# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2025-01-13T22:34:19+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 'ACS Sustainable Chemistry & Engineering') AND volume = 9 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
"4518408","17.095","0.0003","14.339","0.0002","38.364","0.0006","90","","106.233","0.001","90","","9029.1","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C164 H312 N16 O19 Zn8 -","- C164 H312 N16 O19 Zn8 -","- C328 H624 N32 O38 Zn16 -","2","0.5","","Krupiński, Piotr; Grala, Agnieszka; Wolska-Pietkiewicz, Małgorzata; Danowski, Wojciech; Justyniak, Iwona; Lewiński, Janusz","From Uncommon Ethylzinc Complexes Supported by Ureate Ligands to Water-Soluble ZnO Nanocrystals: A Mechanochemical Approach","ACS Sustainable Chemistry & Engineering","2021","9","4","1540","1549","10.1021/acssuschemeng.0c06081","","","0.71073","MoKα","","0.0754","0.0579","","","0.1435","0.1523","","","","","","1.033","","","","has coordinates,has disorder","261497","2021-02-04","03:29:47",""
"4518484","7.272","0.002","11.453","0.004","12.792","0.004","105.317","0.011","97.72","0.011","94.62","0.01","1010.7","0.6","304","2","304","2","","","","","","","","5","P -1","-P 1","2","","","","- C26 H45 N8 O30 Zn3.5 -","- C26 H45 N8 O30 Zn3.5 -","- C26 H45 N8 O30 Zn3.5 -","1","0.5","","Li, Yixing; Zhang, Xiao; Lan, Jianwen; Li, Dazhi; Wang, Zhijiang; Xu, Ping; Sun, Jianmin","A High-Performance Zinc-Organic Framework with Accessible Open Metal Sites Catalyzes CO2 and Styrene Oxide into Styrene Carbonate under Mild Conditions","ACS Sustainable Chemistry & Engineering","2021","9","7","2795","2803","10.1021/acssuschemeng.0c08466","","","0.71073","MoKα","","0.0636","0.0625","","","0.1759","0.1765","","","","","","1.068","","","","has coordinates,has disorder","262444","2021-03-04","02:53:01",""
"4518547","7.9105","0.0008","10.1433","0.0014","12.1778","0.0013","68.787","0.005","73.015","0.004","71.871","0.005","847.74","0.17","170","2","169.96","","","","","","","","","4","P -1","-P 1","2","","","","- C20 H27 N O2 -","- C20 H27 N O2 -","- C40 H54 N2 O4 -","2","1","","Zhou, Kun; Hao, Hong-Yan; Mao, Yang-Jie; Wu, Qiu-Zi; Chen, Lei; Wang, Shuang; Jin, Wu; Xu, Zhen-Yuan; Lou, Shao-Jie; Xu, Dan-Qian","Solvent-less Dehydrogenative C‒H Etherification with Alcohols Using Mechanochemistry","ACS Sustainable Chemistry & Engineering","2021","9","12","4433","4439","10.1021/acssuschemeng.0c08201","","","1.34139","GaKα","","0.0509","0.0452","","","0.1212","0.1275","","","","","","1.051","","","","has coordinates","263591","2021-04-04","10:00:09",""
"4518570","8.0272","0.0006","10.3866","0.0008","21.6398","0.0015","90","","95.314","0.003","90","","1796.5","0.2","295","2","295","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C14 H14 N4 O6 V2 Zn -","- C14 H14 N4 O6 V2 Zn -","- C56 H56 N16 O24 V8 Zn4 -","4","1","","Tian, Hongrui; Liu, Shumei; Zhang, Zhong; Dang, Tianyi; Lu, Ying; Liu, Shuxia","Highly Stable Polyoxovanadate-Based Zn‒MOF with Dual Active Sites as a Solvent-free Catalyst for C‒C Bond Formation","ACS Sustainable Chemistry & Engineering","2021","9","12","4660","4667","10.1021/acssuschemeng.1c00389","","","0.71073","MoKα","","0.0595","0.0351","","","0.0705","0.0793","","","","","","1.061","","","","has coordinates","263590","2021-04-04","10:00:02",""
"4518716","7.3124","0.0012","8.0674","0.0014","11.1844","0.0017","90.429","0.013","96.849","0.014","93.54","0.014","653.76","0.19","293","2","293","2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H8 Br N O2 S2 -","- C12 H8 Br N O2 S2 -","- C24 H16 Br2 N2 O4 S4 -","2","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.1533","0.0859","","","0.2208","0.2932","","","","","","1.013","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518717","7.5012","0.0013","7.6684","0.0014","12.37","0.002","77.306","0.015","82.115","0.015","74.588","0.015","666.8","0.2","299.5","0.2","299.5","0.2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H8 Br N O2 S2 -","- C12 H8 Br N O2 S2 -","- C24 H16 Br2 N2 O4 S4 -","2","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0651","0.0473","","","0.105","0.1169","","","","","","1.145","","","","has coordinates,has disorder","265752","2021-06-04","00:58:59",""
