawer; Raza, Muhammad Asam; Alam, Seikh Mafiz; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Dahlous, Kholood Ahmed","Synthesis of dimeric 1,2-benzothiazine 1,1-dioxide scaffolds: molecular structures, Hirshfeld surface analysis, DFT and enzyme inhibition studies","RSC Advances","2024","14","24","16935","16944","10.1039/D4RA02009J","","","0.71073","MoKα","","0.0776","0.0546","","","0.1081","0.1212","","","","","","1.023","","","","has coordinates","292082","2024-05-29","01:59:30","" "7248726","8.4275","0.0007","12.5962","0.0012","17.3509","0.0016","71.203","0.005","87.757","0.004","77.684","0.005","1702.6","0.3","296","2","296","2","","","","","","","","6","P -1","-P 1","2","","Methyl 2-(3-chlorophenethyl)-4-((2-(3-chlorophenethyl)-3-(methoxycarbonyl)- 1,1-dioxido-4-oxo-3,4-dihydro-2H-benzo[e][1,2]thiazin-3-yl)oxy)-2H-benzo [e][1,2]thiazine-3-carboxylate 1,1-dioxide","","- C34 H26 Cl2 N2 O10 S2 -","- C34 H26 Cl2 N2 O10 S2 -","- C68 H52 Cl4 N4 O20 S4 -","2","1","","Fatima, Muqudis; Siddiqui, Waseeq Ahmad; Choudhary, Muhammad Iqbal; Ashraf, Adnan; Niaz, Shanawer; Raza, Muhammad Asam; Alam, Seikh Mafiz; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Dahlous, Kholood Ahmed","Synthesis of dimeric 1,2-benzothiazine 1,1-dioxide scaffolds: molecular structures, Hirshfeld surface analysis, DFT and enzyme inhibition studies","RSC Advances","2024","14","24","16935","16944","10.1039/D4RA02009J","","","0.71073","MoKα","","0.1016","0.0593","","","0.131","0.1511","","","","","","1.014","","","","has coordinates","292083","2024-05-29","01:59:47","" "7248727","8.112","0.004","17.079","0.01","22.56","0.013","90","","96.896","0.017","90","","3103","3","296","2","296","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","Methyl 4-((3-(methoxycarbonyl)-1,1-dioxido-4-oxo-2-phenethyl-3,4-dihydro- 2H-benzo[e][1,2]thiazin-3-yl)oxy)-2-phenethyl-2H-benzo[e][1,2]thiazine-3 -carboxylate 1,1-dioxide","","- C34 H28 N2 O10 S2 -","- C34 H28 N2 O10 S2 -","- C136 H112 N8 O40 S8 -","4","1","","Fatima, Muqudis; Siddiqui, Waseeq Ahmad; Choudhary, Muhammad Iqbal; Ashraf, Adnan; Niaz, Shanawer; Raza, Muhammad Asam; Alam, Seikh Mafiz; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Dahlous, Kholood Ahmed","Synthesis of dimeric 1,2-benzothiazine 1,1-dioxide scaffolds: molecular structures, Hirshfeld surface analysis, DFT and enzyme inhibition studies","RSC Advances","2024","14","24","16935","16944","10.1039/D4RA02009J","","","0.71073","MoKα","","0.192","0.0998","","","0.2014","0.2495","","","","","","1.01","","","","has coordinates","292084","2024-05-29","02:00:04","" "7248728","8.0501","0.0009","11.7489","0.0015","14.8904","0.0019","107.833","0.004","102.961","0.003","97.54","0.004","1275.8","0.3","296","2","296","2","","","","","","","","5","P -1","-P 1","2","","Methyl 2-ethyl-4-((2-ethyl-3-(methoxycarbonyl)-1,1-dioxido-4-oxo-3,4-dihydro- 2H-benzo[e][1,2]thiazin-3-yl)oxy)-2H-benzo[e][1,2]thiazine-3-carboxylate 1,1-dioxide","","- C24 H24 N2 O10 S2 -","- C24 H24 N2 O10 S2 -","- C48 H48 N4 O20 S4 -","2","1","","Fatima, Muqudis; Siddiqui, Waseeq Ahmad; Choudhary, Muhammad Iqbal; Ashraf, Adnan; Niaz, Shanawer; Raza, Muhammad Asam; Alam, Seikh Mafiz; Ashfaq, Muhammad; Tahir, Muhammad Nawaz; Dahlous, Kholood Ahmed","Synthesis of dimeric 1,2-benzothiazine 1,1-dioxide scaffolds: molecular structures, Hirshfeld surface analysis, DFT and enzyme inhibition studies","RSC Advances","2024","14","24","16935","16944","10.1039/D4RA02009J","","","0.71073","MoKα","","0.0702","0.0476","","","0.1187","0.1316","","","","","","1.044","","","","has coordinates","292085","2024-05-29","02:00:17","" "7248729","20.4271","0.0005","15.4067","0.0006","17.8809","0.0006","90","","90.371","0.002","90","","5627.3","0.3","170","0.1","170","0.1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C31 H21 N5 -","- C31 H21 N5 -","- C248 H168 N40 -","8","2","","Shi, Hai-Xiong; Bao, Hong-Wei; Wu, Gui-Yuan","Solvation controlled excited-state dynamics in a donor–acceptor phenazine-imidazole derivative","RSC Advances","2024","14","24","17071","17076","10.1039/D4RA02417F","","x-ray","1.54184","CuKα","","0.1161","0.0793","","","0.2063","0.2262","","","","","","1.04","","","","has coordinates","292086","2024-05-29","02:00:31","" "7248730","12.2945","0.0002","12.4454","0.0002","22.2997","0.0004","90","","90","","90","","3412.08","0.1","200","2","200","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","Gemmacolide X","","- C30 H38 Cl O14.5 -","- C30 H38 Cl O14.5 -","- C120 H152 Cl4 O58 -","4","1","","Do, Hai Nhat; Chen, Yu-Ta; Chien, Su-Ying; Chen, You-Ying; Zhang, Mingzi M.; Tsou, Lun Kelvin; Chen, Jih-Jung; Wen, Zhi-Hong; Lo, Yi-Hao; Zheng, Li-Guo; Sung, Ping-Jyun","Chlorine-containing polyacetoxybriarane diterpenoids from the octocoral Junceella fragilis","RSC Advances","2024","14","24","17195","17201","10.1039/D4RA03062A","","","1.54178","CuKα","","0.031","0.0292","","","0.0758","0.0772","","","","","","1.044","","","","has coordinates","292087","2024-05-29","02:00:56","" "7248731","22.8317","0.0003","22.8317","0.0003","10.2937","0.0002","90","","90","","120","","4647.06","0.12","200","2","200","2","","","","","","","","4","P 61","P 61","169","","Frajunolide I","","- C28 H35 Cl O12 -","- C28 H35 Cl O12 -","- C168 H210 Cl6 O72 -","6","1","","Do, Hai Nhat; Chen, Yu-Ta; Chien, Su-Ying; Chen, You-Ying; Zhang, Mingzi M.; Tsou, Lun Kelvin; Chen, Jih-Jung; Wen, Zhi-Hong; Lo, Yi-Hao; Zheng, Li-Guo; Sung, Ping-Jyun","Chlorine-containing polyacetoxybriarane diterpenoids from the octocoral Junceella fragilis","RSC Advances","2024","14","24","17195","17201","10.1039/D4RA03062A","","","1.54178","CuKα","","0.0393","0.0358","","","0.096","0.0989","","","","","","1.022","","","","has coordinates","292087","2024-05-29","02:00:58","" "7248732","17.0912","0.0003","5.88627","0.0001","13.7901","0.0003","90","","109.188","0.002","90","","1310.26","0.05","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H11 N O4 S -","- C15 H11 N O4 S -","- C60 H44 N4 O16 S4 -","4","1","","Lei, Xiaoqiang; Sun, Yanyan; Guo, Qinglan; Shi, Jiangong","Base mediated aza-[2 + 1] annulation and regioselective aziridine ring-opening cascade: mild synthesis of functionalized β-amino ketones from cyclic N-sulfonyl aldimines and α-carbonyl sulfonium salts","RSC Advances","2024","14","24","17178","17183","10.1039/D4RA02817A","","x-ray","1.54184","CuKα","","0.0416","0.0396","","","0.1085","0.1101","","","","","","1.069","","","","has coordinates","292088","2024-05-29","02:01:16","" "7248747","13.2488","0.0001","13.1966","0.0001","16.3122","0.0001","90","","93.179","0.001","90","","2847.62","0.04","150","0.1","150","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C37 H24 Cl2 N2 O2 -","- C37 H24 Cl2 N2 O2 -","- C148 H96 Cl8 N8 O8 -","4","1","","Chen‡, Meiling; Chen‡, Yuzhuo; Su, Zhongzhen; Li, Yuchun; Fei, Hanxiao; Zhang, Hua; Wu, Yunan","Achievement of efficient thermally activated delayed fluorescence materials based on 1,8-naphthalimide derivatives exhibiting piezochromic and thermochromic luminescence","RSC Advances","2024","14","25","17434","17439","10.1039/D4RA02981J","","x-ray","1.54184","CuKα","","0.0785","0.0757","","","0.2295","0.2324","","","","","","1.056","","","","has coordinates,has disorder","292112","2024-05-30","01:04:57","" "7248758","7.7207","0.0008","7.7941","0.0008","9.5977","0.0009","81.799","0.008","83.134","0.008","66.739","0.01","523.91","0.1","150.01","0.1","150.01","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C12 H24 Cl6 N4 O2 Pd -","- C12 H24 Cl6 N4 O2 Pd -","- C12 H24 Cl6 N4 O2 Pd -","1","0.5","","Bougossa, Sarra; Mhadhbi, Noureddine; Ben Ahmed, Ali; Hamdi, Mohamed; Elghniji, Kais; Erwann, Jeanneau; Hamden, Khaled; Oueslati, Abderrazek; Naïli, Houcine","Design of a new palladium(ii) halide complex as a bio-active material: synthesis, physico-chemical studies, DFT-computations and evaluation of anti-inflammatory, antioxidant and anti-gastric damage activities","RSC Advances","2024","14","25","17413","17433","10.1039/D4RA02984D","","x-ray","0.71073","MoKα","","0.078","0.0558","","","0.1286","0.1587","","","","","","1.191","","","","has coordinates","292125","2024-05-31","01:18:48","" "7248759","16.8509","0.0003","16.8509","0.0003","16.8509","0.0003","90","","90","","90","","4784.86","0.15","296","2","100","2","","","","","","","","5","I -4 3 m","I -4 2 3","217","","","","- C24 H30 N12 O4 Zn3 -","- C24 H30 N12 O4 Zn3 -","- C96 H120 N48 O16 Zn12 -","4","0.0833333","","Sun, Yihui; Zhang, Hui; Lv, Yan; An, Shengli; Wang, Ruifen","ZIF-8/g-C3N4 photocatalysts: enhancing CO2 reduction through improved adsorption and photocatalytic performance","RSC Advances","2024","14","25","17498","17506","10.1039/D4RA02548B","","","1.54178","CuKα","","0.0689","0.0688","","","0.2089","0.209","","","","","","2.098","","","","has coordinates","292126","2024-05-31","01:19:05","" "7248760","22.17","0.0004","7.54141","0.00012","34.4865","0.0004","90","","90","","90","","5765.9","0.15","293","2","293","2","","","","","","","","6","P b c n","-P 2n 2ab","60","","","","- C28 H25 Cl F2 N6 O4 -","- C28 H25 Cl F2 N6 O4 -","- C224 H200 Cl8 F16 N48 O32 -","8","1","","Patel, Upendra Kumar; Tiwari, Punit; Tilak, Ragini; Joshi, Gaurav; Kumar, Roshan; Agarwal, Alka","Synthesis of ciprofloxacin-linked 1,2,3-triazole conjugates as potent antibacterial agents using click chemistry: exploring their function as DNA gyrase inhibitors via in silico- and in vitro-based studies","RSC Advances","2024","14","24","17051","17070","10.1039/D4RA01332H","","","1.54184","CuKα","","0.065","0.0539","","","0.1532","0.1619","","","","","","1.063","","","","has coordinates","292127","2024-05-31","01:19:32","" "7248761","11.7334","0.0002","12.3293","0.0002","22.1027","0.0004","97.262","0.001","98.652","0.002","102.266","0.001","3047.14","0.09","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","(1-(3-chlorophenyl)-1H-1,2,3-triazol-4-yl)methyl 7-(4-benzoylpiperazin-1-yl)-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate","","- C33 H28 Cl F N6 O4 -","- C33 H28 Cl F N6 O4 -","- C132 H112 Cl4 F4 N24 O16 -","4","2","","Patel, Upendra Kumar; Tiwari, Punit; Tilak, Ragini; Joshi, Gaurav; Kumar, Roshan; Agarwal, Alka","Synthesis of ciprofloxacin-linked 1,2,3-triazole conjugates as potent antibacterial agents using click chemistry: exploring their function as DNA gyrase inhibitors via in silico- and in vitro-based studies","RSC Advances","2024","14","24","17051","17070","10.1039/D4RA01332H","","","1.54184","CuKα","","0.0866","0.0655","","","0.1963","0.2152","","","","","","1.069","","","","has coordinates","292127","2024-05-31","01:19:34","" "7248766","7.4408","0.0001","8.1893","0.0002","12.2524","0.0003","87.694","0.002","82.047","0.002","85.253","0.002","736.57","0.03","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","tricarbonyl-imidazole-(quinolin-8-olato-N,O)-rhenium(I)","","- C15 H10 N3 O4 Re -","- C15 H10 N3 O4 Re -","- C30 H20 N6 O8 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","0.71073","MoKα","","0.0189","0.0166","","","0.0317","0.0324","","","","","","1.077","","","","has coordinates","292224","2024-06-06","01:21:04","" "7248767","10.2609","0.0001","17.445","0.0002","23.0438","0.0003","90","","93.555","0.001","90","","4116.94","0.08","100","0.1","100","0.1","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C22 H15.5 N3.5 O4 Re -","- C22 H15.5 N3.5 O4 Re -","- C176 H124 N28 O32 Re8 -","8","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0294","0.0251","","","0.06","0.0626","","","","","","1.037","","","","has coordinates,has disorder","292224","2024-06-06","01:21:05","" "7248768","8.1183","0.0002","20.2662","0.0004","10.2281","0.0002","90","","95.549","0.002","90","","1674.91","0.06","100","0.1","100","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","tricarbonyl-(3,5-dimethylpyrazole)-(quinolin-8-olato-N,O)-rhenium(I)","","- C17 H14 N3 O4 Re -","- C17 H14 N3 O4 Re -","- C68 H56 N12 O16 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","x-ray","0.71073","MoKα","","0.0332","0.0258","","","0.0488","0.052","","","","","","1.083","","","","has coordinates","292224","2024-06-06","01:21:06","" "7248769","13.0393","0.0001","9.4738","0.0001","14.1877","0.0001","90","","115.34","0.001","90","","1584","0.03","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","tricarbonyl-(2-methylimidazole)-(quinolin-8-olato-N,O)-rhenium(I)","","- C16 H12 N3 O4 Re -","- C16 H12 N3 O4 Re -","- C64 H48 N12 O16 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0212","0.0182","","","0.0424","0.0441","","","","","","1.047","","","","has coordinates","292224","2024-06-06","01:21:06","" "7248770","7.37137","0.00015","8.22667","0.00018","12.8439","0.0004","104.939","0.002","94.72","0.002","93.3929","0.0017","747.38","0.03","100.01","0.1","100.01","0.1","","","","","","","","5","P -1","-P 1","2","","tricarbonyl-imidazole-(2-methylquinolin-8-olato-N,O)-rhenium(I)","","- C16 H12 N3 O4 Re -","- C16 H12 N3 O4 Re -","- C32 H24 N6 O8 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","x-ray","1.54184","CuKα","","0.0167","0.0159","","","0.0389","0.0394","","","","","","1.051","","","","has coordinates","292224","2024-06-06","01:21:06","" "7248771","7.5357","0.0003","8.1793","0.0003","12.8369","0.0006","85.268","0.003","78.455","0.004","84.5","0.003","770.02","0.06","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","tricarbonyl-imidazole-(5-chloroquinolin-8-olato-N,O)-rhenium(I)","","- C15 H9 Cl N3 O4 Re -","- C15 H9 Cl N3 O4 Re -","- C30 H18 Cl2 N6 O8 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","0.71073","MoKα","","0.0202","0.0182","","","0.041","0.0418","","","","","","1.044","","","","has coordinates","292224","2024-06-06","01:21:06","" "7248772","11.5721","0.0003","15.9025","0.0005","9.6875","0.0003","90","","106.476","0.003","90","","1709.54","0.09","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","tricarbonyl-(3,5-dimethylpyrazole)-(2-methylquinolin-8-olato-N,O)-rhenium(I)","","- C18 H16 N3 O4 Re -","- C18 H16 N3 O4 Re -","- C72 H64 N12 O16 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","0.71073","MoKα","","0.0215","0.0177","","","0.0371","0.0386","","","","","","1.087","","","","has coordinates","292224","2024-06-06","01:21:07","" "7248773","8.1187","0.0002","9.2533","0.0003","11.835","0.0004","92.174","0.003","102.111","0.003","92.651","0.002","867.35","0.05","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","tricarbonyl-imidazole-(quinolin-8-olato-N,O)-rhenium(I) methanol solvate","","- C16 H14 N3 O5 Re -","- C16 H14 N3 O5 Re -","- C32 H28 N6 O10 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","0.71073","MoKα","","0.0274","0.0247","","","0.045","0.0463","","","","","","1.013","","","","has coordinates","292224","2024-06-06","01:21:07","" "7248774","6.45743","0.00012","15.9593","0.0003","15.6659","0.0002","90","","100.521","0.0016","90","","1587.32","0.05","100","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","methanol-tricarbonyl-(5-chloroquinolin-8-olato-N,O)-rhenium(I) methanol solvate","","- C14 H13 Cl N O6 Re -","- C14 H13 Cl N O6 Re -","- C56 H52 Cl4 N4 O24 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0254","0.0192","","","0.0427","0.0442","","","","","","1.032","","","","has coordinates","292224","2024-06-06","01:21:07","" "7248775","7.4449","0.0002","9.4022","0.0004","16.3685","0.0007","74.151","0.004","77.427","0.003","72.802","0.003","1041.18","0.07","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","tricarbonyl-(5-phenyl-1H-pyrazole)-(5-chloroquinolin-8-olato-N,O)-rhenium(I) methanol solvate","","- C22 H18 N3 O5 Re -","- C22 H18 N3 O5 Re -","- C44 H36 N6 O10 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0253","0.0246","","","0.0637","0.0641","","","","","","1.104","","","","has coordinates","292224","2024-06-06","01:21:09","" "7248776","7.96094","0.00006","19.9948","0.0002","11.1475","0.00011","90","","95.6676","0.0008","90","","1765.76","0.03","100.01","0.1","100.01","0.1","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","tricarbonyl-(3,5-dimethylpyrazole)-(5-chloroquinolin-8-olato-N,O)-rhenium(I)","","- C17 H13 Cl N3 O4 Re -","- C17 H13 Cl N3 O4 Re -","- C68 H52 Cl4 N12 O16 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","x-ray","1.54184","CuKα","","0.0253","0.0217","","","0.0431","0.0444","","","","","","1.054","","","","has coordinates","292224","2024-06-06","01:21:18","" "7248777","7.895","0.0002","10.3914","0.0004","12.3893","0.0003","79.872","0.003","84.527","0.002","83.437","0.003","991.07","0.05","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","tricarbonyl-(5-phenyl-1H-pyrazole)-(2-methylquinolin-8-olato-N,O)-rhenium(I)","","- C22 H16 N3 O4 Re -","- C22 H16 N3 O4 Re -","- C44 H32 N6 O8 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0224","0.0218","","","0.0549","0.0552","","","","","","1.087","","","","has coordinates","292224","2024-06-06","01:21:21","" "7248778","9.8714","0.0006","10.2322","0.0006","11.4613","0.0006","67.014","0.005","75.785","0.005","65.454","0.006","964.62","0.11","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","tricarbonyl-(5-phenyl-1H-pyrazole)-(5-chloroquinolin-8-olato-N,O)-rhenium(I)","","- C21 H13 Cl N3 O4 Re -","- C21 H13 Cl N3 O4 Re -","- C42 H26 Cl2 N6 O8 Re2 -","2","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0365","0.0289","","","0.0635","0.0659","","","","","","1.035","","","","has coordinates","292224","2024-06-06","01:21:30","" "7248779","14.2506","0.0003","15.7017","0.0003","18.1171","0.0004","90","","111.31","0.003","90","","3776.69","0.16","100","0.1","100","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","tricarbonyl-(2-methylimidazole)-(5-chloroquinolin-8-olato-N,O)-rhenium(I)acetonitrile solvate","","- C18 H14 Cl N4 O4 Re -","- C18 H14 Cl N4 O4 Re -","- C144 H112 Cl8 N32 O32 Re8 -","8","2","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0336","0.0276","","","0.068","0.0714","","","","","","1.035","","","","has coordinates,has disorder","292224","2024-06-06","01:21:32","" "7248780","7.23554","0.00004","17.95049","0.00011","12.33498","0.0001","90","","93.2445","0.0006","90","","1599.52","0.019","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","tricarbonyl-(2-methylimidazole)-(2-methylquinolin-8-olato-N,O)-rhenium(I)","","- C17 H14 N3 O4 Re -","- C17 H14 N3 O4 Re -","- C68 H56 N12 O16 Re4 -","4","1","","Łyczko, Krzysztof; Pogorzelska, Anna; Częścik, Urszula; Koronkiewicz, Mirosława; Rode, Joanna E.; Bednarek, Elżbieta; Kawęcki, Robert; Węgrzyńska, Karolina; Baraniak, Anna; Milczarek, Małgorzata; Dobrowolski, Jan Cz.","Tricarbonyl rhenium(i) complexes with 8-hydroxyquinolines: structural, chemical, antibacterial, and anticancer characteristics","RSC Advances","2024","14","25","18080","18092","10.1039/D4RA03141E","","","1.54184","CuKα","","0.0134","0.0126","","","0.03","0.0303","","","","","","1.064","","","","has coordinates","292224","2024-06-06","01:21:40","" "7248849","11.9361","0.00009","16.71476","0.00012","20.98996","0.00014","90","","90","","90","","4187.69","0.05","100","0.1","100","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","6'-(Diethylamino)-1',2'-benzofluoran","9-(diethylamino)spiro[12H-benzo[a]xanthene-12,1'(3'H)-isobenzofuran]-3'-one","","- C28 H23 N O3 -","- C28 H23 N O3 -","- C224 H184 N8 O24 -","8","1","","Pawłów, J; Wilk-Kozubek, M; Czajkowski, M.; Zdończyk, M; Cybińska, J","Innovative use of liquid crystalline acids as color developers in leuco dye-based temperature sensors.","RSC advances","2024","14","26","18663","18670","10.1039/d4ra01867b","","","1.54184","CuKα","","0.0348","0.0346","","","0.0844","0.0846","","","","","","1.041","","","","has coordinates","292340","2024-06-13","01:30:07","" "7248850","13.485","0.0018","11.0322","0.0014","21.808","0.003","90","","104.878","0.004","90","","3135.6","0.7","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C40 H31 N3 O3 -","- C40 H31 N3 O3 -","- C160 H124 N12 O12 -","4","1","","Arumugam, Natarajan; Darshan V. M., Datta; Venketesh, Vishal; Pradhan, Sai Sanwid; Garg, Anuj; Sivaramakrishnan, Venketesh; Kanchi, Subbarao; Mahalingam, Sakkarapalayam M.","Synthesis, computational docking and molecular dynamics studies of a new class of spiroquinoxalinopyrrolidine embedded chromanone hybrids as potent anti-cholinesterase agents","RSC Advances","2024","14","26","18815","18831","10.1039/D4RA02432J","","","0.71073","MoKα","","0.1739","0.0909","","","0.164","0.1948","","","","","","1.129","","","","has coordinates","292341","2024-06-13","01:30:35","" "7248851","10.2438","0.0001","19.806","0.0002","35.2267","0.0003","90","","94.35","0.001","90","","7126.51","0.12","119.99","0.1","119.99","0.1","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","EKR126","","- C53 H42 Cr N O12 S32 -","- C53 H42 Cr N O12 S32 -","- C212 H168 Cr4 N4 O48 S128 -","4","0.5","","Blundell, Toby J.; Ogar, Joseph O.; Brannan, Michael J.; Rusbridge, Elizabeth K.; Wallis, John D.; Akutsu, Hiroki; Nakazawa, Yasuhiro; Imajo, Shusaku; Martin, Lee","BEDT-TTF radical-cation salts with tris(oxalato)chromate and guest additives.","RSC advances","2024","14","26","18444","18452","10.1039/d4ra03425b","","x-ray","1.54184","CuKα","","0.0885","0.0877","","","0.1834","0.1838","","","","","","1.204","","","","has coordinates,has disorder","292342","2024-06-13","01:31:05","" "7248852","10.327","0.0002","19.9211","0.0004","35.3072","0.0007","90","","93.139","0.007","90","","7252.7","0.3","298","","298.