"4518718","7.4862","0.0008","7.6173","0.0007","12.26","0.0009","77.313","0.007","81.768","0.008","74.085","0.009","653.34","0.11","299.8","0.2","299.8","0.2","","","","","","","","6","P -1","-P 1","2","","","","- C12 H8 Cl N O2 S2 -","- C12 H8 Cl N O2 S2 -","- C24 H16 Cl2 N2 O4 S4 -","2","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0433","0.0393","","","0.1005","0.1035","","","","","","1.078","","","","has coordinates,has disorder","265752","2021-06-04","00:58:59",""
"4518719","6.637","0.0005","24.4347","0.0018","7.9539","0.0009","90","","93.577","0.008","90","","1287.4","0.2","299.4","0.4","299.4","0.4","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H11 N O2 S2 -","- C13 H11 N O2 S2 -","- C52 H44 N4 O8 S8 -","4","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0538","0.0352","","","0.0663","0.0749","","","","","","1.102","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518720","5.4415","0.0011","7.9266","0.0009","30.427","0.005","90","","94.695","0.019","90","","1308","0.4","299.1","0.3","299.1","0.3","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H9 Cl O2 S2 -","- C13 H9 Cl O2 S2 -","- C52 H36 Cl4 O8 S8 -","4","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.1121","0.0966","","","0.2322","0.2589","","","","","","1.061","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518721","5.4811","0.0003","7.9282","0.0003","30.7236","0.0013","90","","95.134","0.005","90","","1329.75","0.11","293","2","293","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C13 H9 Br O2 S2 -","- C13 H9 Br O2 S2 -","- C52 H36 Br4 O8 S8 -","4","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0499","0.0443","","","0.1248","0.1304","","","","","","1.09","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518722","5.9037","0.0002","12.98","0.0004","17.9041","0.0006","90","","90","","90","","1371.99","0.08","299.4","0.3","299.4","0.3","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C14 H14 O2 S2 -","- C14 H14 O2 S2 -","- C56 H56 O8 S8 -","4","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0292","0.0281","","","0.0744","0.0757","","","","","","1.037","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518723","5.7416","0.0003","13.0516","0.001","14.497","0.0008","90","","90","","90","","1086.36","0.12","100","0.2","100","0.2","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C12 H8 F2 S2 -","- C12 H8 F2 S2 -","- C48 H32 F8 S8 -","4","1","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","1.54184","CuKα","","0.0779","0.0609","","","0.1362","0.1578","","","","","","1.193","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4518724","7.7242","0.0008","28.033","0.004","5.9565","0.0005","90","","90","","90","","1289.8","0.3","293","","293","","","","","","","","","4","C c c 2","C 2 -2c","37","","","","- C12 H8 Br2 S2 -","- C12 H8 Br2 S2 -","- C48 H32 Br8 S8 -","4","0.5","","Sobczak, Szymon; Ratajczyk, Paulina; Katrusiak, Andrzej","Squeezing Out the Catalysts: A Sustainable Approach to Disulfide Bond Exchange in Aryl Disulfides","ACS Sustainable Chemistry & Engineering","2021","9","20","7171","7178","10.1021/acssuschemeng.1c02240","","x-ray","0.71","MoKα","","0.093","0.0535","","","0.0993","0.1186","","","","","","0.983","","","","has coordinates","265752","2021-06-04","00:58:59",""
"4519018","8.6254","0.0003","8.9016","0.0003","10.8499","0.0003","80.225","0.003","85.954","0.003","77.248","0.003","800.24","0.05","120","2","120","2","","","","","","","","6","P -1","-P 1","2","","","","- C19 H15 F N O2 P -","- C19 H15 F N O2 P -","- C38 H30 F2 N2 O4 P2 -","2","1","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0297","0.0277","","","0.0699","0.0714","","","","","","1.038","","","","has coordinates","268443","2021-09-03","21:23:48",""