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C52 H40 Cr O14 S32 -","- C52 H40 Cr O14 S32 -","- C208 H160 Cr4 O56 S128 -","4","0.5","","Blundell, Toby J.; Ogar, Joseph O.; Brannan, Michael J.; Rusbridge, Elizabeth K.; Wallis, John D.; Akutsu, Hiroki; Nakazawa, Yasuhiro; Imajo, Shusaku; Martin, Lee","BEDT-TTF radical-cation salts with tris(oxalato)chromate and guest additives.","RSC advances","2024","14","26","18444","18452","10.1039/d4ra03425b","","","0.71075","MoKα","","0.0457","0.0391","","","0.105","0.1097","","","","","","1.04","","","","has coordinates,has disorder","292342","2024-06-13","01:31:06","" "7248853","10.3201","0.0011","19.97","0.003","35.467","0.004","90","","92.995","0.007","90","","7299.5","1.6","298","","298","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C53 H39 Cr O15 S32 -","- C46 H35 Cr O13 S32 -","- C184 H140 Cr4 O52 S128 -","4","0.5","","Blundell, Toby J.; Ogar, Joseph O.; Brannan, Michael J.; Rusbridge, Elizabeth K.; Wallis, John D.; Akutsu, Hiroki; Nakazawa, Yasuhiro; Imajo, Shusaku; Martin, Lee","BEDT-TTF radical-cation salts with tris(oxalato)chromate and guest additives.","RSC advances","2024","14","26","18444","18452","10.1039/d4ra03425b","","","0.71075","MoKα","","0.2843","0.2301","","","0.5352","0.5535","","","","","","3.33","","","","has coordinates","292342","2024-06-13","01:31:06","" "7248854","6.5405","0.0004","10.9927","0.0006","14.465","0.0008","68.977","0.002","81.458","0.002","76.809","0.002","942.61","0.09","200","","200","","","","","","","","","6","P -1","-P 1","2","","Pr(hpo)(mpo)2(H2O)2","","- C15 H16 N3 O6 Pr S2 -","- C15 H16 N3 O6 Pr S2 -","- C30 H32 N6 O12 Pr2 S4 -","2","1","","Zhu, Qiuyin; Hsu, Wayne; Wang, Shenglong; Lin, Fenglong; Wu, Yincai; Fang, Yimin; Chen, Jinglin; Song, Lijun","Synthesis, antimicrobial activity and application of polymers of praseodymium complexes based on pyridine nitrogen oxide.","RSC advances","2024","14","26","18519","18527","10.1039/d4ra03003f","","","0.71073","MoKα","","0.0387","0.0305","","","0.0665","0.0724","","","","","","1.097","","","","has coordinates","292343","2024-06-13","01:31:37","" "7248855","8.4728","0.0005","9.7873","0.0005","13.7277","0.0008","92.265","0.002","107.891","0.002","92.928","0.002","1080.09","0.11","200","2","200","","","","","","","","","6","P -1","-P 1","2","","Pr2(mpo)6(H2O)2","","- C30 H40 N6 O14 Pr2 S6 -","- C30 H40 N6 O14 Pr2 S6 -","- C30 H40 N6 O14 Pr2 S6 -","1","0.5","","Zhu, Qiuyin; Hsu, Wayne; Wang, Shenglong; Lin, Fenglong; Wu, Yincai; Fang, Yimin; Chen, Jinglin; Song, Lijun","Synthesis, antimicrobial activity and application of polymers of praseodymium complexes based on pyridine nitrogen oxide.","RSC advances","2024","14","26","18519","18527","10.1039/d4ra03003f","","","0.71073","MoKα","","0.0371","0.0371","","","0.0941","0.0942","","","","","","1.077","","","","has coordinates","292343","2024-06-13","01:31:37","" "7248856","11.3667","0.0003","7.8133","0.0002","14.3984","0.0004","90","","105.313","0.001","90","","1233.34","0.06","293","2","293","2","","","","","","","","6","P 1 21 1","P 2yb","4","","","","- C27 H22 Br F3 N2 O3 -","- C27 H24 Br F3 N2 O3 -","- C54 H48 Br2 F6 N4 O6 -","2","1","","Pu, Yiru; Wang, Maolin; Tian, Wanrong; Ge, Xian; Zhu, Dikai; Wang, Chuanqi; Zeng, Yingjie; Tao, Feiyan; Deng, Yun; Lu, Jun","N-heterocyclic carbene catalyzed [2 + 3] annulation reaction for the synthesis of trifluoroethyl 3,2'-spirooxindole γ-lactam.","RSC advances","2024","14","26","18453","18458","10.1039/d4ra02252a","","","1.54178","CuKα","","0.0367","0.0346","","","0.1131","0.1171","","","","","","0.982","","","","has coordinates","292344","2024-06-13","01:31:54","" "7248857","10.2357","0.0004","12.1215","0.0005","14.9718","0.0006","76.079","0.002","80.501","0.002","79.118","0.002","1756.6","0.12","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","Polymeric Cu-complex","","- C58 H88 Cu3 I2 N16 O10 -","- C58 H88 Cu3 I2 N16 O10 -","- C58 H88 Cu3 I2 N16 O10 -","1","0.5","","Bhuyan, Amar Jyoti; Nath, Partha Pratim; Bharali, Sourav Jyoti; Saikia, Lakhinath","A novel μ3-CO3 bridged linear polymeric Cu-complex ([Cu3(DMAP)83-CO3)2]I2) n ·xH2O: synthesis, characterization and catalytic applications in the synthesis of phenoxypyrimidines and arylthiopyrimidines via C-O and C-S cross-coupling reactions.","RSC advances","2024","14","26","18478","18488","10.1039/d4ra00001c","","","0.71073","MoKα","","0.0731","0.0453","","","0.111","0.1251","","","","","","1.009","","","","has coordinates","292345","2024-06-13","01:32:08","" "7248858","8.8506","0.0005","9.2538","0.0005","14.0175","0.0008","74.262","0.005","72.168","0.005","88.125","0.004","1050.34","0.11","170","","170","","","","","","","","","5","P -1","-P 1","2","","","","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","1.54184","CuKα","","0.0844","0.0829","","","0.2175","0.2197","","","","","","1.128","","","","has coordinates","292382","2024-06-14","01:08:32","" "7248859","10.067","0.0006","10.0808","0.0006","11.2764","0.0007","90.46","0.005","92.74","0.005","108.443","0.005","1084.03","0.12","150","2","150","2","","","","","","","","5","P -1","-P 1","2","","(u6-oxo)-tetradecakis(u2-oxo)-octaoxo-bis(N-(2-oxy-3-(methoxy)benzylidene)nicotinylhydrazonato)-octa-molybdenum","","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","0.71073","MoKα","","0.1312","0.0598","","","0.0615","0.0737","","","","","","0.934","","","","has coordinates","292382","2024-06-14","01:08:33","" "7248860","10.0231","0.0001","10.7273","0.0003","12.9277","0.0003","73.422","0.002","72.752","0.002","66.204","0.002","1192.6","0.05","169.99","0.1","169.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C32 H30 Mo8 N8 O29 -","- C32 H30 Mo8 N8 O29 -","- C32 H30 Mo8 N8 O29 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","1.54184","CuKα","","0.0386","0.036","","","0.0942","0.0968","","","","","","1.047","","","","has coordinates","292382","2024-06-14","01:08:33","" "7248861","8.9721","0.0003","10.7368","0.0002","16.4964","0.0004","104.858","0.002","104.62","0.002","94.02","0.002","1470.73","0.07","169.99","","169.99","","","","","","","","","5","P -1","-P 1","2","","[N'-(2-oxo-3-methoxybenzylidene)nicotinoylhydrazonium](acetone)dioxomolybdenum(vi) hexamolybdate acetone solvate","","- C40 H48 Mo8 N6 O33 -","- C40 H48 Mo8 N6 O33 -","- C40 H48 Mo8 N6 O33 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","1.54184","CuKα","","0.0477","0.0453","","","0.1229","0.1252","","","","","","1.069","","","","has coordinates,has disorder","292382","2024-06-14","01:08:33","" "7248862","10.1475","0.0004","10.3331","0.0005","14.6331","0.0005","108.527","0.004","92.219","0.003","110.565","0.004","1342.45","0.11","150","2","150","","","","","","","","","5","P -1","-P 1","2","","bis((aquo)-dioxo-(N-(2-oxy-3-methoxybenzylidene)nicotinylhydrazonato)-molybdenum(vi)) hexamolybdate acetone solvate","","- C34 H40 Mo8 N6 O33 -","- C34 H40 Mo8 N6 O33 -","- C34 H40 Mo8 N6 O33 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","","0.71073","MoKα","","0.1054","0.0517","","","0.0789","0.0898","","","","","","0.962","","","","has coordinates","292382","2024-06-14","01:08:34","" "7248863","10.6083","0.0008","10.7813","0.0006","12.8485","0.0006","106.66","0.005","106.352","0.006","99.224","0.005","1303.62","0.16","169.99","0.1","169.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C34 H40 Mo8 N6 O33 -","- C34 H40 Mo8 N6 O33 -","- C34 H40 Mo8 N6 O33 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","1.54184","CuKα","","0.0673","0.0634","","","0.1747","0.182","","","","","","1.05","","","","has coordinates","292382","2024-06-14","01:08:34","" "7248864","8.8403","0.0002","9.1695","0.0002","14.0494","0.0003","106.381","0.002","105.966","0.002","93.753","0.002","1037.78","0.04","169.99","0.1","169.99","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","- C28 H24 Mo8 N6 O29 -","1","0.5","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","x-ray","1.54184","CuKα","","0.0818","0.0802","","","0.1975","0.2002","","","","","","1.172","","","","has coordinates","292382","2024-06-14","01:08:34","" "7248865","11.2569","0.0003","9.2706","0.0002","21.2974","0.0005","90","","103.717","0.002","90","","2159.17","0.09","150","2","150","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","bis((aquo)-dioxo-(N-(2-oxy-3-methoxybenzylidene)nicotinylhydrazonato)-molybdenum(vi)) hexamolybdate","","- C56 H56 Mo16 N12 O62 -","- C56 H56 Mo16 N12 O62 -","- C56 H56 Mo16 N12 O62 -","1","0.25","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","","0.71073","MoKα","","0.05","0.0347","","","0.0709","0.0793","","","","","","1.06","","","","has coordinates","292382","2024-06-14","01:08:34","" "7248866","10.8391","0.0001","17.0475","0.0001","18.7075","0.0001","88.584","0.001","84.114","0.001","88.515","0.001","3436.54","0.04","170.15","","170.15","","","","","","","","","5","P -1","-P 1","2","","[(?2-oxo)[4-methoxy-2-oxidophenyl)methylidene]pyridin-1-ium-4-carbohydrazone-O,O',N)oxomolybdenum(VI)] {bis-[(?2-oxo)((4-methoxy-2-oxidophenyl)methylidene)pyridin-1-ium-4-carbohydrazidato-O,O',N)oxomolybdenum(VI)] dodecakis(?-oxido)-tetradecaoxooctamolybdenum(VI)}","","- C46 H42 Mo11 N11 O42 -","- C46 H42 Mo11 N11 O42 -","- C92 H84 Mo22 N22 O84 -","2","1","","Pisk, Jana; Vrdoljak, Višnja; Mandarić, Mirna; Hrenar, Tomica; Agustin, Dominique; Rubčić, Mirta","Impact of POM's coordination mode and Mo-hybrid constituents on the binding, stability, and catalytic properties of hybrid (pre)catalysts","RSC Advances","2024","14","27","19029","19040","10.1039/D4RA03563A","","","1.54184","CuKα","","0.0436","0.0389","","","0.1029","0.1058","","","","","","1.082","","","","has coordinates,has disorder","292382","2024-06-14","01:08:34","" "7248885","13.7061","0.0005","35.5623","0.0012","9.8813","0.0003","90","","106.416","0.004","90","","4620","0.3","180","0.1","180","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C42 H63 F6 N8 O4 P -","- C42 H63 F6 N8 O4 P -","- C168 H252 F24 N32 O16 P4 -","4","1","","Munteanu, Tatiana; Longevial, Jean-François; Canard, Gabriel; Jacquemin, Denis; Pascal, Simon; Siri, Olivier","Post-functionalization of triamino-phenazinium dyes to reach near-infrared emission","RSC Advances","2024","14","27","19257","19263","10.1039/D4RA03245D","","x-ray","1.54184","CuKα","","0.1501","0.1313","","","0.2814","0.2901","","","","","","1.124","","","","has coordinates,has disorder","292438","2024-06-18","01:17:10","" "7248887","6.9643","0.0008","17.995","0.002","11.248","0.0013","90","","104.494","0.004","90","","1364.8","0.3","300","2","300","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C18 H11 F O3 -","- C18 H11 F O3 -","- C72 H44 F4 O12 -","4","1","","Wang, Hua; Ma, Qin; Xu, Yifei; Sun, Yanyan; Zhao, Siyuan; Wang, Shaoyin; He, Xinwei","Modular access to furo[3,2-c]chromen-4-ones via Yb(OTf)3-catalyzed [3 + 2] annulation of 4-hydroxycoumarins with β-nitroalkenes","RSC Advances","2024","14","27","19581","19585","10.1039/D4RA03962A","","","0.71073","MoKα","","0.0886","0.0607","","","0.2102","0.2349","","","","","","1.089","","","","has coordinates","292457","2024-06-19","01:18:38","" "7248897","15.974","0.003","15.974","0.003","27.244","0.007","90","","90","","90","","6952","3","150","","150","","","","","","","","","5","P 4/m n c","-P 4 2n","128","","","","- C56 H49.5 N16 O18.24 Re5 -","- C56 H49.5 N16 O18.244 Re5 -","- C224 H198 N64 O72.976 Re20 -","4","0.25","","Shtemenko, Nataliia; Galiana-Rosello, Cristina; Gil-Martínez, Ariadna; Blasco, Salvador; Gonzalez-García, Jorge; Velichko, Helen; Holichenko, Oleksandr; Shtemenko, Olexandr; García-España, Enrique","Two rhenium compounds with benzimidazole ligands: synthesis and DNA interactions","RSC Advances","2024","14","28","19787","19793","10.1039/D4RA02669A","","","0.71073","MoKα","","0.0681","0.0584","","","0.1556","0.1637","","","","","","1.155","","","","has coordinates,has disorder","292496","2024-06-21","01:14:25","" "7248910","8.9077","0.0001","9.1847","0.0001","18.1367","0.0002","90","","93.364","0.001","90","","1481.29","0.03","133","2","133","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","5-phenyl-2-(phenylamino)-6H-1,3,4-thiadiazin-3-ium","","- C15 H14 Br N3 S -","- C15 H14 Br N3 S -","- C60 H56 Br4 N12 S4 -","4","1","","Tawfeek, Hendawy N.; Abdelmoez, Alshaimaa; Dahlous, Kholood A.; Youssif, Bahaa G. M.; Bräse, Stefan; Rissanen, Kari; Nieger, Martin; El-Sheref, Essmat M.","Convenient synthesis and X-ray determination of 2-amino-6H-1,3,4-thiadiazin-3-ium bromides endowed with antiproliferative activity","RSC Advances","2024","14","25","17866","17876","10.1039/D4RA02531H","","x-ray","1.54184","CuKα","","0.0203","0.0202","","","0.0512","0.0513","","","","","","1.089","","","","has coordinates","292632","2024-06-28","01:07:53","" "7248911","7.4414","0.0003","18.2272","0.0007","19.6573","0.0007","90","","90","","90","","2666.24","0.18","173","2","173","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","(Z)-N-(5-phenyl-3,6-dihydro-2H-1,3,4-thiadiazin-2-ylidene)prop-2-en-1-aminium bromide","","- C12 H14 Br N3 S -","- C12 H14 Br N3 S -","- C96 H112 Br8 N24 S8 -","8","1","","Tawfeek, Hendawy N.; Abdelmoez, Alshaimaa; Dahlous, Kholood A.; Youssif, Bahaa G. M.; Bräse, Stefan; Rissanen, Kari; Nieger, Martin; El-Sheref, Essmat M.","Convenient synthesis and X-ray determination of 2-amino-6H-1,3,4-thiadiazin-3-ium bromides endowed with antiproliferative activity","RSC Advances","2024","14","25","17866","17876","10.1039/D4RA02531H","","","1.54178","CuKα","","0.023","0.0223","","","0.0559","0.0563","","","","","","1.05","","","","has coordinates","292632","2024-06-28","01:07:55","" "7248912","10.3567","0.0008","12.1184","0.0009","22.4299","0.0015","91.283","0.006","95.977","0.007","110.754","0.008","2612.8","0.4","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C53 H66 Br4 O10 -","- C53 H66 Br4 O10 -","- C106 H132 Br8 O20 -","2","1","","Vinodh, Mickey; Alshammari, Anwar A.; Al-Azemi, Talal F.","Influence of halogen–halogen interactions in the self-assembly of pillar[5]arene-based supramolecular polymers","RSC Advances","2024","14","29","20553","20560","10.1039/D4RA03769C","","","0.71075","MoKα","","0.1513","0.0653","","","0.1549","0.179","","","","","","0.905","","","","has coordinates","292654","2024-06-29","01:12:18","" "7248913","10.2873","0.0003","12.1713","0.0004","22.771","0.0008","90.681","0.002","98.012","0.002","109.405","0.002","2657.77","0.15","296","2","296","2","","","","","","","","4","P -1","-P 1","2","","","","- C53 H66 Cl4 O10 -","- C53 H66 Cl4 O10 -","- C106 H132 Cl8 O20 -","2","1","","Vinodh, Mickey; Alshammari, Anwar A.; Al-Azemi, Talal F.","Influence of halogen–halogen interactions in the self-assembly of pillar[5]arene-based supramolecular polymers","RSC Advances","2024","14","29","20553","20560","10.1039/D4RA03769C","","","1.54178","CuKα","","0.0896","0.0717","","","0.2062","0.2235","","","","","","1.017","","","","has coordinates,has disorder","292654","2024-06-29","01:12:19","" "7248914","15.0762","0.0013","15.0762","0.0013","39.5384","0.0015","90","","90","","90","","8986.8","1.1","150","2","150","2","","","","","","","","4","I 41/a :2","-I 4ad","88","","","","- C49 H58 F2 O10 -","- C49 H58 F2 O10 -","- C392 H464 F16 O80 -","8","0.5","","Vinodh, Mickey; Alshammari, Anwar A.; Al-Azemi, Talal F.","Influence of halogen–halogen interactions in the self-assembly of pillar[5]arene-based supramolecular polymers","RSC Advances","2024","14","29","20553","20560","10.1039/D4RA03769C","","","0.71075","MoKα","","0.1069","0.0695","","","0.2023","0.2264","","","","","","1.041","","","","has coordinates","292654","2024-06-29","01:12:19","" "7248915","10.628","0.0009","12.2335","0.0012","23.534","0.002","88.021","0.006","77.859","0.006","71.497","0.005","2835","0.5","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","","","- C104 H128 I7 O20 -","- C104 H128 I7 O20 -","- C104 H128 I7 O20 -","1","0.5","","Vinodh, Mickey; Alshammari, Anwar A.; Al-Azemi, Talal F.","Influence of halogen–halogen interactions in the self-assembly of pillar[5]arene-based supramolecular polymers","RSC Advances","2024","14","29","20553","20560","10.1039/D4RA03769C","","","0.71075","MoKα","","0.1935","0.1199","","","0.3487","0.3985","","","","","","1.234","","","","has coordinates,has disorder","292654","2024-06-29","01:12:19","" "7248916","4.7716","0.0001","18.2538","0.0005","16.7147","0.0004","90","","97.171","0.002","90","","1444.46","0.06","150","0.1","150","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 Br N3 O2 -","- C15 H14 Br N3 O2 -","- C60 H56 Br4 N12 O8 -","4","1","","Kotásková, Lucie; Jewula, Pawel; Herchel, Radovan; Nemec, Ivan; Neugebauer, Petr","Photoswitchable hydrazones with pyridine-based rotors and halogen substituents","RSC Advances","2024","14","29","20856","20866","10.1039/D4RA02909G","","x-ray","1.54184","CuKα","","0.037","0.0336","","","0.0918","0.0945","","","","","","1.031","","","","has coordinates","292680","2024-07-02","01:19:51","" "7248917","4.6839","0.0002","18.5687","0.0008","16.9966","0.0006","90","","95.506","0.004","90","","1471.44","0.1","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 I N3 O2 -","- C15 H14 I N3 O2 -","- C60 H56 I4 N12 O8 -","4","1","","Kotásková, Lucie; Jewula, Pawel; Herchel, Radovan; Nemec, Ivan; Neugebauer, Petr","Photoswitchable hydrazones with pyridine-based rotors and halogen substituents","RSC Advances","2024","14","29","20856","20866","10.1039/D4RA02909G","","x-ray","1.54184","CuKα","","0.0583","0.055","","","0.1458","0.1492","","","","","","1.04","","","","has coordinates","292680","2024-07-02","01:19:51","" "7248918","4.6839","0.0002","18.5687","0.0008","16.9966","0.0006","90","","95.506","0.004","90","","1471.44","0.1","100","0.1","100.