"4519019","11.1796","0.0004","12.4375","0.0006","14.5087","0.0007","102.974","0.004","93.417","0.004","104.758","0.004","1886.37","0.16","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C21 H20 N O4 P -","- C21 H20 N O4 P -","- C84 H80 N4 O16 P4 -","4","2","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0369","0.0318","","","0.0798","0.083","","","","","","1.01","","","","has coordinates","268443","2021-09-03","21:23:49",""
"4519020","8.7838","0.0004","8.7951","0.0004","20.4442","0.0008","90.45","0.003","93.891","0.003","117.301","0.004","1398.88","0.12","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C15 H16 N O2 P -","- C15 H16 N O2 P -","- C60 H64 N4 O8 P4 -","4","2","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0404","0.0356","","","0.1038","0.1059","","","","","","1.058","","","","has coordinates","268443","2021-09-03","21:23:49",""
"4519021","13.2516","0.0002","14.607","0.0002","17.427","0.0003","108.164","0.001","109.21","0.001","94.747","0.001","2961.45","0.09","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H18 N O2 P -","- C16 H18 N O2 P -","- C128 H144 N8 O16 P8 -","8","4","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0302","0.0281","","","0.0762","0.0779","","","","","","1.034","","","","has coordinates,has disorder","268443","2021-09-03","21:23:49",""
"4519022","8.7408","0.0002","10.399","0.0003","11.263","0.0003","82.043","0.002","85.124","0.002","82.282","0.002","1002.41","0.05","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C47.01 H44.01 N2 O4 P2 -","- C47.014 H44.014 N2 O4 P2 -","- C47.014 H44.014 N2 O4 P2 -","1","0.5","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0366","0.0352","","","0.0898","0.0905","","","","","","1.049","","","","has coordinates,has disorder","268443","2021-09-03","21:23:50",""
"4519023","8.4872","0.0003","11.6741","0.0005","16.8354","0.0006","108.405","0.004","96.291","0.003","90.405","0.003","1571.67","0.11","120","2","120","2","","","","","","","","5","P -1","-P 1","2","","","","- C18 H16 N O3 P -","- C18 H16 N O3 P -","- C72 H64 N4 O12 P4 -","4","2","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.06","0.0388","","","0.0852","0.0953","","","","","","1.025","","","","has coordinates,has disorder","268443","2021-09-03","21:23:50",""
"4519024","12.1934","0.0001","10.7695","0.0001","13.8808","0.0001","90","","105.735","0.001","90","","1754.48","0.03","120","2","120","2","","","","","","","","7","P 1 21/n 1","-P 2yn","14","","","","- C19 H15 Cl N O P S -","- C19 H15 Cl N O P S -","- C76 H60 Cl4 N4 O4 P4 S4 -","4","1","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0287","0.0278","","","0.0725","0.0732","","","","","","1.06","","","","has coordinates","268443","2021-09-03","21:23:50",""
"4519025","12.1983","0.0001","10.781","0.0001","13.9142","0.0001","90","","104.72","0.001","90","","1769.8","0.03","120","2","120","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C20 H18 N O2 P S -","- C20 H18 N O2 P S -","- C80 H72 N4 O8 P4 S4 -","4","1","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0257","0.0254","","","0.0664","0.0666","","","","","","1.03","","","","has coordinates","268443","2021-09-03","21:23:50",""
"4519026","18.8671","0.0001","11.7269","0.0001","16.0554","0.0001","90","","95.579","0.001","90","","3535.47","0.04","120","2","120","2","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C19 H15 N2 O3 P S -","- C19 H15 N2 O3 P S -","- C152 H120 N16 O24 P8 S8 -","8","1","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.027","0.0269","","","0.0735","0.0736","","","","","","1.071","","","","has coordinates","268443","2021-09-03","21:23:50",""
"4519027","9.0779","0.0001","16.1069","0.0002","10.5344","0.0001","90","","102.06","0.001","90","","1506.31","0.03","120","2","120","2","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C16 H16 N O P S -","- C16 H16 N O P S -","- C64 H64 N4 O4 P4 S4 -","4","1","","Huke, Cameron D.; Taylor, Laurence J.; Argent, Stephen P.; Kays, Deborah L.","Catalyst-free Hydrophosphinylation of Isocyanates and Isothiocyanates under Low-Added-Solvent Conditions","ACS Sustainable Chemistry & Engineering","2021","9","32","10704","10709","10.1021/acssuschemeng.1c02907","","x-ray","1.54184","CuKα","","0.0257","0.0246","","","0.0638","0.0646","","","","","","1.052","","","","has coordinates","268443","2021-09-03","21:23:50",""