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 I N3 O2 -","- C15 H14 I N3 O2 -","- C60 H56 I4 N12 O8 -","4","1","","Kotásková, Lucie; Jewula, Pawel; Herchel, Radovan; Nemec, Ivan; Neugebauer, Petr","Photoswitchable hydrazones with pyridine-based rotors and halogen substituents","RSC Advances","2024","14","29","20856","20866","10.1039/D4RA02909G","","","1.54184","CuKα","","0.0572","0.0539","","","0.1424","0.1459","","","","","","1.012","","","","has coordinates","292680","2024-07-02","01:19:51","" "7248919","4.7709","0.0001","18.2539","0.0005","16.7122","0.0004","90","","97.166","0.002","90","","1444.06","0.06","150","0.1","150.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C15 H14 Br N3 O2 -","- C15 H14 Br N3 O2 -","- C60 H56 Br4 N12 O8 -","4","1","","Kotásková, Lucie; Jewula, Pawel; Herchel, Radovan; Nemec, Ivan; Neugebauer, Petr","Photoswitchable hydrazones with pyridine-based rotors and halogen substituents","RSC Advances","2024","14","29","20856","20866","10.1039/D4RA02909G","","","1.54184","CuKα","","0.036","0.0321","","","0.0842","0.0868","","","","","","1.0296","","","","has coordinates","292680","2024-07-02","01:19:51","" "7248920","14.3674","0.001","10.3669","0.0007","10.6054","0.0006","90","","103.165","0.007","90","","1538.11","0.18","121.6","0.5","121.6","","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","(E)-3-(((4H-1,2,4-triazol-4-yl)imino)methyl)-7-(diethylamino)-2H-chromen-2-one","Compound 11","","- C16 H17 N5 O2 -","- C16 H17 N5 O2 -","- C64 H68 N20 O8 -","4","1","","Castro, Geraldyne; Romero-Ávila, Margarita; Farfán, Norberto; Arcos-Ramos, Rafael; Maldonado-Domínguez, Mauricio","Heterocycles as supramolecular handles for crystal engineering: a case study with 7-(diethylamino)coumarin derivatives","RSC Advances","2024","14","29","20824","20836","10.1039/D4RA03656E","","","0.71073","MoKα","","0.0563","0.0422","","","0.1308","0.1474","","","","","","1.0953","","","","has coordinates","292681","2024-07-02","01:20:20","" "7248928","5.0188","0.0006","13.9106","0.0015","25.986","0.003","90","","90","","90","","1814.2","0.4","100","2","100","2","","","","","","","synthesized by authors","4","P 21 21 21","P 2ac 2ab","19","","(E)-4-Styryl-2-(4-(trifluoromethyl)phenyl)quinazoline","","- C23 H15 F3 N2 -","- C23 H15 F3 N2 -","- C92 H60 F12 N8 -","4","1","","Rodríguez, Diego Fernando; Lipez, Kelly Johanna; Stashenko, Elena; Díaz, Iván; Cobo, Justo; Palma, Alirio","Alternative and efficient one-pot three-component synthesis of substituted 2-aryl-4-styrylquinazolines/4-styrylquinazolines from synthetically available 1-(2-aminophenyl)-3-arylprop-2-en-1-ones: characterization and evaluation of their antiproliferative activities","RSC Advances","2024","14","29","20951","20965","10.1039/D4RA03702B","","","0.71073","MoKα","","0.1055","0.0865","","","0.1869","0.1951","","","","","","1.189","","","","has coordinates","292697","2024-07-03","01:10:22","" "7248929","13.1299","0.0008","13.2052","0.0009","7.7725","0.0004","90","","95.083","0.002","90","","1342.32","0.14","100","2","100","2","","","","","","","Synthetic","4","P 1 21/c 1","-P 2ybc","14","","(E)â\/E?4â\/E?(4â\/E?(Trifluoromethyl)styryl)quinazoline","","- C17 H11 F3 N2 -","- C17 H11 F3 N2 -","- C68 H44 F12 N8 -","4","1","","Rodríguez, Diego Fernando; Lipez, Kelly Johanna; Stashenko, Elena; Díaz, Iván; Cobo, Justo; Palma, Alirio","Alternative and efficient one-pot three-component synthesis of substituted 2-aryl-4-styrylquinazolines/4-styrylquinazolines from synthetically available 1-(2-aminophenyl)-3-arylprop-2-en-1-ones: characterization and evaluation of their antiproliferative activities","RSC Advances","2024","14","29","20951","20965","10.1039/D4RA03702B","","","0.71073","MoKα","","0.0802","0.0551","","","0.1173","0.1316","","","","","","1.079","","","","has coordinates","292697","2024-07-03","01:10:23","" "7248930","24.6763","0.0013","3.9753","0.0002","13.3702","0.0007","90","","90","","90","","1311.56","0.12","100","2","100","2","","","","","","","Synthetic","4","P c a 21","P 2c -2ac","29","","(E)–4–(4–Methoxystyryl)quinazoline","","- C17 H14 N2 O -","- C17 H14 N2 O -","- C68 H56 N8 O4 -","4","1","","Rodríguez, Diego Fernando; Lipez, Kelly Johanna; Stashenko, Elena; Díaz, Iván; Cobo, Justo; Palma, Alirio","Alternative and efficient one-pot three-component synthesis of substituted 2-aryl-4-styrylquinazolines/4-styrylquinazolines from synthetically available 1-(2-aminophenyl)-3-arylprop-2-en-1-ones: characterization and evaluation of their antiproliferative activities","RSC Advances","2024","14","29","20951","20965","10.1039/D4RA03702B","","","0.71073","MoKα","","0.0357","0.0314","","","0.0716","0.0741","","","","","","1.045","","","","has coordinates","292697","2024-07-03","01:10:23","" "7248945","4.7711","0.0006","13.43","0.005","19.544","0.002","90","","94.722","0.01","90","","1248","0.5","216","50","216","50","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13.75 H10.75 N O4 -","- C13.75 H10.75 N O4 -","- C55 H43 N4 O16 -","4","1","","Kumar, Sachin; Lal, Bajrang; Singh, Gurleen; Muskan,; Tittal, Ram Kumar; Singh, Jandeep; Vikas D., Ghule; Sharma, Renu","5-Aminoisophthalate-based kojic acid-appended bis-1,2,3-triazole: a fluorescent chemosensor for Cu2+ sensing and in silico study","RSC Advances","2024","14","29","20908","20922","10.1039/D4RA02372B","","x-ray","0.71073","MoKα","","0.0734","0.0567","","","0.1628","0.1805","","","","","","1.077","","","","has coordinates","292725","2024-07-04","01:21:08","" "7248978","9.1191","0.0003","12.1448","0.0007","12.1551","0.0006","76.174","0.004","80.698","0.003","87.947","0.003","1289.97","0.11","293","2","293.15","","","","","","","","","5","P -1","-P 1","2","","","","- C23 H36 O8 S Si -","- C23 H36 O8 S Si -","- C46 H72 O16 S2 Si2 -","2","1","","Yu, Fangzhou; Xu, Liang","A concise and stereoselective synthesis of the BCDF tetracyclic ring system of C19-diterpenoid alkaloids","RSC Advances","2024","14","29","21102","21106","10.1039/D4RA02821J","","x-ray","0.71073","MoKα","","0.1343","0.0922","","","0.2675","0.3068","","","","","","1.058","","","","has coordinates","292746","2024-07-05","01:16:01","" "7248979","13.342","0.0009","8.2734","0.0006","11.9648","0.0008","90","","90","","90","","1320.72","0.16","100","2","100","2","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C6 H13 Cl4 Ga N3 P -","- C6 H13 Cl4 Ga N3 P -","- C24 H52 Cl16 Ga4 N12 P4 -","4","0.5","","Guerriero, Antonella; Ienco, Andrea; Hicks, Thomas; Cilibrizzi, Agostino","Beyond transition block metals: exploring the reactivity of phosphine PTA and its oxide [PTA(O)] towards gallium(iii)","RSC Advances","2024","14","29","21139","21150","10.1039/D4RA02877E","","","1.54178","CuKα","","0.0251","0.0229","","","0.06","0.0603","","","","","","1.102","","","","has coordinates","292747","2024-07-05","01:16:26","" "7248980","13.7699","0.001","8.1328","0.0006","12.1428","0.0009","90","","90","","90","","1359.85","0.17","100","2","100","2","","","","","","","","7","P n m a","-P 2ac 2n","62","","","","- C6 H13 Cl4 Ga N3 O P -","- C6 H13 Cl4 Ga N3 O P -","- C24 H52 Cl16 Ga4 N12 O4 P4 -","4","0.5","","Guerriero, Antonella; Ienco, Andrea; Hicks, Thomas; Cilibrizzi, Agostino","Beyond transition block metals: exploring the reactivity of phosphine PTA and its oxide [PTA(O)] towards gallium(iii)","RSC Advances","2024","14","29","21139","21150","10.1039/D4RA02877E","","","1.54178","CuKα","","0.0424","0.0409","","","0.1108","0.1113","","","","","","1.077","","","","has coordinates","292747","2024-07-05","01:16:27","" "7248981","7.8486","0.0003","9.6385","0.0003","12.779","0.0004","90","","91.652","0.001","90","","966.31","0.06","100","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C6 H13 I N3 O P -","- C6 H13 I N3 O P -","- C24 H52 I4 N12 O4 P4 -","4","1","","Guerriero, Antonella; Ienco, Andrea; Hicks, Thomas; Cilibrizzi, Agostino","Beyond transition block metals: exploring the reactivity of phosphine PTA and its oxide [PTA(O)] towards gallium(iii)","RSC Advances","2024","14","29","21139","21150","10.1039/D4RA02877E","","","0.71073","MoKα","","0.0205","0.0159","","","0.0319","0.0334","","","","","","1.039","","","","has coordinates","292747","2024-07-05","01:16:27","" "7249044","12.3661","0.0006","7.7969","0.0004","7.2005","0.0003","90","","92.93","0.004","90","","693.34","0.06","294","1","294","1","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C H N -","- C1.8 H1.8 -","- C36 H36 -","20","5","","Britto, Kashpar John; Meenakshi, Maniarasu; Srinivasan, Kannupal","Synthesis of 1-aryl-2,3-diaroyl cyclopropanes from 1,3,5-triaryl-1,5-diketones and their transformation into E,E-1,4-diaryl-1,3-butadienes","RSC Advances","2024","14","31","22076","22085","10.1039/D4RA02525C","","x-ray","0.71073","MoKα","","0.0808","0.0539","","","0.1482","0.1719","","","","","","1.055","","","","has coordinates","293403","2024-07-13","01:15:44","" "7249045","7.7597","0.0005","9.1203","0.0005","12.5054","0.0007","102.924","0.004","97.329","0.004","97.611","0.005","843.6","0.09","200","2","200","","","","","","","","","6","P -1","-P 1","2","","","","- C30 H24 Br4 N8 O2 Pb2 -","- C30 H24 Br4 N8 O2 Pb2 -","- C30 H24 Br4 N8 O2 Pb2 -","1","0.5","","Arkak, Akbar; Sadr, Moayad Hossaini; Janghouri, Mohammad; Marandi, Farzin; Fuhrmann, Daniel","1,2,4-triazine derived binuclear lead(ii) complexes: synthesis, spectroscopic and structural investigations and application in organic light-emitting diodes (OLEDs)","RSC Advances","2024","14","30","22006","22016","10.1039/D4RA03383C","","x-ray","0.71073","MoKα","","0.0435","0.0363","","","0.0988","0.1016","","","","","","1.011","","","","has coordinates","293404","2024-07-13","01:15:59","" "7249046","9.7327","0.0006","10.2844","0.0006","10.5326","0.0007","81.463","0.005","68.068","0.005","86.765","0.005","967.13","0.11","200","2","200","","","","","","","","","6","P -1","-P 1","2","","","","- C36 H30 N10 O6 Pb2 S2 -","- C36 H30 N10 O6 Pb2 S2 -","- C36 H30 N10 O6 Pb2 S2 -","1","0.5","","Arkak, Akbar; Sadr, Moayad Hossaini; Janghouri, Mohammad; Marandi, Farzin; Fuhrmann, Daniel","1,2,4-triazine derived binuclear lead(ii) complexes: synthesis, spectroscopic and structural investigations and application in organic light-emitting diodes (OLEDs)","RSC Advances","2024","14","30","22006","22016","10.1039/D4RA03383C","","x-ray","0.71073","MoKα","","0.0348","0.0254","","","0.0556","0.0572","","","","","","0.984","","","","has coordinates","293404","2024-07-13","01:15:59","" "7249048","10.2911","0.0012","10.3975","0.0013","16.635","0.002","94.274","0.004","93.026","0.004","110.473","0.003","1657","0.3","100","2","100","2","","","","","","","","5","P -1","-P 1","2","8d","3,6-Dibromo-2-(4-methoxyphenyl)-7-methyl-8-propylimidazo[1,2-a]pyrimidin-5(8H)-one","","- C17 H17 Br2 N3 O2 -","- C17 H17 Br2 N3 O2 -","- C68 H68 Br8 N12 O8 -","4","2","","Camargo, Delascar; Cifuentes, Carlos; Castillo, Juan-Carlos; Portilla, Jaime","Microwave-assisted synthesis and functionalization of 2-arylimidazo[1,2-a]pyrimidin-5(8H)-ones","RSC Advances","2024","14","31","22368","22373","10.1039/D4RA03948C","","","0.71073","MoKα","","0.1028","0.0761","","","0.209","0.2279","","","","","","1.104","","","","has coordinates","293420","2024-07-16","01:10:07","" "7249049","9.632","0.0002","18.7983","0.0004","19.1207","0.0004","90","","102.451","0.0008","90","","3380.67","0.12","180","","180","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","Butan-1-aminium, N,N,N-tributyl, (TB-5-11)-difluoro(4-methoxyphenyl)diphenylsilicate(1-)","Tetrabutylammonium difluoro(4-methoxyphenyl)diphenylsilicate","","- C35 H53 F2 N O Si -","- C35 H53 F2 N O Si -","- C140 H212 F8 N4 O4 Si4 -","4","1","","Trojan, Michal; Hroch, Adam; Gruden, Evelin; Cvačka, Josef; Čejka, Jan; Tavčar, Gašper; Rybáčková, Markéta; Kvíčala, Jaroslav","Modified aryldifluorophenylsilicates with improved activity and selectivity in nucleophilic fluorination of secondary substrates","RSC Advances","2024","14","31","22326","22334","10.1039/D4RA04332D","","","1.54178","CuKα","","0.0425","0.0393","","0.1119","0.109","0.1119","","","","","","0.9995","","","","has coordinates","293421","2024-07-16","01:10:52","" "7249050","9.6166","0.0003","16.7413","0.0005","20.8563","0.0006","90","","90.7602","0.0011","90","","3357.45","0.17","180","","180","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","Butan-1-aminium, N,N,N-tributyl, (TB-5-11)-difluorodiphenyl[(4-trifluoromethyl)phenyl]silicate(1-)","Tetrabutylammonium difluorodiphenyl[(4-trifluoromethyl)phenyl]silicate","","- C35 H50 F5 N Si -","- C35 H50 F5 N Si -","- C140 H200 F20 N4 Si4 -","4","1","","Trojan, Michal; Hroch, Adam; Gruden, Evelin; Cvačka, Josef; Čejka, Jan; Tavčar, Gašper; Rybáčková, Markéta; Kvíčala, Jaroslav","Modified aryldifluorophenylsilicates with improved activity and selectivity in nucleophilic fluorination of secondary substrates","RSC Advances","2024","14","31","22326","22334","10.1039/D4RA04332D","","","0.71073","MoKα","","0.0617","0.0458","","0.1229","0.0973","0.1194","","","","","","1","","","","has coordinates","293421","2024-07-16","01:10:54","" "7249051","9.4251","0.0003","20.4233","0.0007","18.7305","0.0006","90","","103.315","0.0017","90","","3508.6","0.2","180","","180","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","Butan-1-aminium, N,N,N-tributyl, (TB-5-11)-difluorobis(4-methoxyphenyl)phenylsilicate(1-)","Tetrabutylammonium difluorobis(4-methoxyphenyl)phenylsilicate","","- C36 H55 F2 N O2 Si -","- C36 H55 F2 N O2 Si -","- C144 H220 F8 N4 O8 Si4 -","4","1","","Trojan, Michal; Hroch, Adam; Gruden, Evelin; Cvačka, Josef; Čejka, Jan; Tavčar, Gašper; Rybáčková, Markéta; Kvíčala, Jaroslav","Modified aryldifluorophenylsilicates with improved activity and selectivity in nucleophilic fluorination of secondary substrates","RSC Advances","2024","14","31","22326","22334","10.1039/D4RA04332D","","","1.54178","CuKα","","0.0915","0.08","","0.2311","0.2223","0.2311","","","","","","1.0002","","","","has coordinates","293421","2024-07-16","01:11:03","" "7249070","14.941","0.002","30.117","0.005","8.434","0.0013","90","","102.447","0.004","90","","3705.9","1","273.15","","273.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C3.158 H1.965 Cl0.281 N0.281 O0.07 -","- C3.15789 H1.96491 Cl0.280702 N0.280702 O0.0701754 -","- C180 H112 Cl16 N16 O4 -","57","14.25","","Li, Tian-Miao; Hu, Li-Yuan; Zou, Xin; Wang, Jun-Yi; Ni, Sheng; Liu, Lei; Xiao, Xunwen; Luo, Xu-Feng","Hybridization of short-range and long-range charge transfer boosts room-temperature phosphorescence performance","RSC Advances","2024","14","31","22763","22768","10.1039/D4RA03283G","","","0.71073","MoKα","","0.1401","0.0669","","","0.1505","0.1968","","","","","","1.1164","","","","has coordinates","293468","2024-07-19","01:15:50","" "7249071","8.565","0.003","15.216","0.006","30.113","0.011","90","","90","","103.425","0.009","3817","2","273.15","","273.15","","","","","","","","","4","P -1","-P 1","2","","","","- C2.847 H1.424 Br0.271 N0.203 -","- C2.84746 H1.42373 Br0.271186 N0.20339 -","- C168 H84 Br16 N12 -","59","29.5","","Li, Tian-Miao; Hu, Li-Yuan; Zou, Xin; Wang, Jun-Yi; Ni, Sheng; Liu, Lei; Xiao, Xunwen; Luo, Xu-Feng","Hybridization of short-range and long-range charge transfer boosts room-temperature phosphorescence performance","RSC Advances","2024","14","31","22763","22768","10.1039/D4RA03283G","","","0.71073","MoKα","","0.3125","0.0795","","","0.123","0.2066","","","","","","0.9919","","","","has coordinates","293468","2024-07-19","01:15:53","" "7249072","6.0338","0.0001","7.3549","0.0002","20.9236","0.0005","85.352","0.002","88.35","0.002","73.647","0.002","888.04","0.04","126","","126","","","","","","","","","5","P -1","-P 1","2","","ANC-5","","- C21 H19 F N6 O -","- C21 H19 F N6 O -","- C42 H38 F2 N12 O2 -","2","1","","Khetmalis, Yogesh Mahadu; Shobha, Singarapalle; Nandikolla, Adinarayana; Chandu, Ala; Murugesan, Sankaranarayanan; Kumar, Muthyala Murali Krishna; Chandra Sekhar, Kondapalli Venkata Gowri","Design, synthesis, and anti-mycobacterial evaluation of 1,8-naphthyridine-3-carbonitrile analogues","RSC Advances","2024","14","31","22676","22689","10.1039/D4RA04262J","","x-ray","1.54184","CuKα","","0.0496","0.0461","","","0.1299","0.1328","","","","","","1.093","","","","has coordinates","293469","2024-07-19","01:16:13","" "7249083","6.845","0.0007","7.2531","0.0008","15.6037","0.0017","95.832","0.003","98.967","0.003","108.964","0.003","714","0.13","293","2","293","2","","","","","","","","4","P -1","-P 1","2","","","","- C2.14 H2.29 N0.29 O0.71 -","- C2.14286 H2.28571 N0.285714 O0.714286 -","- C30 H32 N4 O10 -","14","7","","Kumar, Ram; Singh, Bholey; Gahlyan, Parveen; Verma, Abhishek; Bhandari, Mamta; Kakkar, Rita; Pani, Balaram","An innovative Schiff-base colorimetric chemosensor for the selective detection of Cu2+ ions and its applications","RSC Advances","2024","14","32","23083","23094","10.1039/D4RA03097D","","","0.71073","MoKα","","0.0915","0.0746","","","0.1625","0.1762","","","","","","1.089","","","","has coordinates","293504","2024-07-23","01:13:09","" "7249131","15.6222","0.0001","11.8985","0.0001","19.7101","0.0001","90","","105.198","0.001","90","","3535.59","0.04","100","2","100","2","","","","","","","","5","I 1 2/a 1","-I 2ya","15","","","","- C47 H36 N2 O2 S2 -","- C47 H36 N2 O2 S2 -","- C188 H144 N8 O8 S8 -","4","0.5","","Younes, Eyad A.; AL-Snaid, Amneh M.; Abu-Safieh, Kayed A.; Salami, Fatemeh; Aljaar, Nayyef; Zhao, Yuming","Synthesis and characterization of 2-(anthracene-9-yl)-4,5-diphenyl-1H-imidazole derivatives as environmentally sensitive fluorophores","RSC