"4519080","17.223","0.004","8.252","0.002","15.149","0.004","90","","99.137","0.004","90","","2125.7","0.9","130","2","130","","","","","","","","","6","P 1 21/c 1","-P 2ybc","14","","","","- C18 H33 B F4 N2 O2 -","- C18 H33 B F4 N2 O2 -","- C72 H132 B4 F16 N8 O8 -","4","1","","del Río, Enrique; Vidil, Thomas; Gati, Wafa; Grau, Étienne; Taton, Daniel; Cramail, Henri","Ester-Containing Imidazolium-Type Ionic Liquid Crystals Derived from Bio-based Fatty Alcohols","ACS Sustainable Chemistry & Engineering","2021","9","37","12687","12698","10.1021/acssuschemeng.1c05122","","","1.54178","CuKα","","0.0824","0.0702","","","0.1801","0.189","","","","","","0.955","","","","has coordinates","269502","2021-10-03","21:17:00",""
"4519192","12.4443","0.001","12.4258","0.0011","18.7974","0.0017","90","","108.271","0.003","90","","2760.1","0.4","150","2","150","2","","","","","","","","7","P 1 2/c 1","-P 2yc","13","","","","- C40 H70 Mo24 N8 O96 P2 Zn8 -","- C40 H32 Mo24 N8 O96 P2 Zn8 -","- C40 H32 Mo24 N8 O96 P2 Zn8 -","1","0.25","","Chen, Yanhong; Chang, Shenzhen; An, Haiyan; Li, Yanqin; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui","Two Polymorphic Polyoxometalate-Based Metal–Organic Frameworks for the Efficient Synthesis of Functionalized Sulfoxides and Detoxification of Mustard Gas Simulants","ACS Sustainable Chemistry & Engineering","2021","9","46","15683","15693","10.1021/acssuschemeng.1c06433","","","0.71073","MoKα","","0.1033","0.0499","","","0.1009","0.1171","","","","","","1.011","","","","has coordinates","271058","2021-12-03","22:39:13",""
"4519193","12.398","0.003","12.41","0.003","18.721","0.004","90","","109.145","0.009","90","","2721.1","1.1","150","2","150","2","","","","","","","","7","P 1 2/n 1","-P 2yac","13","","","","- C40 H70 Mo24 N8 O96 P2 Zn8 -","- C40 H32 Mo24 N8 O96 P2 Zn8 -","- C40 H32 Mo24 N8 O96 P2 Zn8 -","1","0.25","","Chen, Yanhong; Chang, Shenzhen; An, Haiyan; Li, Yanqin; Zhu, Qingshan; Luo, Huiyun; Huang, Yaohui","Two Polymorphic Polyoxometalate-Based Metal–Organic Frameworks for the Efficient Synthesis of Functionalized Sulfoxides and Detoxification of Mustard Gas Simulants","ACS Sustainable Chemistry & Engineering","2021","9","46","15683","15693","10.1021/acssuschemeng.1c06433","","","0.71073","MoKα","","0.1049","0.0815","","","0.1907","0.1999","","","","","","1.071","","","","has coordinates","271058","2021-12-03","22:39:14",""
"4519267","31.3976","0.0009","6.9692","0.0002","19.2078","0.0005","90","","125.086","0.002","90","","3439.25","0.19","298","2","298","2","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C22 H15 Cl N2 O -","- C22 H15 Cl N2 O -","- C176 H120 Cl8 N16 O8 -","8","1","","Cai, Chen; Lu, Yi; Yuan, Chengcheng; Fang, Zheng; Yang, Xiaobing; Liu, Chengkou; Guo, Kai","Organocatalytic Electrosynthesis of Cinnolines through Cascade Radical Cyclization and Migration","ACS Sustainable Chemistry & Engineering","2021","9","50","16989","16996","10.1021/acssuschemeng.1c05810","","","1.54178","CuKα","","0.0655","0.0543","","","0.1459","0.1602","","","","","","1.007","","","","has coordinates","271762","2022-01-03","22:40:18",""
"4519268","11.1841","0.0005","11.7671","0.0004","12.2739","0.0006","90","","105.7","0.005","90","","1555.04","0.12","113.15","","113.15","","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C19 H20 F2 N2 O -","- C19 H20 F2 N2 O -","- C76 H80 F8 N8 O4 -","4","1","","Niu, Kaikai; Zhou, Pan; Ding, Ling; Hao, Yanke; Liu, Yuxiu; Song, Hongjian; Wang, Qingmin","Photoelectrochemical Decarboxylative C–H Alkylation of Quinoxalin-2(1H)-ones","ACS Sustainable Chemistry & Engineering","2021","9","49","16820","16828","10.1021/acssuschemeng.1c06702","","x-ray","0.71073","MoKα","","0.082","0.0533","","","0.1263","0.1501","","","","","","1.04","","","","has coordinates","271764","2022-01-03","22:40:42",""