Advances","2024","14","32","23511","23519","10.1039/D4RA03735A","","x-ray","1.54184","CuKα","","0.0393","0.0386","","","0.0956","0.096","","","","","","1.04","","","","has coordinates,has disorder","293578","2024-07-28","01:15:13","" "7249132","15.5732","0.0003","11.1891","0.0003","28.367","0.0006","90","","90","","90","","4942.95","0.19","293","2","293","2","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C30 H20 Br2 N2 -","- C30 H20 Br2 N2 -","- C240 H160 Br16 N16 -","8","2","","Younes, Eyad A.; AL-Snaid, Amneh M.; Abu-Safieh, Kayed A.; Salami, Fatemeh; Aljaar, Nayyef; Zhao, Yuming","Synthesis and characterization of 2-(anthracene-9-yl)-4,5-diphenyl-1H-imidazole derivatives as environmentally sensitive fluorophores","RSC Advances","2024","14","32","23511","23519","10.1039/D4RA03735A","","x-ray","1.54184","CuKα","","0.0548","0.0471","","","0.129","0.1448","","","","","","1.093","","","","has coordinates","293578","2024-07-28","01:15:14","" "7249133","11.5722","0.0001","13.9231","0.0002","24.5599","0.0003","91.477","0.001","94.074","0.001","99.887","0.001","3885.59","0.08","100","2","100","2","","","","","","","","4","P -1","-P 1","2","","","","- C45 H28 N2 S2 -","- C45 H28 N2 S2 -","- C180 H112 N8 S8 -","4","2","","Younes, Eyad A.; AL-Snaid, Amneh M.; Abu-Safieh, Kayed A.; Salami, Fatemeh; Aljaar, Nayyef; Zhao, Yuming","Synthesis and characterization of 2-(anthracene-9-yl)-4,5-diphenyl-1H-imidazole derivatives as environmentally sensitive fluorophores","RSC Advances","2024","14","32","23511","23519","10.1039/D4RA03735A","","x-ray","1.54184","CuKα","","0.0481","0.0432","","","0.1043","0.107","","","","","","1.065","","","","has coordinates","293578","2024-07-28","01:15:14","" "7249134","14.3775","0.0001","15.7779","0.0002","23.0024","0.0002","84.715","0.001","78.893","0.001","72.816","0.001","4888.27","0.09","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C29.9 H19.4 Br2 Cl0.2 N2.4 -","- C29.902 H19.402 Br2 Cl0.196 N2.402 -","- C239.216 H155.216 Br16 Cl1.568 N19.216 -","8","4","","Younes, Eyad A.; AL-Snaid, Amneh M.; Abu-Safieh, Kayed A.; Salami, Fatemeh; Aljaar, Nayyef; Zhao, Yuming","Synthesis and characterization of 2-(anthracene-9-yl)-4,5-diphenyl-1H-imidazole derivatives as environmentally sensitive fluorophores","RSC Advances","2024","14","32","23511","23519","10.1039/D4RA03735A","","x-ray","1.54184","CuKα","","0.0536","0.0455","","","0.1087","0.1139","","","","","","1.055","","","","has coordinates,has disorder","293578","2024-07-28","01:15:14","" "7249161","7.621","0.0014","10.7471","0.0018","24.768","0.004","90","","90","","90","","2028.6","0.6","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","[RuCl(p-cymene)(1-ClPh-3-Pyridiltriazenide)]","","- C21 H22 Cl2 N4 Ru -","- C21 H22 Cl2 N4 Ru -","- C84 H88 Cl8 N16 Ru4 -","4","1","","Romero-Soto, Christian A.; Iglesias, Ana L.; Velázquez-Ham, Amor F.; Camarena-Díaz, Juan P.; Correa-Ayala, Erick; Gomez-Lopez, Jessica L.; Chávez, Daniel; Ochoa-Terán, Adrián; Aguirre, Gerardo; Rheingold, Arnold L.; Grotjahn, Douglas B.; Parra-Hake, Miguel; Miranda-Soto, Valentín","Ruthenium complexes with triazenide ligands bearing an N-heterocyclic moiety, and their catalytic properties in the reduction of nitroarenes","RSC Advances","2024","14","33","24019","24030","10.1039/D4RA04813J","","","0.71073","MoKα","","0.0409","0.0329","","","0.0578","0.0601","","","","","","1.037","","","","has coordinates","293615","2024-08-01","01:25:49","" "7249162","7.9615","0.0001","11.8552","0.0001","25.7291","0.0002","90","","90","","90","","2428.45","0.04","293.4","0.3","293.4","0.3","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","RuCl-triazenide-Quinoline","[RuCl(1-ClPh-3-quinolinetriazenide)(p-cymene)]","","- C25 H24 Cl2 N4 Ru -","- C25 H24 Cl2 N4 Ru -","- C100 H96 Cl8 N16 Ru4 -","4","1","","Romero-Soto, Christian A.; Iglesias, Ana L.; Velázquez-Ham, Amor F.; Camarena-Díaz, Juan P.; Correa-Ayala, Erick; Gomez-Lopez, Jessica L.; Chávez, Daniel; Ochoa-Terán, Adrián; Aguirre, Gerardo; Rheingold, Arnold L.; Grotjahn, Douglas B.; Parra-Hake, Miguel; Miranda-Soto, Valentín","Ruthenium complexes with triazenide ligands bearing an N-heterocyclic moiety, and their catalytic properties in the reduction of nitroarenes","RSC Advances","2024","14","33","24019","24030","10.1039/D4RA04813J","","x-ray","1.54184","CuKα","","0.0321","0.0309","","","0.0779","0.0787","","","","","","1.043","","","","has coordinates","293615","2024-08-01","01:25:51","" "7249163","20.5077","0.0012","7.6529","0.0003","26.1253","0.0017","90","","90","","90","","4100.2","0.4","293","2","293","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C21 H22 Cl2 N4 Ru -","- C21 H22 Cl2 N4 Ru -","- C168 H176 Cl16 N32 Ru8 -","8","1","","Romero-Soto, Christian A.; Iglesias, Ana L.; Velázquez-Ham, Amor F.; Camarena-Díaz, Juan P.; Correa-Ayala, Erick; Gomez-Lopez, Jessica L.; Chávez, Daniel; Ochoa-Terán, Adrián; Aguirre, Gerardo; Rheingold, Arnold L.; Grotjahn, Douglas B.; Parra-Hake, Miguel; Miranda-Soto, Valentín","Ruthenium complexes with triazenide ligands bearing an N-heterocyclic moiety, and their catalytic properties in the reduction of nitroarenes","RSC Advances","2024","14","33","24019","24030","10.1039/D4RA04813J","","x-ray","0.71073","MoKα","","0.0693","0.0425","","","0.0769","0.0847","","","","","","1.077","","","","has coordinates","293615","2024-08-01","01:25:52","" "7249164","12.9896","0.0004","13.2753","0.0004","14.0569","0.0004","90","0.003","116.179","0.003","90","0.003","2175.33","0.13","293.1","1","293.1","1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","RuCl-ImidazoleTriazenide","[RuCl(1-MePh-3-imidazoletriazenide)(p-cymene)]","","- C21 H26 Cl N5 Ru -","- C21 H26 Cl N5 Ru -","- C84 H104 Cl4 N20 Ru4 -","4","1","","Romero-Soto, Christian A.; Iglesias, Ana L.; Velázquez-Ham, Amor F.; Camarena-Díaz, Juan P.; Correa-Ayala, Erick; Gomez-Lopez, Jessica L.; Chávez, Daniel; Ochoa-Terán, Adrián; Aguirre, Gerardo; Rheingold, Arnold L.; Grotjahn, Douglas B.; Parra-Hake, Miguel; Miranda-Soto, Valentín","Ruthenium complexes with triazenide ligands bearing an N-heterocyclic moiety, and their catalytic properties in the reduction of nitroarenes","RSC Advances","2024","14","33","24019","24030","10.1039/D4RA04813J","","x-ray","0.71073","MoKα","","0.0393","0.029","","","0.0644","0.0691","","","","","","1.066","","","","has coordinates","293615","2024-08-01","01:25:52","" "7249165","9.8885","0.0008","14.1476","0.0011","17.6592","0.0011","102.034","0.006","100.332","0.007","94.941","0.007","2357.4","0.3","294.7","0.7","294.7","0.7","","","","","","","","5","P -1","-P 1","2","","","","- C25 H24 Cl2 N4 Ru -","- C25 H24 Cl2 N4 Ru -","- C100 H96 Cl8 N16 Ru4 -","4","2","","Romero-Soto, Christian A.; Iglesias, Ana L.; Velázquez-Ham, Amor F.; Camarena-Díaz, Juan P.; Correa-Ayala, Erick; Gomez-Lopez, Jessica L.; Chávez, Daniel; Ochoa-Terán, Adrián; Aguirre, Gerardo; Rheingold, Arnold L.; Grotjahn, Douglas B.; Parra-Hake, Miguel; Miranda-Soto, Valentín","Ruthenium complexes with triazenide ligands bearing an N-heterocyclic moiety, and their catalytic properties in the reduction of nitroarenes","RSC Advances","2024","14","33","24019","24030","10.1039/D4RA04813J","","x-ray","0.71073","MoKα","","0.1921","0.0923","","","0.1928","0.2474","","","","","","1.022","","","","has coordinates","293615","2024-08-01","01:25:52","" "7249166","6.54533","0.00013","29.5464","0.0005","7.4552","0.0002","90","","101.691","0.002","90","","1411.86","0.05","294.1","0.4","294.1","0.4","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","3-(4-chlorophenyl)-5-(p-tolyl)-6H-1,2-oxazin-6-one","","- C17 H12 Cl N O2 -","- C17 H12 Cl N O2 -","- C68 H48 Cl4 N4 O8 -","4","1","","Alcántar-Zavala, Eleazar; Delgado-Vargas, Francisco; Marín-González, Fabricio; Angulo, Gabriela López; Aguirre-Madrigal, Hugo Enrique; Ochoa-Terán, Adrián; Rodríguez-Vega, Gibrán; Aguirre-Hernández, Gerardo; Montes-Avila, Julio","Design, synthesis, and exploration of antibacterial activity of 6H-1,2-oxazin-6-ones.","RSC advances","2024","14","33","23828","23839","10.1039/d4ra04220d","","x-ray","1.54184","CuKα","","0.0554","0.0451","","","0.1197","0.1273","","","","","","1.036","","","","has coordinates","293616","2024-08-01","01:26:15","" "7249167","5.0224","0.0007","13.54","0.002","21.561","0.003","90","","90","","90","","1466.2","0.4","293","2","293","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","3-(4-methoxyphenyl)-5-(p-tolyl)-6H-1,2-oxazin-6-one","","- C18 H15 N O3 -","- C18 H15 N O3 -","- C72 H60 N4 O12 -","4","1","","Alcántar-Zavala, Eleazar; Delgado-Vargas, Francisco; Marín-González, Fabricio; Angulo, Gabriela López; Aguirre-Madrigal, Hugo Enrique; Ochoa-Terán, Adrián; Rodríguez-Vega, Gibrán; Aguirre-Hernández, Gerardo; Montes-Avila, Julio","Design, synthesis, and exploration of antibacterial activity of 6H-1,2-oxazin-6-ones.","RSC advances","2024","14","33","23828","23839","10.1039/d4ra04220d","","x-ray","0.71073","MoKα","","0.1102","0.0566","","","0.1212","0.1471","","","","","","1.049","","","","has coordinates","293616","2024-08-01","01:26:16","" "7249168","11.438","0.012","25.58","0.03","4.893","0.005","90","","90","","90","","1432","3","296","2","296","2","","","","","","","","4","P n m a","-P 2ac 2n","62","","","","- C15 H12 Br2 N2 -","- C15 H12 Br2 N2 -","- C60 H48 Br8 N8 -","4","0.5","","Wang, Zhongjie; He, Yu; Wang, Fang; Wang, Yan; Luo, Hui; Wu, Jianglong; Yang, Jinhui","Green and efficient synthesis of dibenzyl cyanamides and ureas with cyanamide as a block.","RSC advances","2024","14","33","23693","23698","10.1039/d4ra04286g","","","0.71073","MoKα","","0.0547","0.0298","","","0.0569","0.0626","","","","","","1.068","","","","has coordinates","293617","2024-08-01","01:26:49","" "7249169","9.0138","0.0008","13.9046","0.0014","11.9428","0.0013","90","","100.927","0.002","90","","1469.7","0.3","296","2","296","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 N4 O4 -","- C15 H12 N4 O4 -","- C60 H48 N16 O16 -","4","1","","Wang, Zhongjie; He, Yu; Wang, Fang; Wang, Yan; Luo, Hui; Wu, Jianglong; Yang, Jinhui","Green and efficient synthesis of dibenzyl cyanamides and ureas with cyanamide as a block.","RSC advances","2024","14","33","23693","23698","10.1039/d4ra04286g","","","0.71073","MoKα","","0.1639","0.0638","","","0.1276","0.1693","","","","","","0.991","","","","has coordinates","293617","2024-08-01","01:26:49","" "7249170","11.6329","0.0006","7.7767","0.0005","29.3752","0.0018","90","","90","","90","","2657.4","0.3","296","2","296","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C15 H14 F2 N2 O -","- C15 H14 F2 N2 O -","- C120 H112 F16 N16 O8 -","8","1","","Wang, Zhongjie; He, Yu; Wang, Fang; Wang, Yan; Luo, Hui; Wu, Jianglong; Yang, Jinhui","Green and efficient synthesis of dibenzyl cyanamides and ureas with cyanamide as a block.","RSC advances","2024","14","33","23693","23698","10.1039/d4ra04286g","","","0.71073","MoKα","","0.0759","0.0508","","","0.109","0.1202","","","","","","1.033","","","","has coordinates","293617","2024-08-01","01:26:50","" "7249178","9.7669","0.0005","10.7587","0.0008","18.6574","0.0014","90","","90","","90","","1960.5","0.2","293","2","293","2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C25 H19 N3 O2 -","- C25 H19 N3 O2 -","- C100 H76 N12 O8 -","4","1","","Nguyen, Nguyen Tran; Dai, Vo Viet; Mechler, Adam; Van Meervelt, Luc; Hoa, Nguyen Thi; Vo, Quan V.","Synthesis and computational evaluation of the antioxidant activity of pyrrolo[2,3-b]quinoxaline derivatives","RSC Advances","2024","14","34","24438","24446","10.1039/D4RA03108C","","x-ray","0.71073","MoKα","","0.0682","0.0474","","","0.0942","0.1066","","","","","","1.073","","","","has coordinates","293963","2024-08-06","01:20:10","" "7249183","11.3518","0.0003","15.4233","0.0004","26.8182","0.0006","89.06","0.002","85.478","0.002","89.87","0.002","4680.1","0.2","130","","130","","","","","","","","","7","P -1","-P 1","2","","","","- C108 H120.13 Cl3 Fe3 O3 P3 Rh3 -","- C108 H120.132 Cl3 Fe3 O3 P3 Rh3 -","- C216 H240.264 Cl6 Fe6 O6 P6 Rh6 -","2","1","","Straube, Axel; Coburger, Peter; Hey-Hawkins, Evamarie","Homotrinuclear ruthenium(ii) and rhodium(i) complexes of redox-active tris(ferrocenyl)arene-based tris-phosphanes.","RSC advances","2024","14","34","24652","24660","10.1039/d4ra03822c","","","0.71073","MoKα","","0.0938","0.0588","","","0.1057","0.118","","","","","","1.05","","","","has coordinates,has disorder","294049","2024-08-08","01:15:42","" "7249184","18.2645","0.0005","9.2078","0.0002","9.6666","0.0002","90","","90","","90","","1625.69","0.07","295","","295","","","","","","","","","3","P c a 21","P 2c -2ac","29","","","","- C20 H20 O3 -","- C20 H20 O3 -","- C80 H80 O12 -","4","1","","Sayad, Rayene; Bouzina, Abdeslem; Bouone, Yousra Ouafa; Beldjezzia, Dounia; Djemel, Abdelhak; Ibrahim-Ouali, Malika; Aouf, Nour-Eddine; Aouf, Zineb","Zinc acetate-catalyzed, green and efficient synthesis of xanthene derivatives under ultrasound irradiation: X-ray crystallographic analysis and in silico study.","RSC advances","2024","14","34","24585","24603","10.1039/d4ra04135f","","x-ray","1.54184","CuKα","","0.0555","0.0424","","","0.101","0.1106","","","","","","1.045","","","","has coordinates","294050","2024-08-08","01:16:05","" "7249194","14.9621","0.0017","17.7063","0.0018","18.5333","0.0012","75.538","0.008","89.907","0.008","73.826","0.01","4554","0.8","298","2","298","2","","","","","","","","4","P -1","-P 1","2","","","","- C19 H14 N2 O -","- C19 H14 N2 O -","- C228 H168 N24 O12 -","12","6","","Hurtado-Rodríguez, Diana; Becerra, Diana; Rojas, Hugo; Gómez Castaño, Jovanny A.; Macías, Mario A.; Castillo, Juan-Carlos","Crystal structure, spectroscopy, DFT, and thermal studies of 3-cyano-2(1H)-pyridones as potential anticancer agents","RSC Advances","2024","14","34","24928","24941","10.1039/D4RA04563G","","","1.54184","CuKα","","0.1519","0.087","","","0.2297","0.3109","","","","","","0.999","","","","has coordinates","294089","2024-08-13","01:17:33","" "7249195","18.7005","0.0014","14.5206","0.0012","34.471","0.002","90","","104.606","0.008","90","","9057.8","1.2","298","2","298","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H11 Br N2 O -","- C18 H11 Br N2 O -","- C432 H264 Br24 N48 O24 -","24","6","","Hurtado-Rodríguez, Diana; Becerra, Diana; Rojas, Hugo; Gómez Castaño, Jovanny A.; Macías, Mario A.; Castillo, Juan-Carlos","Crystal structure, spectroscopy, DFT, and thermal studies of 3-cyano-2(1H)-pyridones as potential anticancer agents","RSC Advances","2024","14","34","24928","24941","10.1039/D4RA04563G","","","1.54184","CuKα","","0.1406","0.1039","","","0.3029","0.3747","","","","","","1.06","","","","has coordinates,has disorder","294089","2024-08-13","01:17:36","" "7249196","14.4943","0.0009","17.848","0.0009","18.7119","0.0008","106.539","0.004","90.018","0.005","105.413","0.005","4458.4","0.4","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H11 Cl N2 O -","- C18 H11 Cl N2 O -","- C216 H132 Cl12 N24 O12 -","12","6","","Hurtado-Rodríguez, Diana; Becerra, Diana; Rojas, Hugo; Gómez Castaño, Jovanny A.; Macías, Mario A.; Castillo, Juan-Carlos","Crystal structure, spectroscopy, DFT, and thermal studies of 3-cyano-2(1H)-pyridones as potential anticancer agents","RSC Advances","2024","14","34","24928","24941","10.1039/D4RA04563G","","","1.54184","CuKα","","0.1017","0.0758","","","0.2062","0.2367","","","","","","1.024","","","","has coordinates,has disorder","294089","2024-08-13","01:17:37","" "7249197","4.8146","0.0004","20.525","0.002","21.556","0.003","90","","90.453","0.005","90","","2130.1","0.4","150","2","150","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C28 H20 O2 S2 -","- C28 H20 O2 S2 -","- C112 H80 O8 S8 -","4","1","","Adusei, Emmanuel B. A.; Casetti, Vincent T.; Goldsmith, Calvin D.; Caswell, Madison; Alinj, Drecila; Park, Jimin; Zeller, Matthias; Rusakov, Alexander A.; Kinney, Zacharias J.","Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores","RSC Advances","2024","14","35","25120","25129","10.1039/D4RA04850D","","","0.71073","MoKα","","0.075","0.0425","","","0.0954","0.1081","","","","","","1.028","","","","has coordinates,has disorder","294091","2024-08-13","01:18:29","" "7249198","13.7285","0.0009","7.9848","0.0005","21.6165","0.0014","90","","100.332","0.003","90","","2331.2","0.3","150","2","150","2","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C30 H24 O2 S2 -","- C30 H24 O2 S2 -","- C120 H96 O8 S8 -","4","1","","Adusei, Emmanuel B. A.; Casetti, Vincent T.; Goldsmith, Calvin D.; Caswell, Madison; Alinj, Drecila; Park, Jimin; Zeller, Matthias; Rusakov, Alexander A.; Kinney, Zacharias J.","Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores","RSC Advances","2024","14","35","25120","25129","10.1039/D4RA04850D","","","0.71073","MoKα","","0.0719","0.0444","","","0.1049","0.12","","","","","","1.024","","","","has coordinates","294091","2024-08-13","01:18:30","" "7249199","8.7673","0.0007","6.2302","0.0004","25.9473","0.0019","90","","93.533","0.003","90","","1414.6","0.18","150","2","150","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C34 H32 O5 S2 -","- C34 H32 O5 S2 -","- C68 H64 O10 S4 -","2","1","","Adusei, Emmanuel B. A.; Casetti, Vincent T.; Goldsmith, Calvin D.; Caswell, Madison; Alinj, Drecila; Park, Jimin; Zeller, Matthias; Rusakov, Alexander A.; Kinney, Zacharias J.","Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores","RSC Advances","2024","14","35","25120","25129","10.1039/D4RA04850D","","","0.71073","MoKα","","0.0333","0.0312","","","0.0858","0.0871","","","","","","1.049","","","","has coordinates","294091","2024-08-13","01:18:31","" "7249200","17.861","0.005","8.2438","0.0016","18.565","0.004","90","","111.359","0.007","90","","2545.8","1","150","2","150","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H18 F6 O2 S2 -","- C30 H18 F6 O2 S2 -","- C120 H72 F24 O8 S8 -","4","1","","Adusei, Emmanuel B. A.; Casetti, Vincent T.; Goldsmith, Calvin D.; Caswell, Madison; Alinj, Drecila; Park, Jimin; Zeller, Matthias; Rusakov, Alexander A.; Kinney, Zacharias J.","Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores","RSC Advances","2024","14","35","25120","25129","10.1039/D4RA04850D","","","0.71073","MoKα","","0.1142","0.0531","","","0.1137","0.14","","","","","","1.008","","","","has coordinates,has disorder","294091","2024-08-13","01:18:31","" "7249201","41.918","0.003","26.6997","0.0019","15.3487","0.0011","90","","104.041","0.002","90","","16665","2","150","2","150","2","","","","","","","","4","C 1 2/c 1","-C 2yc","15","","","","- C38 H40 O2 S2 -","- C37.9975 H39.9945 O2 S2 -","- C607.96 H639.912 O32 S32 -","16","2","","Adusei, Emmanuel B. A.; Casetti, Vincent T.; Goldsmith, Calvin D.; Caswell, Madison; Alinj, Drecila; Park, Jimin; Zeller, Matthias; Rusakov, Alexander A.; Kinney, Zacharias J.","Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores","RSC Advances","2024","14","35","25120","25129","10.1039/D4RA04850D","","","0.71073","MoKα","","0.1257","0.0774","","","0.2225","0.2622","","","","","","1.031","","","","has coordinates,has disorder","294091","2024-08-13","01:18:31","" "7249202","7.6349","0.0007","8.9698","0.001","11.0037","0.0012","106.884","0.01","97.904","0.009","110.288","0.009","652.1","0.14","125.8","0.3","125.8","0.3","","","","","","","","5","P -1","-P 1","2","","","","- C20 H30 Cl4 Co N12 -","- C20 H30 Cl4 Co N12 -","- C20 H30 Cl4 Co N12 -","1","0.5","","Jabeur, Wiem; Korb, Marcus; Hamdi, Mohamed; Holub, Mariia; Princík, Dávid; Zeleňák, Vladimír; Sanchez-Coronilla, Antonio; Shalash, Marwan; Čižmár, Erik; Naïli, Houcine","Structural, optical and magnetic properties of a new metal–organic CoII-based complex","RSC Advances","2024","14","34","25048","25061","10.1039/D4RA02149E","","","0.71073","MoKα","","0.0671","0.0591","","","0.1528","0.1606","","","","","","1.044","","","","has coordinates","294092","2024-08-13","01:18:51","" "7249214","12.697","0.0011","16.0824","0.0015","18.3656","0.0016","90","","94.885","0.003","90","","3736.6","0.6","100.07","","100.07","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C38 H47 Cu N5 O8 -","- C38 H47 Cu N5 O8 -","- C152 H188 Cu4 N20 O32 -","4","1","","Tella, Adedibu C.; Olatunji, Sunday J.; Ajibade, Peter A.","Functionalization of a porous copper(ii) metal–organic framework and its capacity for loading and delivery of ibuprofen","RSC Advances","2024","14","35","25759","25770","10.1039/D4RA03678F","","","1.54178","CuKα","","0.0505","0.0465","","","0.1292","0.1309","","","","","","1.017","","","","has coordinates","294148","2024-08-16","01:22:46","" "7249215","9.0416","0.0003","20.2173","0.0005","22.2247","0.0006","90","","90","","90","","4062.6","0.2","99.97","0.13","99.97","0.13","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C17 H16 O3 -","- C17 H16 O3 -","- C204 H192 O36 -","12","3","","Zhang, Yu; Yu, Yueyang; Ma, Xiaoqiang; Zhao, Xiaofei; Huang, Jialin; Zhao, Depeng","Conformational studies of biaryl-bridged seven-membered lactones with a quaternary carbon center.","RSC advances","2024","14","35","25663","25668","10.1039/d4ra04703f","","x-ray","1.54184","CuKα","","0.0881","0.0734","","","0.1726","0.2089","","","","","","1.139","","","","has coordinates","294149","2024-08-16","01:23:14","" "7249216","8.339","0.0004","11.1632","0.0006","16.2872","0.0007","90","","93.877","0.004","90","","1512.7","0.13","100","0.1","100","0.1","","","","","","","","3","P 1 21/n 1","-P 2yn","14","","","","- C19 H20 O3 -","- C19 H20 O3 -","- C76 H80 O12 -","4","1","","Zhang, Yu; Yu, Yueyang; Ma, Xiaoqiang; Zhao, Xiaofei; Huang, Jialin; Zhao, Depeng","Conformational studies of biaryl-bridged seven-membered lactones with a quaternary carbon center.","RSC advances","2024","14","35","25663","25668","10.1039/d4ra04703f","","x-ray","1.54184","CuKα","","0.1159","0.109","","","0.322","0.3254","","","","","","1.249","","","","has coordinates","294149","2024-08-16","01:23:14","" "7249217","7.9631","0.0001","9.0415","0.0001","19.8923","0.0001","90","","90","","90","","1432.21","0.03","100","0.1","100","0.1","","","","","","","","3","P 21 21 21","P 2ac 2ab","19","","","","- C18 H18 O3 -","- C18 H18 O3 -","- C72 H72 O12 -","4","1","","Zhang, Yu; Yu, Yueyang; Ma, Xiaoqiang; Zhao, Xiaofei; Huang, Jialin; Zhao, Depeng","Conformational studies of biaryl-bridged seven-membered lactones with a quaternary carbon center.","RSC advances","2024","14","35","25663","25668","10.1039/d4ra04703f","","x-ray","1.54184","CuKα","","0.0289","0.0281","","","0.0741","0.0745","","","","","","1.049","","","","has coordinates","294149","2024-08-16","01:23:15","" "7249224","10.6343","0.0007","30.9675","0.0018","12.5823","0.0008","90","","110.817","0.002","90","","3873.1","0.4","173","2","173","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C37 H48 Cl2 N6 O2 Ti -","- C37 H48 Cl2 N6 O2 Ti -","- C148 H192 Cl8 N24 O8 Ti4 -","4","1","","Flores-Romero, Víctor; LeBlanc, Jesse; Chen, Zichuan; Lavoie, Gino G.","Ti and Zr complexes bearing guanidine-phenolate ligands: coordination chemistry and polymerization studies","RSC Advances","2024","14","35","25889","25899","10.1039/D4RA05146G","","","0.71073","MoKα","","0.07","0.06","","","0.1306","0.1352","","","","","","1.191","","","","has coordinates,has disorder","294166","2024-08-18","01:01:22","" "7249225","14.5172","0.0008","11.584","0.0006","19.1268","0.001","90","","90","","90","","3216.5","0.3","173","2","173","","","","","","","","","5","P c a 21","P 2c -2ac","29","","","","- C30 H46 N6 O4 Ti -","- C30 H46 N6 O4 Ti -","- C120 H184 N24 O16 Ti4 -","4","1","","Flores-Romero, Víctor; LeBlanc, Jesse; Chen, Zichuan; Lavoie, Gino G.","Ti and Zr complexes bearing guanidine-phenolate ligands: coordination chemistry and polymerization studies","RSC Advances","2024","14","35","25889","25899","10.1039/D4RA05146G","","","0.71073","MoKα","","0.0924","0.0481","","","0.1066","0.1296","","","","","","1.053","","","","has coordinates","294166","2024-08-18","01:01:23","" "7249226","9.6548","0.0004","15.7838","0.0006","19.7193","0.0007","90","","90.246","0.002","90","","3005","0.2","173","2","173","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H42 N6 O4 Zr -","- C28 H42 N6 O4 Zr -","- C112 H168 N24 O16 Zr4 -","4","1","","Flores-Romero, Víctor; LeBlanc, Jesse; Chen, Zichuan; Lavoie, Gino G.","Ti and Zr complexes bearing guanidine-phenolate ligands: coordination chemistry and polymerization studies","RSC Advances","2024","14","35","25889","25899","10.1039/D4RA05146G","","","0.71073","MoKα","","0.0976","0.058","","","0.0979","0.1126","","","","","","1.049","","","","has coordinates","294166","2024-08-18","01:01:23","" "7249227","23.2014","0.0007","10.7004","0.0003","24.3975","0.0007","90","","95.7949","0.0012","90","","6026.1","0.3","173","","173","","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C28 H42 N6 O4 Ti -","- C28 H42 N6 O4 Ti -","- C224 H336 N48 O32 Ti8 -","8","2","","Flores-Romero, Víctor; LeBlanc, Jesse; Chen, Zichuan; Lavoie, Gino G.","Ti and Zr complexes bearing guanidine-phenolate ligands: coordination chemistry and polymerization studies","RSC Advances","2024","14","35","25889","25899","10.1039/D4RA05146G","","","0.71073","MoKα","","0.0643","0.0532","","","0.1254","0.1316","","","","","","1.131","","","","has coordinates,has disorder","294166","2024-08-18","01:01:23","" "7249242","9.578","0.0003","16.2412","0.0006","33.3733","0.0012","90","","96.353","0.001","90","","5159.6","0.3","145","2","145","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H26 I2 N4 Pd -","- C24 H26 I2 N4 Pd -","- C192 H208 I16 N32 Pd8 -","8","2","","Joshi, Om Prakash; Thirumoorthi, Ramalingam; Pardasani, Ram T.; Ray, Sriparna; Dash, Chandrakanta","Palladium(ii) complexes bearing mesoionic carbene ligands: catalytic application in domino Sonogashira coupling/cyclization reactions for one-pot synthesis of benzofuran and indole derivatives.","RSC advances","2024","14","37","27141","27152","10.1039/d4ra03485f","","","0.71073","MoKα","","0.0498","0.043","","","0.0883","0.0906","","","","","","1.206","","","","has coordinates","294268","2024-08-29","01:10:41","" "7249243","16.017","0.003","14.142","0.003","26.803","0.006","90","","90.347","0.009","90","","6071","2","297","2","297","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C54 H28 Fe2 N10 O22 -","- C54 H28 Fe2 N10 O22 -","- C216 H112 Fe8 N40 O88 -","4","0.5","","Sendh, Jagajiban; Baruah, Jubaraj B.","Bi-component sensing platform for the detection of Cd2+, Fe2+and Fe3+ ions.","RSC advances","2024","14","37","27153","27161","10.1039/d4ra04655b","","","0.71073","MoKα","","0.0532","0.0404","","","0.1122","0.1258","","","","","","1.045","","","","has coordinates","294269","2024-08-29","01:11:11","" "7249244","7.808","0.006","14.712","0.011","14.844","0.012","117.038","0.016","92.27","0.02","98.607","0.015","1490","2","298","2","298","2","","","","","","","","5","P -1","-P 1","2","","","","- C32 H20 Fe N5 O12 -","- C32 H20 Fe N5 O12 -","- C64 H40 Fe2 N10 O24 -","2","1","","Sendh, Jagajiban; Baruah, Jubaraj B.","Bi-component sensing platform for the detection of Cd2+, Fe2+and Fe3+ ions.","RSC advances","2024","14","37","27153","27161","10.1039/d4ra04655b","","","0.71073","MoKα","","0.0415","0.0375","","","0.1037","0.1062","","","","","","1.067","","","","has coordinates","294269","2024-08-29","01:11:11","" "7249245","10.9599","0.0003","10.3802","0.0004","14.7603","0.0004","90","","92.621","0.003","90","","1677.46","0.09","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","Nifedipine","dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate","","- C17 H18 N2 O6 -","- C17 H18 N2 O6 -","- C68 H72 N8 O24 -","4","1","","Singh, Vishal; Rajput, Khushbu; Singh, Sundaram; Srivastava, Vandana","Montmorillonite K-10 catalyzed synthesis of Hantzsch dihydropyridine derivatives from methyl arenes via in situ generated ammonia under microwave irradiation in neat conditions.","RSC advances","2024","14","37","27086","27091","10.1039/d4ra04990j","","x-ray","1.54184","CuKα","","0.1041","0.0873","","","0.2781","0.2991","","","","","","1.106","","","","has coordinates","294270","2024-08-29","01:11:27","" "7249246","18.7156","0.0007","8.5123","0.0003","21.5158","0.0009","90","","90","","90","","3427.7","0.2","180","","180","","","","","","","","","5","P b c a","-P 2ac 2ab","61","","6,6-difluoro-4-(4-methoxyphenyl)-5-(p-tolyl)-2-(trifluoromethyl)-6H-1,3-oxazine","","- C19 H14 F5 N O2 -","- C19 H14 F5 N O2 -","- C152 H112 F40 N8 O16 -","8","1","","Janecký, Lukáš; Klepetářová, Blanka; Beier, Petr","Transformation of 5-acylated N-fluoroalkyl-1,2,3-triazoles to trifluoromethylated ring-fused isoquinolines, 1,3-oxazines, and 1,3-oxazin-6-ones via ketenimines.","RSC advances","2024","14","37","26938","26942","10.1039/d4ra04794j","","x-ray","1.54178","CuKα","","0.0452","0.0398","","0.1099","0.1033","0.1098","","","","","","0.9901","","","","has coordinates","294271","2024-08-29","01:12:04","" "7249247","4.8502","0.0002","10.1006","0.0003","14.4402","0.0005","109.303","0.0012","97.3122","0.0013","95.91","0.0013","654.23","0.04","180","","180","","","","","","","","","5","P -1","-P 1","2","","2-fluoro-8-methoxy-2-methyl-5-(trifluoromethyl)-2,3-dihydro-1H-cyclopenta[c]isoquinolin-1-one","","- C15 H11 F4 N O2 -","- C15 H11 F4 N O2 -","- C30 H22 F8 N2 O4 -","2","1","","Janecký, Lukáš; Klepetářová, Blanka; Beier, Petr","Transformation of 5-acylated N-fluoroalkyl-1,2,3-triazoles to trifluoromethylated ring-fused isoquinolines, 1,3-oxazines, and 1,3-oxazin-6-ones via ketenimines.","RSC advances","2024","14","37","26938","26942","10.1039/d4ra04794j","","x-ray","1.54178","CuKα","","0.0355","0.0335","","0.0963","0.0929","0.0963","","","","","","0.978","","","","has coordinates","294271","2024-08-29","01:12:04","" "7249248","11.2617","0.0004","14.3039","0.0005","9.125","0.0003","90","","109.16","0.0011","90","","1388.48","0.08","180","","180","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","5-phenyl-4-(thiophen-2-yl)-2-(trifluoromethyl)-6H-1,3-oxazin-6-one","","- C15 H8 F3 N O2 S -","- C15 H8 F3 N O2 S -","- C60 H32 F12 N4 O8 S4 -","4","1","","Janecký, Lukáš; Klepetářová, Blanka; Beier, Petr","Transformation of 5-acylated N-fluoroalkyl-1,2,3-triazoles to trifluoromethylated ring-fused isoquinolines, 1,3-oxazines, and 1,3-oxazin-6-ones via ketenimines.","RSC advances","2024","14","37","26938","26942","10.1039/d4ra04794j","","x-ray","1.54178","CuKα","","0.0298","0.0284","","0.0738","0.0719","0.0738","","","","","","0.9336","","","","has coordinates,has disorder","294271","2024-08-29","01:12:04","" "7249272","13.8767","0.0004","13.7096","0.0004","26.8754","0.0008","90","","103.797","0.003","90","","4965.4","0.3","299","2","299","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C28 H16 Cd N2 O12 -","- C28 H16 Cd N2 O12 -","- C224 H128 Cd8 N16 O96 -","8","1","","Hou, Yaxin; Liu, Yang; Chai, Juan","A Cd-based MOF: iodine capture and enhanced efficiency of perovskite solar cells","RSC Advances","2024","14","38","27697","27702","10.1039/D4RA05219F","","x-ray","0.71073","MoKα","","0.0505","0.0378","","","0.0969","0.1033","","","","","","1.062","","","","has coordinates","294335","2024-09-03","01:17:51","" "7249273","22.162","0.003","7.1809","0.001","10.8505","0.0015","90","","90","","90","","1726.8","0.4","100.01","0.1","100.01","0.1","","","","","","","","5","P b c n","-P 2n 2ab","60","","","","- C7 H8 N2 O3 S -","- C7 H8 N2 O3 S -","- C56 H64 N16 O24 S8 -","8","1","","Pate, Sophie; Taujanskas, Joshua; Wells, Robyn; Robertson, Craig M.; O'Neill, Paul M.; Stachulski, Andrew V.","Convenient syntheses of 2-acylamino-4-halothiazoles and acylated derivatives using a versatile Boc-intermediate","RSC Advances","2024","14","38","27894","27903","10.1039/D4RA04959D","","x-ray","0.71073","MoKα","","0.0349","0.0306","","","0.0833","0.0867","","","","","","1.064","","","","has coordinates","294336","2024-09-03","01:18:20","" "7249274","5.0499","0.0002","7.4591","0.0003","9.4964","0.0003","90.462","0.003","91.106","0.003","108.081","0.004","339.94","0.02","100.01","0.1","100.01","0.1","","","","","","","","6","P -1","-P 1","2","","","","- C5 H5 Cl N2 O S -","- C5 H5 Cl N2 O S -","- C10 H10 Cl2 N4 O2 S2 -","2","1","","Pate, Sophie; Taujanskas, Joshua; Wells, Robyn; Robertson, Craig M.; O'Neill, Paul M.; Stachulski, Andrew V.","Convenient syntheses of 2-acylamino-4-halothiazoles and acylated derivatives using a versatile Boc-intermediate","RSC Advances","2024","14","38","27894","27903","10.1039/D4RA04959D","","x-ray","0.71073","MoKα","","0.0264","0.0251","","","0.0691","0.0701","","","","","","1.067","","","","has coordinates","294336","2024-09-03","01:18:20","" "7249275","20.4035","0.0006","8.6054","0.0003","23.5849","0.0006","90","","90","","90","","4141","0.2","150","","150","","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C42 H30 Cl2 N4 O12 S2 -","- C42 H30 Cl2 N4 O12 S2 -","- C168 H120 Cl8 N16 O48 S8 -","4","1","","Pate, Sophie; Taujanskas, Joshua; Wells, Robyn; Robertson, Craig M.; O'Neill, Paul M.; Stachulski, Andrew V.","Convenient syntheses of 2-acylamino-4-halothiazoles and acylated derivatives using a versatile Boc-intermediate","RSC Advances","2024","14","38","27894","27903","10.1039/D4RA04959D","","","0.71073","MoKα","","0.0584","0.0441","","","0.0999","0.1082","","","","","","1.038","","","","has coordinates","294336","2024-09-03","01:18:20","" "7249276","7.6951","0.0003","8.025","0.0002","11.2161","0.0006","83.335","0.003","76.981","0.004","81.112","0.003","664.34","0.05","303","2","303","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H11 Co N5 O4 -","- C14 H11 Co N5 O4 -","- C28 H22 Co2 N10 O8 -","2","1","","Mei, Zhen-Zhong; Wang, Hong-Yu; Ren, Chao; Yang, Ying; Gu, Jin-Zhong","Hydrothermal synthesis, structures, and catalytic performance of five coordination compounds driven by 5-aminoisophthalic acid","RSC Advances","2024","14","38","28160","28167","10.1039/D4RA05352D","","","0.71073","MoKα","","0.0406","0.0369","","","0.0759","0.0772","","","","","","1.136","","","","has coordinates","294354","2024-09-04","01:18:05","" "7249277","7.8965","0.0001","8.168","0.0001","11.425","0.0002","83.743","0.001","77.408","0.002","81.266","0.001","708.63","0.018","285","2","285","2","","","","","","","","5","P -1","-P 1","2","","","","- C14 H11 Cd N5 O4 -","- C14 H11 Cd N5 O4 -","- C28 H22 Cd2 N10 O8 -","2","1","","Mei, Zhen-Zhong; Wang, Hong-Yu; Ren, Chao; Yang, Ying; Gu, Jin-Zhong","Hydrothermal synthesis, structures, and catalytic performance of five coordination compounds driven by 5-aminoisophthalic acid","RSC Advances","2024","14","38","28160","28167","10.1039/D4RA05352D","","","1.54184","CuKα","","0.0237","0.0226","","","0.0579","0.0584","","","","","","1.037","","","","has coordinates","294354","2024-09-04","01:18:05","" "7249278","11.9238","0.0003","8.0959","0.0002","18.3412","0.0005","90","","95.998","0.002","90","","1760.85","0.08","303","2","303","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C28 H38 N10 Ni2 O16 -","- C28 H38 N10 Ni2 O16 -","- C56 H76 N20 Ni4 O32 -","2","0.5","","Mei, Zhen-Zhong; Wang, Hong-Yu; Ren, Chao; Yang, Ying; Gu, Jin-Zhong","Hydrothermal synthesis, structures, and catalytic performance of five coordination compounds driven by 5-aminoisophthalic acid","RSC Advances","2024","14","38","28160","28167","10.1039/D4RA05352D","","","0.71073","MoKα","","0.0384","0.0324","","","0.0864","0.0922","","","","","","1.031","","","","has coordinates","294354","2024-09-04","01:18:05","" "7249279","11.0968","0.0004","22.3594","0.0007","11.6156","0.0004","90","","107.065","0.004","90","","2755.15","0.17","293","2","293","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C32 H25 N4 Ni O5 -","- C32 H25 N4 Ni O5 -","- C128 H100 N16 Ni4 O20 -","4","1","","Mei, Zhen-Zhong; Wang, Hong-Yu; Ren, Chao; Yang, Ying; Gu, Jin-Zhong","Hydrothermal synthesis, structures, and catalytic performance of five coordination compounds driven by 5-aminoisophthalic acid","RSC Advances","2024","14","38","28160","28167","10.1039/D4RA05352D","","","0.71073","MoKα","","0.0364","0.03","","","0.0788","0.0826","","","","","","1.051","","","","has coordinates","294354","2024-09-04","01:18:06","" "7249280","10.1262","0.0003","13.2389","0.0003","13.3575","0.0003","88.8838","0.0017","75.6606","0.0019","74.27","0.002","1667.76","0.08","303","2","303","2","","","","","","","","5","P 1","P 1","1","","","","- C60 H55 N9 Ni3 O14 -","- C60 H55 N9 Ni3 O14 -","- C60 H55 N9 Ni3 O14 -","1","1","","Mei, Zhen-Zhong; Wang, Hong-Yu; Ren, Chao; Yang, Ying; Gu, Jin-Zhong","Hydrothermal synthesis, structures, and catalytic performance of five coordination compounds driven by 5-aminoisophthalic acid","RSC Advances","2024","14","38","28160","28167","10.1039/D4RA05352D","","","1.54184","CuKα","","0.0438","0.042","","","0.1184","0.1205","","","","","","1.066","","","","has coordinates","294354","2024-09-04","01:18:07","" "7249281","9.5063","0.0002","16.1542","0.0006","19.9926","0.0007","90","","95.61","0.003","90","","3055.49","0.17","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C27 H35 Br2 Co N5 O2 -","- C27 H35 Br2 Co N5 O2 -","- C108 H140 Br8 Co4 N20 O8 -","4","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.0754","0.0538","","","0.1438","0.1588","","","","","","1.037","","","","has coordinates","294355","2024-09-04","01:19:11","" "7249282","9.4553","0.0003","9.5655","0.0003","18.0521","0.0005","84.509","0.002","85.684","0.002","69.475","0.003","1520.53","0.09","99.98","0.13","100.15","","","","","","","","","6","P -1","-P 1","2","","","","- C29 H35 Co N7 O2 S2 -","- C29 H35 Co N7 O2 S2 -","- C58 H70 Co2 N14 O4 S4 -","2","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.0697","0.0624","","","0.1597","0.1647","","","","","","1.03","","","","has coordinates,has disorder","294355","2024-09-04","01:19:12","" "7249283","9.8084","0.0002","16.5786","0.0003","20.3177","0.0003","90","","92.489","0.002","90","","3300.73","0.1","293","2","293","2","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C27 H35 Cl0.51 Co I1.49 N5 O4.05 -","- C27 H35 Cl0.513 Co I1.487 N5 O4.052 -","- C108 H140 Cl2.052 Co4 I5.948 N20 O16.208 -","4","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.0561","0.0473","","","0.1282","0.1341","","","","","","1.032","","","","has coordinates,has disorder","294355","2024-09-04","01:19:12","" "7249284","10.1831","0.0003","15.8178","0.0004","19.919","0.0006","90","","93.777","0.003","90","","3201.47","0.16","100","0.1","100","0.1","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C28 H35 Cl Co N6 O7 -","- C28 H35 Cl Co N6 O7 -","- C112 H140 Cl4 Co4 N24 O28 -","4","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.071","0.0567","","","0.1553","0.1634","","","","","","1.077","","","","has coordinates,has disorder","294355","2024-09-04","01:19:12","" "7249285","10.2781","0.0004","15.7954","0.0004","19.6987","0.0005","90","","95.297","0.003","90","","3184.36","0.17","100","0.13","100","0.13","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C27 H35 Cl Co N8 O6 -","- C27 H35 Cl Co N8 O6 -","- C108 H140 Cl4 Co4 N32 O24 -","4","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.0881","0.0639","","","0.1708","0.1869","","","","","","1.033","","","","has coordinates,has disorder","294355","2024-09-04","01:19:12","" "7249286","9.2098","0.0001","32.9484","0.0003","9.7803","0.0001","90","","90","","90","","2967.81","0.05","100","","100","","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C29 H35 Co N7 O2 S2 -","- C29 H35 Co N7 O2 S2 -","- C116 H140 Co4 N28 O8 S8 -","4","1","","Zahradníková, Eva; Pichon, Céline; Duhayon, Carine; Sutter, Jean-Pascal; Halaš, Petr; Drahoš, Bohuslav","Synthesis, structural and magnetic properties of cobalt(ii) complexes with pyridine-based macrocyclic ligand containing two pyridine pendant arms","RSC Advances","2024","14","38","28138","28147","10.1039/D4RA02387K","","","1.54184","CuKα","","0.0274","0.0268","","0.0733","0.073","0.0733","","","","","","0.9526","","","","has coordinates","294355","2024-09-04","01:19:13","" "7249332","10.1982","0.0003","15.7867","0.0006","35.274","0.0011","87.532","0.003","83.977","0.003","72.535","0.003","5386.9","0.3","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C57 H72 Cl2 Fe N5 O7 -","- C57 H72 Cl2 Fe N5 O7 -","- C228 H288 Cl8 Fe4 N20 O28 -","4","2","","Poungsripong, Peeranuch; Boonprab, Theerapoom; Harding, Phimphaka; Murray, Keith S.; Phonsri, Wasinee; Zhang, Ningjin; Kitchen, Jonathan A.; Harding, David J.","Synthesis, mixed-spin-state structure and Langmuir-Blodgett deposition of amphiphilic Fe(iii) quinolylsalicylaldiminate complexes.","RSC advances","2024","14","39","28716","28723","10.1039/d4ra06111j","","x-ray","0.71073","MoKα","K-L~3~","0.1346","0.072","","","0.1572","0.1923","","","","","","1.025","","","","has coordinates","294728","2024-09-12","01:06:19","" "7249333","11.284","0.0004","12.1389","0.0004","19.1724","0.0005","87.836","0.002","79.244","0.002","74.869","0.003","2490.4","0.14","100","0.1","100","0.1","","","","","","","","4","P -1","-P 1","2","","","","- C28 H37 N2 O2.5 -","- C28 H37 N2 O2.5 -","- C112 H148 N8 O10 -","4","2","","Poungsripong, Peeranuch; Boonprab, Theerapoom; Harding, Phimphaka; Murray, Keith S.; Phonsri, Wasinee; Zhang, Ningjin; Kitchen, Jonathan A.; Harding, David J.","Synthesis, mixed-spin-state structure and Langmuir-Blodgett deposition of amphiphilic Fe(iii) quinolylsalicylaldiminate complexes.","RSC advances","2024","14","39","28716","28723","10.1039/d4ra06111j","","x-ray","0.71073","MoKα","","0.1076","0.0568","","","0.1323","0.158","","","","","","1.017","","","","has coordinates,has disorder","294728","2024-09-12","01:06:21","" "7249352","4.4615","0.0001","15.3156","0.0003","13.0669","0.0003","90","","97.558","0.002","90","","885.11","0.03","115","2","115","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C14 H20 N8 O6 -","- C14 H20 N8 O6 -","- C28 H40 N16 O12 -","2","1","","Konovalova, Irina S.; Shishkina, Svitlana V.; Wyshusek, Maik; Patzer, Michael; Reiss, Guido J.","Supramolecular architecture of theophylline polymorphs, monohydrate and co-crystals with iodine: study from the energetic viewpoint","RSC Advances","2024","14","41","29774","29788","10.1039/D4RA04368E","","","0.71073","MoKα","","0.0551","0.0407","","","0.0859","0.0926","","","","","","1.009","","","","has coordinates","294793","2024-09-19","01:15:52","" "7249353","3.8744","0.0004","12.8898","0.0009","8.1167","0.0006","90","","98.965","0.008","90","","400.4","0.06","290","2","293","2","","","","","","","","4","P 1 n 1","P -2yac","7","","","","- C7 H8 N4 O2 -","- C7 H8 N4 O2 -","- C14 H16 N8 O4 -","2","1","","Konovalova, Irina S.; Shishkina, Svitlana V.; Wyshusek, Maik; Patzer, Michael; Reiss, Guido J.","Supramolecular architecture of theophylline polymorphs, monohydrate and co-crystals with iodine: study from the energetic viewpoint","RSC Advances","2024","14","41","29774","29788","10.1039/D4RA04368E","","","0.71073","MoKα","","0.0689","0.0491","","","0.0908","0.0983","","","","","","1.033","","","","has coordinates","294793","2024-09-19","01:15:54","" "7249354","6.0794","0.0001","16.9054","0.0003","9.2013","0.0002","90","","99.973","0.002","90","","931.37","0.03","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C7 H8 I N4 O2 -","- C7 H8 I N4 O2 -","- C28 H32 I4 N16 O8 -","4","1","","Konovalova, Irina S.; Shishkina, Svitlana V.; Wyshusek, Maik; Patzer, Michael; Reiss, Guido J.","Supramolecular architecture of theophylline polymorphs, monohydrate and co-crystals with iodine: study from the energetic viewpoint","RSC Advances","2024","14","41","29774","29788","10.1039/D4RA04368E","","x-ray","0.71073","MoKα","","0.0194","0.0182","","","0.0482","0.0489","","","","","","1.069","","","","has coordinates","294793","2024-09-19","01:15:56","" "7249355","4.1492","0.0001","19.9564","0.0005","9.7232","0.0003","90","","90","","90","","805.11","0.04","135.15","","135.15","","","","","","","","","4","P b c m","-P 2c 2b","57","","5-(4-bromophenyl)-2H-tetrazole","","- C7 H5 Br N4 -","- C3.5 H2.5 Br0.5 N2 -","- C28 H20 Br4 N16 -","8","1","","Maurya, Anand; Patel, Upendra Kumar; Kumar, Sanjeev; Agarwal, Alka","Molybdenum trioxide as a newer diversified economic catalyst for the transformation of nitroarenes to arylamine and 5-substituted-1H-tetrazole","RSC Advances","2024","14","40","29505","29517","10.1039/D4RA05443A","","","1.54184","CuKα","","0.0441","0.0393","","","0.1207","0.1254","","","","","","1.088","","","","has coordinates","294794","2024-09-19","01:16:26","" "7249357","13.9608","0.0013","27.9958","0.0019","14.7493","0.0011","90","","116.436","0.011","90","","5161.9","0.9","298","2","298.15","","","","","","","","","5","C 1 c 1","C -2yc","9","","","","- C8 H58 O53 S4 Zr6 -","- C8 H32 O40 S4 Zr6 -","- C32 H128 O160 S16 Zr24 -","4","1","","Garzón-Serrano, Andrea Y.; Lozano, Johan D.; Perez, Leon D.; Sierra, César A.; Macías, Mario A.","Zr6O8 core cluster with formula unit [Zr6O4(OH)4(OH2)8(CH3COO)4(SO4)4]·nH2O obtained under mild conditions","RSC Advances","2024","14","41","29910","29918","10.1039/D4RA03940H","","","1.54184","CuKα","","0.0632","0.0517","","","0.1315","0.1437","","","","","","1.0233","","","","has coordinates","294817","2024-09-20","01:21:44","" "7249369","9.8359","0.0002","13.2198","0.0003","15.2566","0.0002","85.451","0.001","82.673","0.001","69.423","0.002","1840.79","0.07","100","0.13","100","0.13","","","","","","","","4","P -1","-P 1","2","","","","- C46 H50 N2 O2 -","- C46 H50 N2 O2 -","- C92 H100 N4 O4 -","2","1","","Dangar, Shilpa; Roy, Tiyasa; Noskar, Suman; Bisai, Alakesh","Total synthesis of bicyclomahanimbine by Cu(ii)-promoted photoredox process.","RSC advances","2024","14","41","30110","30115","10.1039/d4ra05863a","","x-ray","1.54184","CuKα","","0.048","0.0415","","","0.1112","0.1164","","","","","","1.057","","","","has coordinates","294877","2024-09-25","01:19:47","" "7249370","10.8951","0.0006","12.6583","0.0007","12.8328","0.0007","87.684","0.002","77.714","0.002","72.944","0.002","1652.77","0.16","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C28 H28 Cl2 N6 Ni O9 -","- C28 H28 Cl2 N6 Ni O9 -","- C56 H56 Cl4 N12 Ni2 O18 -","2","1","","Rajeev, Anjana; Muthuramalingam, Sethuraman; Sankaralingam, Muniyandi","Selective synthesis of cyclic alcohols from cycloalkanes using nickel(ii) complexes of tetradentate amidate ligands","RSC Advances","2024","14","41","30440","30451","10.1039/D4RA05222F","","","0.71073","MoKα","","0.0763","0.0708","","","0.2171","0.2247","","","","","","0.915","","","","has coordinates,has disorder","294878","2024-09-25","01:20:12","" "7249371","17.786","0.003","7.4291","0.0013","21.345","0.004","90","","101.411","0.005","90","","2764.6","0.8","100","2","100","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C23 H27 Cl2 N5 Ni O10 -","- C23 H27 Cl2 N5 Ni O10 -","- C92 H108 Cl8 N20 Ni4 O40 -","4","1","","Rajeev, Anjana; Muthuramalingam, Sethuraman; Sankaralingam, Muniyandi","Selective synthesis of cyclic alcohols from cycloalkanes using nickel(ii) complexes of tetradentate amidate ligands","RSC Advances","2024","14","41","30440","30451","10.1039/D4RA05222F","","","0.71073","MoKα","","0.0633","0.0429","","","0.0942","0.1045","","","","","","1.034","","","","has coordinates,has disorder","294878","2024-09-25","01:20:13","" "7249393","14.9362","0.0003","14.9362","0.0003","8.0716","0.0003","90","","90","","120","","1559.45","0.07","100","","100","","","","","","","","","5","P -3","-P 3","147","","","","- C33 H31 B N9 Na -","- C33 H31 B N9 Na -","- C66 H62 B2 N18 Na2 -","2","0.333333","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.0603","0.0439","","","0.0983","0.1156","","","","","","1.099","","","","has coordinates,has disorder","294917","2024-09-27","01:26:49","" "7249394","17.1463","0.0005","17.1463","0.0005","17.0555","0.0007","90","","90","","120","","4342.5","0.3","100","","100","","","","","","","","","6","R 3 c :H","R 3 -2""c","161","","","","- C27 H25 B N9 Na S3 -","- C27 H25 B N9 Na S3 -","- C162 H150 B6 N54 Na6 S18 -","6","0.333333","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.0399","0.0343","","","0.0782","0.0852","","","","","","1.18","","","","has coordinates","294917","2024-09-27","01:26:51","" "7249395","11.7918","0.0006","23.2058","0.0013","5.2271","0.0003","90","","90","","90","","1430.33","0.14","100","","100","","","","","","","","","6","P n m a","-P 2ac 2n","62","","","","- C14 H12 B K N4 O2 -","- C14 H12 B K N4 O2 -","- C56 H48 B4 K4 N16 O8 -","4","0.5","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.0349","0.0313","","","0.0747","0.0786","","","","","","1.109","","","","has coordinates","294917","2024-09-27","01:26:52","" "7249396","17.4388","0.0008","17.4388","0.0008","16.8446","0.0007","90","","90","","120","","4436.3","0.3","100","","100","","","","","","","","","6","R 3 c :H","R 3 -2""c","161","","","","- C27 H25 B K N9 S3 -","- C27 H25 B K N9 S3 -","- C162 H150 B6 K6 N54 S18 -","6","0.333333","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.0605","0.0452","","","0.0962","0.1122","","","","","","1.267","","","","has coordinates","294917","2024-09-27","01:27:01","" "7249397","15.7237","0.001","10.8738","0.0007","20.0182","0.0011","90","","111.251","0.002","90","","3189.9","0.3","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C32 H28 B2 N12 Na2 -","- C32 H28 B2 N12 Na2 -","- C128 H112 B8 N48 Na8 -","4","0.5","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.0767","0.0571","","","0.1335","0.1616","","","","","","1.126","","","","has coordinates","294917","2024-09-27","01:27:03","" "7249398","10.5827","0.0005","21.2856","0.0011","14.616","0.0006","90","","104.567","0.002","90","","3186.6","0.3","100","","100","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C32 H28 B2 Li2 N12 -","- C32 H28 B2 Li2 N12 -","- C128 H112 B8 Li8 N48 -","4","0.5","","Thomas, Jarrod R.; Mifsud, Jonathan T.; Sulway, Scott A.","Optimised syntheses and purifications of 3-aryl/heterocyclic dihydrobis- and hydrotris-(pyrazolyl)borate ligands as their alkali salts","RSC Advances","2024","14","42","30713","30718","10.1039/D4RA05723F","","","0.71073","MoKα","","0.087","0.061","","","0.1429","0.1817","","","","","","1.157","","","","has coordinates,has disorder","294917","2024-09-27","01:27:03","" "7249399","9.851","0.005","10.127","0.005","16.933","0.005","90","0.005","90","0.005","90","0.005","1689.3","1.3","293","2","293","2","","","","","","","","3","P n a 21","P 2c -2n","33","","","","- C23 H18 N2 -","- C23 H18 N2 -","- C92 H72 N8 -","4","1","","Zhang, Hong; Jiang, Yunhe; Sun, Xiaoxue; Liang, Tianyu; Wang, Xiang; Li, Yang","A new synthesis of indolo[2,3-b]quinolines from 3-acetyl-N-alkyl-2-chloroindoles with 2-aminobenzophenone","RSC Advances","2024","14","42","30707","30712","10.1039/D4RA05176A","","","0.71069","MoKα","","0.0849","0.0663","","","0.1769","0.1923","","","","","","1.08","","","","has coordinates","294919","2024-09-27","01:27:47","" "7249400","8.5868","0.0004","13.6623","0.0006","31.998","0.0016","90","","90","","90","","3753.9","0.3","296","2","293","2","","","","","","","","4","P b c a","-P 2ac 2ab","61","","","","- C24 H19 Cl N2 -","- C24 H19 Cl N2 -","- C192 H152 Cl8 N16 -","8","1","","Zhang, Hong; Jiang, Yunhe; Sun, Xiaoxue; Liang, Tianyu; Wang, Xiang; Li, Yang","A new synthesis of indolo[2,3-b]quinolines from 3-acetyl-N-alkyl-2-chloroindoles with 2-aminobenzophenone","RSC Advances","2024","14","42","30707","30712","10.1039/D4RA05176A","","","0.71073","MoKα","","0.0963","0.0612","","","0.1475","0.165","","","","","","1.087","","","","has coordinates","294919","2024-09-27","01:27:49","" "7249404","19.806","0.008","4.4215","0.0009","16.055","0.003","90","","113.91","0.02","90","","1285.3","0.7","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C14 H9 F2 N O3 -","- C14 H9 F2 N O3 -","- C56 H36 F8 N4 O12 -","4","1","","Khorasani, Fereshteh; Ranjbar-Karimi, Reza; Mohammadiannejad, Kazem","Utilizing perhalopyridine-based alkynes as suitable precursors for the synthesis of novel poly(1,2,3-triazolyl)-substituted perhalopyridines","RSC Advances","2024","14","42","30873","30885","10.1039/D4RA05861E","","","0.71073","MoKα","","0.1076","0.0786","","","0.1597","0.1736","","","","","","1.168","","","","has coordinates","294938","2024-09-29","00:59:06","" "7249405","13.02","0.003","9.949","0.004","27.886","0.006","90","","93.46","0.03","90","","3605.7","1.8","293","2","293","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C15 H9 Br Cl4 N4 O -","- C15 H9 Br Cl4 N4 O -","- C120 H72 Br8 Cl32 N32 O8 -","8","1","","Khorasani, Fereshteh; Ranjbar-Karimi, Reza; Mohammadiannejad, Kazem","Utilizing perhalopyridine-based alkynes as suitable precursors for the synthesis of novel poly(1,2,3-triazolyl)-substituted perhalopyridines","RSC Advances","2024","14","42","30873","30885","10.1039/D4RA05861E","","","0.71073","MoKα","","0.1046","0.0771","","","0.2002","0.2207","","","","","","1.063","","","","has coordinates","294938","2024-09-29","00:59:08","" "7249406","21.5606","0.0009","4.5954","0.0002","25.0465","0.001","90","","110.368","0.001","90","","2326.44","0.17","273","2","273","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C20 H20 Br4 N2 O4 Zn -","- C20 H20 Br4 N2 O4 Zn -","- C80 H80 Br16 N8 O16 Zn4 -","4","0.5","","Gishan, Md; Middya, Puspendu; Drew, Michael G. B.; Frontera, Antonio; Chattopadhyay, Shouvik","Synthesis, structural characterization, and theoretical analysis of novel zinc(ii) schiff base complexes with halogen and hydrogen bonding interactions","RSC Advances","2024","14","42","30896","30911","10.1039/D4RA06217E","","","0.71073","MoKα","","0.0619","0.0449","","","0.1099","0.1341","","","","","","1.201","","","","has coordinates,has disorder","294939","2024-09-29","00:59:34","" "7249407","21.494","0.002","13.8469","0.0013","9.6418","0.0013","90","","90","","90","","2869.6","0.5","273","2","273","2","","","","","","","","5","A e a 2","A 2 -2ab","41","","","","- C26 H34 N2 O8 Zn -","- C26 H34 N2 O8 Zn -","- C104 H136 N8 O32 Zn4 -","4","0.5","","Gishan, Md; Middya, Puspendu; Drew, Michael G. B.; Frontera, Antonio; Chattopadhyay, Shouvik","Synthesis, structural characterization, and theoretical analysis of novel zinc(ii) schiff base complexes with halogen and hydrogen bonding interactions","RSC Advances","2024","14","42","30896","30911","10.1039/D4RA06217E","","","0.71073","MoKα","","0.0646","0.05","","","0.14","0.1548","","","","","","1.027","","","","has coordinates,has disorder","294939","2024-09-29","00:59:35","" "7249408","12.5138","0.0005","11.9667","0.0004","16.7858","0.0007","90","","108.173","0.001","90","","2388.27","0.16","273","2","273","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C22 H26 Br2 N2 O4 Zn -","- C22 H26 Br2 N2 O4 Zn -","- C88 H104 Br8 N8 O16 Zn4 -","4","1","","Gishan, Md; Middya, Puspendu; Drew, Michael G. B.; Frontera, Antonio; Chattopadhyay, Shouvik","Synthesis, structural characterization, and theoretical analysis of novel zinc(ii) schiff base complexes with halogen and hydrogen bonding interactions","RSC Advances","2024","14","42","30896","30911","10.1039/D4RA06217E","","","0.71073","MoKα","","0.0949","0.0682","","","0.1997","0.2263","","","","","","1.037","","","","has coordinates","294939","2024-09-29","00:59:36","" "7249415","8.552","0.002","9.056","0.004","9.909","0.003","68.308","0.01","71.722","0.013","79.828","0.013","675.5","0.4","150","2","150","2","","","","","","","","4","P -1","-P 1","2","","Borane-N-benzyl-1-cyclohexylmethanamine","","- C14 H24 B N -","- C14 H24 B N -","- C28 H48 B2 N2 -","2","1","","Snyder, Madison J.; Alawaed, Abdulkhaliq A.; Li, Chunge; Pacentine, Samantha; Hamann, Henry J.; Ramachandran, P. Veeraraghavan","TiF4-mediated, one-pot, reductive amination of carboxylic acids with borane-ammonia.","RSC advances","2024","14","42","31205","31209","10.1039/d4ra05888g","","","0.71073","MoKα","","0.0698","0.0467","","","0.1199","0.1336","","","","","","1.048","","","","has coordinates","294978","2024-10-02","01:16:39","" "7249416","8.6436","0.0005","18.9145","0.0012","8.3234","0.0005","90","","99.035","0.006","90","","1343.9","0.14","293","2","293","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C13 H17 N3 O2 -","- C13 H17 N3 O2 -","- C52 H68 N12 O8 -","4","1","","Ajormal, Fatemeh; Bikas, Rahman; Ghasemzadeh, Hossein; Noshiranzadeh, Nader; Kozakiewicz-Piekarz, Anna","Green and recyclable catalyst based on chitosan/CuFe2O4 nanocomposite hydrogel for one-step synthesis of 1,2,3-triazoles","RSC Advances","2024","14","43","31320","31331","10.1039/D4RA05626D","","","0.71073","MoKα","","0.1097","0.0602","","","0.1184","0.1442","","","","","","1.041","","","","has coordinates","294979","2024-10-02","01:16:59","" "7249429","12.3314","0.0002","13.5371","0.0002","17.361","0.0003","90","","102.929","0.001","90","","2824.62","0.08","100","0.1","100","0.1","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C30 H25 Br N4 O3 P Re -","- C30 H25 Br N4 O3 P Re -","- C120 H100 Br4 N16 O12 P4 Re4 -","4","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0337","0.0302","","","0.0719","0.0737","","","","","","1.138","","","","has coordinates,has disorder","295078","2024-10-06","00:20:28","" "7249430","16.4795","0.0002","12.8391","0.0002","16.5133","0.0003","90","","111.481","0.0018","90","","3251.22","0.1","100","0.1","100","0.1","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C31.84 H27.51 F3 Mn N4.84 O5.16 P S -","- C31.836 H27.508 F3 Mn N4.836 O5.164 P S -","- C127.344 H110.032 F12 Mn4 N19.344 O20.656 P4 S4 -","4","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0383","0.0347","","","0.0894","0.0922","","","","","","1.032","","","","has coordinates,has disorder","295078","2024-10-06","00:20:42","" "7249431","16.4795","0.0002","12.8391","0.0002","16.5133","0.0003","90","","111.481","0.0018","90","","3251.22","0.1","100","2","100","2","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C31.92 H27.77 F3 Mn N4.92 O5.08 P S -","- C31.924 H27.772 F3 Mn N4.924 O5.076 P S -","- C127.696 H111.088 F12 Mn4 N19.696 O20.304 P4 S4 -","4","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0262","0.0261","","","0.0693","0.0694","","","","","","1.052","","","","has coordinates,has disorder","295078","2024-10-06","00:20:44","" "7249432","16.6364","0.0003","12.9137","0.0002","16.678","0.0003","90","","111.962","0.002","90","","3323.04","0.11","100","0.1","100","0.1","","","","","","","","8","P 1 21/n 1","-P 2yn","14","","","","- C32 H28 F3 N5 O5 P Re S -","- C32 H28 F3 N5 O5 P Re S -","- C128 H112 F12 N20 O20 P4 Re4 S4 -","4","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0431","0.0345","","","0.0839","0.0897","","","","","","1.052","","","","has coordinates","295078","2024-10-06","00:20:44","" "7249433","11.99461","0.00014","14.01447","0.00015","19.186","0.0002","90","","96.0115","0.0011","90","","3207.39","0.06","100","0.1","100","0.1","","","","","","","","8","P 1 21/c 1","-P 2ybc","14","","","","- C31 H25 F3 Mn N4 O6 P S -","- C31 H25 F3 Mn N4 O6 P S -","- C124 H100 F12 Mn4 N16 O24 P4 S4 -","4","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0321","0.0293","","","0.0743","0.0762","","","","","","1.045","","","","has coordinates","295078","2024-10-06","00:20:46","" "7249434","9.3815","0.0003","12.9857","0.0004","13.075","0.0005","64.443","0.003","85.597","0.003","88.991","0.003","1432.56","0.09","99.9","0.3","99.9","0.3","","","","","","","","8","P -1","-P 1","2","","","","- C28 H25 F3 Mn0.5 N4 O4 P S -","- C28 H25 F3 Mn0.5 N4 O4 P S -","- C56 H50 F6 Mn N8 O8 P2 S2 -","2","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.034","0.0307","","","0.0785","0.0815","","","","","","1.042","","","","has coordinates","295078","2024-10-06","00:20:47","" "7249435","8.9587","0.0003","12.2629","0.0004","14.9571","0.0005","99.615","0.002","90.746","0.002","94.564","0.002","1614.38","0.09","100","0.1","100","0.1","","","","","","","","8","P -1","-P 1","2","","","","- C31 H25 F3 N4 O6 P Re S -","- C31 H25 F3 N4 O6 P Re S -","- C62 H50 F6 N8 O12 P2 Re2 S2 -","2","1","","Valdivieso, Jorge P.; Erickson, Alexander N.; Gardinier, James R.","Group 7 carbonyl complexes of a PNN-heteroscorpionate ligand","RSC Advances","2024","14","43","31502","31516","10.1039/D4RA05287K","","x-ray","1.54184","CuKα","","0.0384","0.0349","","","0.0856","0.0881","","","","","","1.034","","","","has coordinates","295078","2024-10-06","00:20:50","" "7249436","5.9259","0.0001","10.326","0.0003","17.558","0.0004","90","","96.5555","0.001","90","","1067.36","0.04","298","","298","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C18 H18 Cd N4 O4 S2 -","- C18 H18 Cd N4 O4 S2 -","- C36 H36 Cd2 N8 O8 S4 -","2","0.5","","Saleh, Dalia I.; Mahmoud, Samy F.; Etaiw, Safaa Eldin H.","Synergistic impact of nano-supramolecular coordination polymer based on cadmium, ethyl nicotinate and thiocyanate ligands as efficient catalyst to remove harmful elements from wastewater","RSC Advances","2024","14","43","31471","31485","10.1039/D4RA05068A","","","0.71073","MoKα","","0.0799","0.0343","","0.1082","0.0711","0.0711","","","","","","0.9894","","","","has coordinates","295079","2024-10-06","00:22:02","" "7249437","7.4858","0.0003","8.0027","0.0003","12.7743","0.0005","90","","90","","90","","765.27","0.05","121","2","121","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C2 H4 As F7 O3 -","- C2 H4 As F7 O3 -","- C8 H16 As4 F28 O12 -","4","1","","Virmani, Alan; Jessen, Christoph; Nitzer, Alexander; Kornath, Andreas J.","Deoxyfluorination with superacids – synthesis and characterization of protonated α-fluorohydroxyacetic acid","RSC Advances","2024","14","43","31517","31523","10.1039/D4RA05449K","","","0.71073","MoKα","","0.0416","0.032","","","0.0587","0.0631","","","","","","1.028","","","","has coordinates","295080","2024-10-06","00:22:47","" "7249438","10.4665","0.0007","10.8561","0.0008","16.2199","0.0011","86.643","0.003","76.578","0.002","61.751","0.002","1576.31","0.19","300","","300","","","","","","","","","5","P -1","-P 1","2","","","","- C25 H21 N3 O4 S -","- C12.5 H10.5 N1.5 O2 S0.5 -","- C50 H42 N6 O8 S2 -","4","2","","Roys, Krupa Elsa; Manju, S. L.; Siddiq, Mohamed; Sambandam, Anandan","Novel A-π-D-A organic dyes for better photovoltaic performance.","RSC advances","2024","14","40","29229","29241","10.1039/d4ra05341a","","","0.71073","MoKα","","0.1416","0.0906","","","0.3076","0.375","","","","","","1.2725","","","","has coordinates","295081","2024-10-06","00:24:17","" "7249439","15.433","0.0011","15.7491","0.0019","19.3229","0.0015","90","","91.05","0.003","90","","4695.8","0.8","193","","193","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C30 H42 F12 N12 P2 Pt3 S2 -","- C30 H42 F12 N12 P2 Pt3 S2 -","- C120 H168 F48 N48 P8 Pt12 S8 -","4","1","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0544","0.0513","","","0.1054","0.1073","","","","","","1.002","","","","has coordinates","295082","2024-10-06","00:27:04","" "7249440","12.4809","0.0002","14.6151","0.0005","15.7052","0.0001","77.649","0.018","66.585","0.013","77.483","0.017","2540.1","0.3","193","2","193","2","","","","","","","","8","P -1","-P 1","2","","","","- C30.5 H46 F12 N12 O1.5 P2 Pt3 S2 -","- C29 H40 F12 N12 P2 Pt3 S2 -","- C58 H80 F24 N24 P4 Pt6 S4 -","2","1","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0437","0.0384","","","0.0889","0.0938","","","","","","1.062","","","","has coordinates","295082","2024-10-06","00:27:18","" "7249441","10.2266","0.0003","13.017","0.0008","16.8232","0.0011","99.891","0.004","93.302","0.003","90.379","0.002","2202.2","0.2","193","2","193","2","","","","","","","","7","P -1","-P 1","2","","","","- C30.5 H40 F12 N12 P2 Pt3 S2 -","- C28 H38 F12 N12 P2 Pt3 S2 -","- C56 H76 F24 N24 P4 Pt6 S4 -","2","1","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0255","0.0248","","","0.0581","0.0585","","","","","","1.119","","","","has coordinates","295082","2024-10-06","00:27:22","" "7249442","12.3687","0.0011","12.3687","0.0011","27.8127","0.0018","90","","90","","90","","4254.9","0.6","193","2","193.35","","","","","","","","","8","I 41","I 4bw","80","","","","- C32 H45 F6 N11 P Pt2 Rh S2 -","- C26 H36 F6 N8 P Pt2 Rh S2 -","- C104 H144 F24 N32 P4 Pt8 Rh4 S8 -","4","0.5","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0555","0.0492","","","0.1122","0.1169","","","","","","1.0062","","","","has coordinates,has disorder","295082","2024-10-06","00:27:24","" "7249443","16.814","0.007","17.82","0.007","22.082","0.009","101.846","0.007","92.738","0.012","92.657","0.005","6457","5","193","","193","","","","","","","","","8","P -1","-P 1","2","","","","- C72 H102 Ag3 F42 N30 P7 Pt6 S4 -","- C72 H102 Ag3 F42 N30 P7 Pt6 S4 -","- C144 H204 Ag6 F84 N60 P14 Pt12 S8 -","2","1","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0766","0.0625","","","0.1521","0.1643","","","","","","1.016","","","","has coordinates","295082","2024-10-06","00:27:30","" "7249444","14.1996","0.0006","14.1996","0.0006","16.3484","0.0007","90","","90","","120","","2854.7","0.2","193","","193.35","","","","","","","","","7","P 63/m","-P 6c","176","","","","- C39 H57 F12 N15 P2 Pt3 S2 -","- C39 H57 F12 N15 P2 Pt3 S2 -","- C78 H114 F24 N30 P4 Pt6 S4 -","2","0.166667","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0329","0.0328","","","0.0737","0.0737","","","","","","1.0282","","","","has coordinates,has disorder","295082","2024-10-06","00:27:34","" "7249445","17.827","0.004","25.802","0.004","13.476","0.003","90","","128.641","0.005","90","","4841.6","1.7","193","2","193.35","","","","","","","","","8","C 1 m 1","C -2y","8","","","","- C79 H85 B2 Cl6 N8 Pt2 Rh S2 -","- C76 H79 B2 N8 Pt2 Rh S2 -","- C152 H158 B4 N16 Pt4 Rh2 S4 -","2","0.5","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0447","0.0399","","","0.0958","0.102","","","","","","0.8978","","","","has coordinates,has disorder","295082","2024-10-06","00:27:37","" "7249446","24.235","0.002","12.8335","0.0009","20.6397","0.0018","90","","112.905","0.002","90","","5913.2","0.8","193","2","193.35","","","","","","","","","9","P 1 21/c 1","-P 2ybc","14","","","","- C36.2 H53.8 Ag2 F13 N15.2 O5.8 P3.5 Pt3 S2 -","- C30.2 H44.8 Ag2 F13 N12.2 O5.8 P3.5 Pt3 S2 -","- C120.8 H179.2 Ag8 F52 N48.8 O23.2 P14 Pt12 S8 -","4","1","","Yabune, Natsuki; Nakajima, Hiroshi; Nishioka, Takanori","Restriction of reaction sites on metal-sulfide cores induced by steric repulsion of bis-N-heterocyclic carbene ligands in trinuclear complexes bearing triply bridging sulfide ligands.","RSC advances","2024","14","40","29355","29367","10.1039/d4ra01671h","","","0.71075","MoKα","","0.0763","0.0684","","","0.1236","0.1283","","","","","","1.039","","","","has coordinates,has disorder","295082","2024-10-06","00:27:39","" "7249447","10.3826","0.0006","16.2352","0.001","21.2335","0.0014","106.864","0.002","102.927","0.002","102.216","0.002","3188.4","0.3","301","2","301","","","","","","","","","5","P -1","-P 1","2","","","","- C66.9 H43.1 N5.3 O21.3 Zn4 -","- C66 H41 N5 O21 Zn4 -","- C132 H82 N10 O42 Zn8 -","2","1","","Sendh, Jagajiban; Baruah, Jubaraj B.","Sequential effects of two cations on the fluorescence emission of a coordination polymer with Zn4O core in node.","RSC advances","2024","14","43","31598","31606","10.1039/d4ra06309k","","","0.71073","MoKα","","0.0704","0.0479","","","0.1309","0.1583","","","","","","1.098","","","","has coordinates,has disorder","295376","2024-10-09","01:25:01","" "7249448","9.9899","0.0011","14.6866","0.0016","17.88","0.002","88.277","0.005","77.431","0.004","78.288","0.005","2506.9","0.5","100","2","100","2","","","","","","","","7","P -1","-P 1","2","","Bis-(triphenylphosphine)- ?3-2,4,6-tris-(2-pyridyl)-1,3,5-triazine silver (I) perchlorate ethanol mono solvate","","- C56 H48 Ag Cl N6 O5 P2 -","- C56 H48 Ag Cl N6 O5 P2 -","- C112 H96 Ag2 Cl2 N12 O10 P4 -","2","1","","Hassoon, Azza A.; Smith, Stacey J.; Harrison, Roger G.","Cadmium and silver complexes of a pyridine containing ligand: syntheses, structural studies, biological activity and docking studies","RSC Advances","2024","14","43","31850","31860","10.1039/D4RA05305B","","","1.54178","CuKα","","0.0342","0.0336","","","0.0864","0.087","","","","","","1.075","","","","has coordinates,has disorder","295377","2024-10-09","01:25:26","" "7249453","7.629","0.0001","7.6702","0.0001","14.1025","0.0004","94.2128","0.0019","99.531","0.002","98.0165","0.0016","801.93","0.03","95","","95","","","","","","","","","7","P -1","-P 1","2","","","","- C12 H18 Cl N2 O2 P S2 -","- C12 H18 Cl N2 O2 P S2 -","- C24 H36 Cl2 N4 O4 P2 S4 -","2","1","","Hosseinpoor, Saeed; Pourayoubi, Mehrdad; Zmeškalová, Eliška; Poupon, Morgane","Supramolecular motifs formed by CH3/Cl-substituted arene groups: evidence for structural differences in thiophosphoramides and similarities in their complexes","RSC Advances","2024","14","44","32206","32220","10.1039/D4RA05281A","","","1.54184","CuKα","","0.0258","0.0255","","0.0713","0.071","0.0713","","","","","","0.9743","","","","has coordinates","295471","2024-10-13","00:55:42","" "7249454","7.8502","0.0002","10.1868","0.0004","11.6914","0.0004","113.275","0.003","97.462","0.003","97.123","0.003","835.66","0.05","120","","120","","","","","","","","","8","P -1","-P 1","2","","","","- C12 H17 Cl N2 Ni0.5 O2 P S2 -","- C12 H17 Cl N2 Ni0.5 O2 P S2 -","- C24 H34 Cl2 N4 Ni O4 P2 S4 -","2","1","","Hosseinpoor, Saeed; Pourayoubi, Mehrdad; Zmeškalová, Eliška; Poupon, Morgane","Supramolecular motifs formed by CH3/Cl-substituted arene groups: evidence for structural differences in thiophosphoramides and similarities in their complexes","RSC Advances","2024","14","44","32206","32220","10.1039/D4RA05281A","","","1.54184","CuKα","","0.0534","0.0496","","0.1414","0.1338","0.1414","","","","","","1.0003","","","","has coordinates","295471","2024-10-13","00:55:43","" "7249455","8.2171","0.0003","9.9942","0.0004","11.1612","0.0004","113.611","0.003","93.655","0.003","92.926","0.003","835.21","0.06","120","","120","","","","","","","","","7","P -1","-P 1","2","","","","- C13 H20 N2 Ni0.5 O2 P S2 -","- C13 H20 N2 Ni0.5 O2 P S2 -","- C26 H40 N4 Ni O4 P2 S4 -","2","1","","Hosseinpoor, Saeed; Pourayoubi, Mehrdad; Zmeškalová, Eliška; Poupon, Morgane","Supramolecular motifs formed by CH3/Cl-substituted arene groups: evidence for structural differences in thiophosphoramides and similarities in their complexes","RSC Advances","2024","14","44","32206","32220","10.1039/D4RA05281A","","","1.5418","CuKα","","0.049","0.045","","0.1393","0.1332","0.1393","","","","","","0.9943","","","","has coordinates","295471","2024-10-13","00:55:43","" "7249456","5.8046","0.0002","10.7878","0.0002","13.3907","0.0003","81.0002","0.0018","83.334","0.002","89.276","0.002","822.58","0.04","120","","120","","","","","","","","","6","P -1","-P 1","2","","","","- C13 H21 N2 O2 P S2 -","- C13 H21 N2 O2 P S2 -","- C26 H42 N4 O4 P2 S4 -","2","1","","Hosseinpoor, Saeed; Pourayoubi, Mehrdad; Zmeškalová, Eliška; Poupon, Morgane","Supramolecular motifs formed by CH3/Cl-substituted arene groups: evidence for structural differences in thiophosphoramides and similarities in their complexes","RSC Advances","2024","14","44","32206","32220","10.1039/D4RA05281A","","","1.54184","CuKα","","0.0328","0.0308","","0.0965","0.0877","0.0965","","","","","","1.0378","","","","has coordinates","295471","2024-10-13","00:55:44","" "7249457","26.4492","0.001","16.7231","0.0006","5.3699","0.0002","90","","94.146","0.004","90","","2368.96","0.15","150","0.1","150","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H19 F3 N2 O2 -","- C33 H19 F3 N2 O2 -","- C132 H76 F12 N8 O8 -","4","1","","Chen, Meiling; Chen, Yuzhuo; Zhang, Ting; Zhang, Hua; Xiao, Zhiwen; Su, Zhongzhen; Wu, Yunan","Molecular design and functional outcomes of RTP and TADF traits in isomers","RSC Advances","2024","14","44","32221","32228","10.1039/D4RA05807K","","x-ray","1.54184","CuKα","","0.1138","0.0901","","","0.2456","0.267","","","","","","1.07","","","","has coordinates","295472","2024-10-13","00:56:07","" "7249458","9.9594","0.0003","7.892","0.0002","32.1717","0.0009","90","","93.018","0.002","90","","2525.18","0.12","273","2","273","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C33 H19 F3 N2 O2 -","- C33 H19 F3 N2 O2 -","- C132 H76 F12 N8 O8 -","4","1","","Chen, Meiling; Chen, Yuzhuo; Zhang, Ting; Zhang, Hua; Xiao, Zhiwen; Su, Zhongzhen; Wu, Yunan","Molecular design and functional outcomes of RTP and TADF traits in isomers","RSC Advances","2024","14","44","32221","32228","10.1039/D4RA05807K","","","1.54184","CuKα","","0.076","0.0628","","","0.1616","0.1715","","","","","","1.049","","","","has coordinates","295472","2024-10-13","00:56:08","" "7249459","14.1951","0.0003","10.5832","0.0002","17.5467","0.0003","90","","98.318","0.002","90","","2608.3","0.09","292.9","0.3","292.9","0.3","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C33 H19 F3 N2 O2 -","- C33 H19 F3 N2 O2 -","- C132 H76 F12 N8 O8 -","4","1","","Chen, Meiling; Chen, Yuzhuo; Zhang, Ting; Zhang, Hua; Xiao, Zhiwen; Su, Zhongzhen; Wu, Yunan","Molecular design and functional outcomes of RTP and TADF traits in isomers","RSC Advances","2024","14","44","32221","32228","10.1039/D4RA05807K","","x-ray","1.54184","CuKα","","0.0772","0.0643","","","0.1798","0.1967","","","","","","1.048","","","","has coordinates","295472","2024-10-13","00:56:08","" "7249461","17.648","0.003","30.273","0.005","22.438","0.004","90","","90","","90","","11988","4","100","","100","","","","","","","","","6","P c a 21","P 2c -2ac","29","","","","- C36 H18 Eu F18 N3 O6 -","- C36 H18 Eu F18 N3 O6 -","- C432 H216 Eu12 F216 N36 O72 -","12","3","","Al-Sharji, Houda; Ilmi, Rashid; Oliveira, Willyan F.; Al-Saadi, Balqees S.; Dutra, José D. L.; Abou-Zied, Osama K.; Raithby, Paul R.; Khan, Muhammad S.","Deciphering intersystem crossing and energy transfer mechanisms in a nonacoordinated ternary europium(iii) complex: a combined spectroscopic and theoretical study","RSC Advances","2024","14","44","32573","32582","10.1039/D4RA06727D","","","0.71073","MoKα","","0.1048","0.0954","","","0.2334","0.2444","","","","","","1.079","","","","has coordinates,has disorder","295500","2024-10-16","01:15:03","" "7249462","8.2136","0.0001","12.8837","0.0002","9.3506","0.0002","90","","97.325","0.001","90","","981.42","0.03","194","2","194","2","","","","","","","","3","P 1 21/c 1","-P 2ybc","14","","","","- C24 H22 N6 -","- C24 H22 N6 -","- C48 H44 N12 -","2","0.5","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0444","0.0405","","","0.1073","0.1116","","","","","","1.044","","","","has coordinates","295515","2024-10-17","01:09:36","" "7249463","7.9002","0.0008","11.6313","0.0012","14.4637","0.0014","90","","90.13","0.003","90","","1329.1","0.2","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H22 Cl4 N6 Zn2 -","- C24 H22 Cl4 N6 Zn2 -","- C48 H44 Cl8 N12 Zn4 -","2","0.5","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0892","0.0747","","","0.1247","0.1295","","","","","","1.161","","","","has coordinates","295515","2024-10-17","01:09:37","" "7249464","8.1556","0.0004","11.6931","0.0007","14.6784","0.0008","90","","90.389","0.002","90","","1399.76","0.13","173","2","173","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C24 H22 Br4 N6 Zn2 -","- C24 H22 Br4 N6 Zn2 -","- C48 H44 Br8 N12 Zn4 -","2","0.5","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0509","0.0338","","","0.0682","0.0787","","","","","","1.131","","","","has coordinates","295515","2024-10-17","01:09:37","" "7249465","7.9366","0.0006","19.2414","0.0016","11.2733","0.0009","90","","96.936","0.002","90","","1709","0.2","173","2","173","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C28 H38 Cl2 N6 O12 Zn -","- C28 H38 Cl2 N6 O12 Zn -","- C56 H76 Cl4 N12 O24 Zn2 -","2","0.5","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0421","0.036","","","0.0924","0.0981","","","","","","1.054","","","","has coordinates","295515","2024-10-17","01:09:38","" "7249466","14.9058","0.0003","10.4325","0.0002","20.5991","0.0004","90","","109.478","0.001","90","","3019.93","0.1","193","2","193","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C24 H22 I4 N6 Zn2 -","- C24 H22 I4 N6 Zn2 -","- C96 H88 I16 N24 Zn8 -","4","1","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0419","0.034","","","0.0705","0.0739","","","","","","1.031","","","","has coordinates","295515","2024-10-17","01:09:38","" "7249467","10.9854","0.0009","12.5818","0.0011","25.124","0.002","81.71","0.002","80.594","0.003","75.975","0.002","3303.8","0.5","173","2","173","2","","","","","","","","6","P -1","-P 1","2","","","","- C54 H68 Cl4 N12 O22 Zn2 -","- C54 H68 Cl4 N12 O22.003 Zn2 -","- C108 H136 Cl8 N24 O44.006 Zn4 -","2","1","","Kwon, So Hyeon; Lee, Sunwoo; Tessarolo, Jacopo; Lee, Haeri","Stimuli-responsive Zn(ii) complexes showing the structural conversion and on/off switching of catalytic properties","RSC Advances","2024","14","44","32655","32660","10.1039/D4RA06058J","","","0.71073","MoKα","","0.0933","0.057","","","0.116","0.1334","","","","","","1.074","","","","has coordinates,has disorder","295515","2024-10-17","01:09:38","" "7249481","12.2065","0.0013","15.7058","0.0016","14.4096","0.0015","90","","104.927","0.004","90","","2669.3","0.5","300","2","300","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C32 H46 N16 O20 U4 -","- C32 H46 N16 O20 U4 -","- C64 H92 N32 O40 U8 -","2","0.5","","S., Nakul; R., Bhagavathish; Kulkarni, Naveen V.; Patil, Ajeetkumar; Arakera, Suresh B.; John, Sam","Synthesis and characterization of novel uranyl clusters supported by bis(pyrazolyl) methane ligands: biomimetic catalytic oxidation, BSA protein interaction and cytotoxicity studies","RSC Advances","2024","14","45","32802","32817","10.1039/D4RA06347C","","","0.71073","MoKα","","0.087","0.0509","","","0.0934","0.1048","","","","","","1.054","","","","has coordinates","295562","2024-10-20","01:16:32","" "7249482","8.4881","0.0017","9.075","0.0018","14.96","0.003","93.295","0.006","105.306","0.006","92.251","0.006","1107.9","0.4","298","2","298","","","","","","","","","6","P -1","-P 1","2","","","","- C42 H24 Cu I2 N8 O6 -","- C42 H24 Cu I2 N8 O6 -","- C42 H24 Cu I2 N8 O6 -","1","0.5","","Paul, Eshani; Raza, Rameez; Dhara, Subrata Ranjan; Baildya, Nabajyoti; Ghosh, Kumaresh","6-Aminocoumarin-derived Schiff base gelators: aggregation and sensing of CN−, Fe3+, Cu2+ and CO2 under different conditions","RSC Advances","2024","14","45","32759","32770","10.1039/D4RA05503A","","","0.71073","MoKα","","0.1975","0.1089","","","0.1656","0.1987","","","","","","1.062","","","","has coordinates","295563","2024-10-20","01:16:44","" "7249490","10.137","0.002","11.456","0.003","13.238","0.003","113.447","0.009","91.736","0.01","95.668","0.01","1399.4","0.6","273.15","","273.15","","","","","","","","","4","P -1","-P 1","2","","RN_BP_BDS110","","- C36 H29 Cl2 N3 -","- C35 H27 N3 -","- C70 H54 N6 -","2","1","","Das, Barnali; Bhattacharyya, Arghyadeep; Paul, Bhaswati; Natarajan, Ramalingam; Majumdar, Swapan","An elegant approach for the synthesis of multisubstituted imidazole via FeCl3/SiO2 catalyzed activation of acetals: a photophysical study of an imidazole-carbazole hybrid.","RSC advances","2024","14","45","33512","33523","10.1039/d4ra06436d","","x-ray","1.54178","CuKα","","0.0692","0.0649","","","0.2066","0.212","","","","","","1.033","","","","has coordinates","295602","2024-10-24","01:01:28","" "7249516","7.7958","0.0004","6.4753","0.0003","22.4577","0.0012","90","","90.521","0.002","90","","1133.62","0.1","273.15","","273.15","","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C8 H9 Br Cl N5 O2 -","- C8 H9 Br Cl N5 O2 -","- C32 H36 Br4 Cl4 N20 O8 -","4","1","","Naskar, Shibu; Mal, Susital; Shivangi, Shivangi; Das, Subrata","A rapid and scalable method for visible light induced bromination of uracil derivatives in a falling film looping photoreactor","RSC Advances","2024","14","47","34925","34937","10.1039/D4RA05774K","","","0.71073","MoKα","","0.0381","0.0376","","","0.1051","0.1056","","","","","","1.156","","","","has coordinates","295725","2024-11-02","02:03:46","" "7249517","4.6708","0.0005","15.134","0.001","13.5776","0.0008","90","","92.765","0.007","90","","958.65","0.13","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C7 H8 Br Cl N2 O2 -","- C7 H8 Br Cl N2 O2 -","- C28 H32 Br4 Cl4 N8 O8 -","4","1","","Naskar, Shibu; Mal, Susital; Shivangi, Shivangi; Das, Subrata","A rapid and scalable method for visible light induced bromination of uracil derivatives in a falling film looping photoreactor","RSC Advances","2024","14","47","34925","34937","10.1039/D4RA05774K","","x-ray","0.71073","MoKα","","0.0787","0.047","","","0.0944","0.1076","","","","","","1.004","","","","has coordinates","295725","2024-11-02","02:03:47","" "7249518","10.9173","0.0007","8.5748","0.0004","8.1733","0.0005","90","","109.345","0.007","90","","721.93","0.08","293","2","293","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C5 H4 Br Cl N2 O2 -","- C5 H4 Br Cl N2 O2 -","- C20 H16 Br4 Cl4 N8 O8 -","4","1","","Naskar, Shibu; Mal, Susital; Shivangi, Shivangi; Das, Subrata","A rapid and scalable method for visible light induced bromination of uracil derivatives in a falling film looping photoreactor","RSC Advances","2024","14","47","34925","34937","10.1039/D4RA05774K","","x-ray","0.71073","MoKα","","0.0427","0.0416","","","0.1014","0.1034","","","","","","1.096","","","","has coordinates","295725","2024-11-02","02:03:47","" "7249536","4.7062","0.0004","23.5001","0.0018","6.3164","0.0005","90","","107.641","0.001","90","","665.72","0.09","296","2","296","2","","","","","","","","5","P 1 21 1","P 2yb","4","","2-Benzylsulfinyl-1-methyl-1H-benzo[d]imidazole","","- C15 H14 N2 O S -","- C15 H14 N2 O S -","- C30 H28 N4 O2 S2 -","2","1","","Capozzi, Maria Annunziata M.; Alvarez-Larena, Angel; Piniella Febrer, Joan F.; Cardellicchio, Cosimo","Investigation of the titanium-mediated catalytic enantioselective oxidation of aryl benzyl sulfides containing heterocyclic groups","RSC Advances","2024","14","47","35105","35113","10.1039/D4RA07088G","","","0.71073","MoKα","","0.0481","0.0446","","","0.1116","0.1142","","","","","","1.094","","","","has coordinates","295771","2024-11-05","02:06:41","" "7249537","8.188","0.0004","7.0323","0.0004","12.3527","0.0007","90","","102.82","0.03","90","","693.54","0.11","296","2","296","2","","","","","","","","6","P 1 21 1","P 2yb","4","","(2,3,4,5,6-pentafluorobenzylsulfinyl)-1H-benzo[d]imidazole","","- C14 H7 F5 N2 O S -","- C14 H7 F5 N2 O S -","- C28 H14 F10 N4 O2 S2 -","2","1","","Capozzi, Maria Annunziata M.; Alvarez-Larena, Angel; Piniella Febrer, Joan F.; Cardellicchio, Cosimo","Investigation of the titanium-mediated catalytic enantioselective oxidation of aryl benzyl sulfides containing heterocyclic groups","RSC Advances","2024","14","47","35105","35113","10.1039/D4RA07088G","","","0.71073","MoKα","","0.0361","0.0351","","","0.0965","0.0976","","","","","","1.056","","","","has coordinates","295771","2024-11-05","02:06:53","" "7249538","5.4947","0.0011","9.2154","0.0018","23.473","0.005","90","","90","","90","","1188.6","0.4","296","2","296","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","2-(2,3,4,5,6-pentafluorobenzylsulfinyl)thiophene","","- C11 H5 F5 O S2 -","- C11 H5 F5 O S2 -","- C44 H20 F20 O4 S8 -","4","1","","Capozzi, Maria Annunziata M.; Alvarez-Larena, Angel; Piniella Febrer, Joan F.; Cardellicchio, Cosimo","Investigation of the titanium-mediated catalytic enantioselective oxidation of aryl benzyl sulfides containing heterocyclic groups","RSC Advances","2024","14","47","35105","35113","10.1039/D4RA07088G","","","0.71073","MoKα","","0.042","0.0407","","","0.1218","0.1236","","","","","","1.078","","","","has coordinates","295771","2024-11-05","02:06:56","" "7249539","13.2625","0.001","13.2625","0.001","12.4674","0.001","90","","90","","120","","1899.1","0.3","296","2","296","2","","","","","","","","5","P 64","P 64","172","","Benzylsulfinyl-1H-benzo[d]imidazole","","- C14 H12 N2 O S -","- C14 H12 N2 O S -","- C84 H72 N12 O6 S6 -","6","1","","Capozzi, Maria Annunziata M.; Alvarez-Larena, Angel; Piniella Febrer, Joan F.; Cardellicchio, Cosimo","Investigation of the titanium-mediated catalytic enantioselective oxidation of aryl benzyl sulfides containing heterocyclic groups","RSC Advances","2024","14","47","35105","35113","10.1039/D4RA07088G","","","0.71073","MoKα","","0.1141","0.0659","","","0.0907","0.1026","","","","","","1.096","","","","has coordinates","295771","2024-11-05","02:06:57","" "7249551","17.9401","0.0007","11.5274","0.0005","18.6602","0.0007","90","","109.066","0.0012","90","","3647.3","0.3","150","2","150","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C34 H36 N2 O15 Tb2 -","- C34 H36 N2 O15 Tb2 -","- C136 H144 N8 O60 Tb8 -","4","0.5","","Liu, Ching-Ping; Lin, Ting-En; Chiang, Jung-Chang; Chen, Bo-Jhen; Chien, Po-Hsiu; Chien, Su-Ying; Lee, Gene-Hsiang; Liu, Yen-Hsiang; Lu, Kuang-Lieh","An exceptional water stable terbium-based metal–organic framework for selective detection of pesticides","RSC Advances","2024","14","47","35220","35226","10.1039/D4RA06622G","","","0.71073","MoKα","","0.0347","0.0307","","","0.0711","0.0738","","","","","","1.279","","","","has coordinates,has disorder","295790","2024-11-06","02:16:59","" "7249558","13.395","0.003","13.251","0.003","9.036","0.002","90","","98.213","0.004","90","","1587.4","0.6","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C16 H14 Cl2 O2 Te -","- C16 H14 Cl2 O2 Te -","- C64 H56 Cl8 O8 Te4 -","4","1","","Singh, Puspendra; Khan, Mariya; Duthie, Andrew; Butcher, Ray J.","Synthesis and characterization of carbonyl functionalized organotellurium(iv) derivatives","RSC Advances","2024","14","48","35650","35656","10.1039/D4RA06023G","","","0.71073","MoKα","","0.0255","0.0224","","","0.057","0.0586","","","","","","1.04","","","","has coordinates","295849","2024-11-09","02:04:17","" "7249559","8.389","0.005","12.312","0.005","8.461","0.005","90","0.005","116.32","0.005","90","0.005","783.3","0.7","100","2","100","2","","","","","","","","5","P 1 21 1","P 2yb","4","","","","- C14 H18 Cl2 O2 Te -","- C14 H18 Cl2 O2 Te -","- C28 H36 Cl4 O4 Te2 -","2","1","","Singh, Puspendra; Khan, Mariya; Duthie, Andrew; Butcher, Ray J.","Synthesis and characterization of carbonyl functionalized organotellurium(iv) derivatives","RSC Advances","2024","14","48","35650","35656","10.1039/D4RA06023G","","","0.71073","MoKα","","0.0344","0.0292","","","0.0569","0.0601","","","","","","1.019","","","","has coordinates","295849","2024-11-09","02:04:18","" "7249560","8.7845","0.0004","19.5434","0.0008","11.0751","0.0005","90","","97.679","0.004","90","","1884.31","0.14","123","2","123","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C19 H20 Cl2 O2 Te -","- C19 H20 Cl2 O2 Te -","- C76 H80 Cl8 O8 Te4 -","4","1","","Singh, Puspendra; Khan, Mariya; Duthie, Andrew; Butcher, Ray J.","Synthesis and characterization of carbonyl functionalized organotellurium(iv) derivatives","RSC Advances","2024","14","48","35650","35656","10.1039/D4RA06023G","","","0.71073","MoKα","","0.0515","0.0345","","","0.0652","0.0707","","","","","","1.088","","","","has coordinates","295849","2024-11-09","02:04:18","" "7249561","19.262","0.003","4.9631","0.0009","30.819","0.005","90","","98.509","0.003","90","","2913.8","0.8","296","2","296.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C22.67 H18.67 N2.67 O1.33 S1.33 -","- C22.6667 H18.6667 N2.66667 O1.33333 S1.33333 -","- C136 H112 N16 O8 S8 -","6","0.75","","Aggarwal, Ranjana; Sharma, Shilpa; Jain, Naman; Sanz, Dionisia; Claramunt, Rosa M.; Delgado, Patricia; Torralba, M. Carmen","Reaction of unsymmetrical α-bromo-1,3-diketones with N-substituted thioureas: regioselective access to 2-(N-arylamino)-5-acyl-4-methylthiazoles and/or rearranged 2-(N-acylimino)-3-N-aryl-4-methylthiazoles","RSC Advances","2024","14","48","35585","35600","10.1039/D4RA05436A","","","0.71073","MoKα","","0.1173","0.058","","","0.1336","0.1535","","","","","","0.967","","","","has coordinates,has disorder","295850","2024-11-09","02:04:51","" "7249562","9.4627","0.001","9.6608","0.001","11.0027","0.0011","107.81","0.002","110.578","0.002","96.95","0.002","866.57","0.16","296.15","","296.15","","","","","","","","","6","P -1","-P 1","2","","","","- C18 H15 Cl N2 O2 S -","- C18 H15 Cl N2 O2 S -","- C36 H30 Cl2 N4 O4 S2 -","2","1","","Aggarwal, Ranjana; Sharma, Shilpa; Jain, Naman; Sanz, Dionisia; Claramunt, Rosa M.; Delgado, Patricia; Torralba, M. Carmen","Reaction of unsymmetrical α-bromo-1,3-diketones with N-substituted thioureas: regioselective access to 2-(N-arylamino)-5-acyl-4-methylthiazoles and/or rearranged 2-(N-acylimino)-3-N-aryl-4-methylthiazoles","RSC Advances","2024","14","48","35585","35600","10.1039/D4RA05436A","","","0.71073","MoKα","","0.0994","0.048","","","0.1115","0.1292","","","","","","0.97","","","","has coordinates","295850","2024-11-09","02:04:53","" "7249563","20.1281","0.0015","6.9154","0.0005","11.345","0.0009","90","","90","","90","","1579.2","0.2","296","2","296.15","","","","","","","","","5","P n m a","-P 2ac 2n","62","","","","- C18 H16 N2 O S -","- C18 H16 N2 O S -","- C72 H64 N8 O4 S4 -","4","0.5","","Aggarwal, Ranjana; Sharma, Shilpa; Jain, Naman; Sanz, Dionisia; Claramunt, Rosa M.; Delgado, Patricia; Torralba, M. Carmen","Reaction of unsymmetrical α-bromo-1,3-diketones with N-substituted thioureas: regioselective access to 2-(N-arylamino)-5-acyl-4-methylthiazoles and/or rearranged 2-(N-acylimino)-3-N-aryl-4-methylthiazoles","RSC Advances","2024","14","48","35585","35600","10.1039/D4RA05436A","","","0.71073","MoKα","","0.088","0.0441","","","0.1198","0.1377","","","","","","1.004","","","","has coordinates,has disorder","295850","2024-11-09","02:04:53","" "7249591","14.7703","0.0005","9.2488","0.0003","26.0606","0.0008","90","","90","","90","","3560.1","0.2","101","2","101","2","","","","","","","","6","P n a 21","P 2c -2n","33","","","","- C28 H30 Cl4 Cu2 N10 S4 -","- C28 H30 Cl4 Cu2 N10 S4 -","- C112 H120 Cl16 Cu8 N40 S16 -","4","1","","Rogalewicz, B.; Sierański, T; Szczesio, M.; Olczak, A.; Gobis, K.; Orlewska, C.; Korona-Głowniak, I; Korga-Plewko, A; Iwan, M.; Michalczuk, M.; Kubik, J.; Adamczuk, G.; Korga, M.; Rutkowska, N.; Boruta, T.; Gas, K.; Sawicki, M.; Poleszak, E.; Maniukiewicz, W.; Świątkowski, M; Czylkowska, A.","Physicochemical properties and mechanism of action of a new copper(ii) pyrazine-based complex with high anticancer activity and selectivity towards cancer cells.","RSC advances","2024","14","49","36295","36307","10.1039/d4ra06874b","","x-ray","0.71073","MoKα","","0.0551","0.0475","","","0.1005","0.1026","","","","","","1.039","","","","has coordinates","295913","2024-11-14","02:16:11","" "7249592","6.9582","0.0003","7.7761","0.0004","34.9263","0.0015","88.781","0.004","89.088","0.003","89.979","0.004","1889.11","0.15","295","2","295","2","","","","","","","","2","P -1","-P 1","2","","","","- C46 H62 -","- C46 H62 -","- C92 H124 -","2","1","","Yang, Tengzhou; Zhang, Liang; Bao, Yucong; Wei, Haoming","Dialkylated dibenzo[a,h]anthracenes for solution-processable organic thin-film transistors","RSC Advances","2024","14","49","36390","36397","10.1039/D4RA07439D","","x-ray","1.54184","CuKα","","0.1679","0.1174","","","0.3056","0.3415","","","","","","1.088","","","","has coordinates","295926","2024-11-15","02:06:31","" "7249593","25.7538","0.0005","5.7788","0.0001","25.3638","0.0004","90","","112.982","0.002","90","","3475.18","0.12","289","1","289","1","","","","","","","","2","C 1 2/c 1","-C 2yc","15","","","","- C44 H54 -","- C44 H54 -","- C176 H216 -","4","0.5","","Yang, Tengzhou; Zhang, Liang; Bao, Yucong; Wei, Haoming","Dialkylated dibenzo[a,h]anthracenes for solution-processable organic thin-film transistors","RSC Advances","2024","14","49","36390","36397","10.1039/D4RA07439D","","x-ray","1.54184","CuKα","","0.0863","0.0782","","","0.2576","0.2708","","","","","","1.132","","","","has coordinates","295926","2024-11-15","02:06:31","" "7249594","25.8074","0.0013","4.65278","0.00014","26.1585","0.0013","90","","116.535","0.006","90","","2810.1","0.3","99.97","0.15","99.97","0.15","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C15 H12 F3 N3 O3 -","- C15 H12 F3 N3 O3 -","- C120 H96 F24 N24 O24 -","8","2","","Hu, Ming-Cheng; Zhou, Hai-Tao; Fang, Yu-Chen; Zhang, Li-Ren; Cui, Bao-Dong; Chen, Yong-Zheng; Bai, Mei","In situ generated CF3CHN2 with 3-ylideneoxindoles to access CF3-containing pyrazolo[1,5-c]quinazolines derivatives","RSC Advances","2024","14","49","36410","36415","10.1039/D4RA06651K","","x-ray","1.54184","CuKα","","0.1181","0.1144","","","0.3068","0.3085","","","","","","1.108","","","","has coordinates","295927","2024-11-15","02:06:54","" "7249598","13.4291","0.0006","4.1088","0.0002","16.6768","0.0007","90","","90","","90","","920.18","0.07","173","","173","","","","","","","","","4","P n a 21","P 2c -2n","33","","","","- C11 H7 Br N2 -","- C11 H7 Br N2 -","- C44 H28 Br4 N8 -","4","1","","Li, Yingqian; Liu, Yali; Hao, Di; Xu, Liang; Liu, Ping","Regioselective bromination of pyrrolo[1,2-a]quinoxalines","RSC Advances","2024","14","49","36488","36496","10.1039/D4RA07358D","","","1.54178","CuKα","","0.0309","0.028","","","0.0635","0.0659","","","","","","1.053","","","","has coordinates","295960","2024-11-16","02:08:09","" "7249600","10.7755","0.0006","26.7963","0.0015","12.0718","0.0006","90","","102.178","0.003","90","","3407.2","0.3","150","","150","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","(E)-N-(6-chloro-2-phenylimidazo[1,2-a]pyridin-3-yl)-1-(4-nitrophenyl)methanimine","","- C20 H13 Cl N4 O2 -","- C20 H13 Cl N4 O2 -","- C160 H104 Cl8 N32 O16 -","8","2","","Azzouzi, Mohamed; Ouchaoui, Abderrahim Ait; Azougagh, Omar; El Hadad, Salah Eddine; Abou-salama, Mohamed; Oussaid, Adyl; Pannecouque, Christophe; Rohand, Taoufik","Synthesis, crystal structure, and antiviral evaluation of new imidazopyridine-schiff base derivatives: in vitro and in silico anti-HIV studies","RSC Advances","2024","14","50","36902","36918","10.1039/D4RA07561G","","x-ray","1.34139","GaKα","","0.0508","0.0407","","","0.1019","0.1088","","","","","","1.064","","","","has coordinates","296002","2024-11-20","02:01:23","" "7249626","9.7936","0.0009","9.8228","0.0008","16.0752","0.0014","95.357","0.003","96.286","0.004","107.679","0.003","1451.4","0.2","296","2","296","2","","","","","","","","3","P -1","-P 1","2","","","","- C34 H30 O7 -","- C34 H30 O7 -","- C68 H60 O14 -","2","1","","Ponraj, Pravinkamaraj; Rajendran, Saravanakumar","Design and synthesis of a novel curcumin–combretastatin A4 molecular skeleton: two pharmacophores","RSC Advances","2024","14","50","37227","37233","10.1039/D4RA06618A","","","0.71073","MoKα","","0.1024","0.0504","","","0.1154","0.1493","","","","","","1.046","","","","has coordinates,has disorder","296040","2024-11-21","02:27:39",""