# Search results of SQL query from the Crystallography Open Database
# Date and time performed: 2024-11-28T07:55:15+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 'Catalysis science & technology') 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
"1570094","17.915","0.0008","22.4618","0.0009","25.0531","0.0008","90","","90","","90","","10081.4","0.7","100","2","100","2","","","","","","","","7","P c c n","-P 2ab 2ac","56","","","","- C47.25 H43.5 Cl2.5 F10 Ir N4 O4 -","- C47.262 H43.527 Cl2.5 F10 Ir N4 O4 -","- C378.096 H348.216 Cl20 F80 Ir8 N32 O32 -","8","1","","Tan, Yi Zhen; Wu, Xiangyang; Lu, Yunpeng; Chiba, Shunsuke; Yeow, Edwin K. L.","Towards catalytic redox-active iridium polypyridyl complex by in situ photosubstitution","Catalysis Science & Technology","2024","14","1","66","75","10.1039/D3CY00942D","","x-ray","0.71073","MoKα","","0.0918","0.0477","","","0.1185","0.1493","","","","","","1.066","","","","has coordinates,has disorder","289310","2024-02-04","10:57:35",""
"1570095","25.7551","0.0005","19.7204","0.0004","22.789","0.0004","90","","90","","90","","11574.6","0.4","100","2","100","2","","","","","","","","6","P b c n","-P 2n 2ab","60","","","","- C53 H52 F10 Ir N5 O4 -","- C52.5 H52 F10 Ir N5 O4 -","- C420 H416 F80 Ir8 N40 O32 -","8","1","","Tan, Yi Zhen; Wu, Xiangyang; Lu, Yunpeng; Chiba, Shunsuke; Yeow, Edwin K. L.","Towards catalytic redox-active iridium polypyridyl complex by in situ photosubstitution","Catalysis Science & Technology","2024","14","1","66","75","10.1039/D3CY00942D","","x-ray","0.71073","MoKα","","0.1087","0.0851","","","0.23","0.2591","","","","","","1.115","","","","has coordinates,has disorder","289310","2024-02-04","10:57:36",""
"1570363","7.948","0.002","8.256","0.002","10.775","0.003","75.188","0.008","78.772","0.008","73.732","0.008","650.4","0.3","298","2","298","","","","","","","","","5","P -1","-P 1","2","","Cobaltbromide_Pyridine3_methylpyrazole","","- C10 H11 Br2 Co N3 -","- C10 H11 Br2 Co N3 -","- C20 H22 Br4 Co2 N6 -","2","1","","Kumar, Rohit; Srivastava, Ankit Kumar; Nagarasu, Palaniyappan; Madhu, Vedichi; Balaraman, Ekambaram","A general and expedient amination of alcohols catalysed by a single-site (NN)Co(ii)-bidentate complex under solventless conditions","Catalysis Science & Technology","2024","14","1","98","109","10.1039/D3CY00809F","","","0.71073","MoKα","","0.0249","0.024","","","0.0579","0.0588","","","","","","1.075","","","","has coordinates","289311","2024-02-04","10:57:44",""
"1570384","6.95","0.0004","9.8071","0.0006","11.6221","0.0005","90.667","0.004","105.074","0.004","107.794","0.005","724.72","0.07","100","0.1","100","0.1","","","","","","","","5","P -1","-P 1","2","","","","- C15 H12 F4 O3 S -","- C15 H12 F4 O3 S -","- C30 H24 F8 O6 S2 -","2","1","","Mathuri, Ashis; Pal, Buddhadeb; Pramanik, Milan; Manna, Anupam; Mal, Prasenjit","Enhancing the photocatalytic efficiency and stability of CsPbBr3 nanocrystals for visible-light driven aerobic diaryl thio/seleno etherification","Catalysis Science & Technology","2024","14","1","183","189","10.1039/D3CY01478A","","x-ray","0.71073","MoKα","","0.0356","0.0313","","","0.0803","0.0827","","","","","","0.992","","","","has coordinates","289312","2024-02-04","10:57:51",""
"1570453","6.10213","0.00005","7.30975","0.00006","29.70773","0.00019","92.3183","0.0006","93.944","0.0006","114.298","0.0008","1201.43","0.018","180","2","180","2","","","","","","","","4","P 1","P 1","1","","","","- C54 H74 N2 O8 -","- C54 H74 N2 O8 -","- C54 H74 N2 O8 -","1","1","","Zhang, Fan; Wang, Su-Jing; Xiao, Wen; Yu, Ming-Zhu; Sha, Feng; Wu, Ruibo; Xiang, Zheng","Harnessing the catalytic plasticity of the ent-kaurene synthase from Bradyrhizobium japonicum to produce the ent-rosane and ent-pimarane scaffolds","Catalysis Science & Technology","2024","14","2","306","314","10.1039/D3CY00115F","","","1.54184","CuKα","","0.0326","0.0322","","","0.0887","0.0891","","","","","","1.082","","","","has coordinates","289314","2024-02-04","10:58:31",""
"1570630","5.23281","0.00004","11.33461","0.00009","22.611","0.0002","90","","90","","90","","1341.1","0.019","150.01","0.1","150.01","0.1","","","","","","","","4","P 21 21 21","P 2ac 2ab","19","","","","- C16 H17 N O2 -","- C16 H17 N O2 -","- C64 H68 N4 O8 -","4","1","","Obieta, Maria; Urgoitia, Garazi; Herrero, María Teresa; SanMartin, Raul","Efficient iron-catalyzed direct acylation of amines with carboxylic acids and esters under oxygenated conditions","Catalysis Science & Technology","2024","14","2","478","488","10.1039/D3CY01429K","","x-ray","1.54184","CuKα","","0.0286","0.0281","","","0.0721","0.0725","","","","","","1.075","","","","has coordinates","289313","2024-02-04","10:58:23",""
"1570631","5.4042","0.0001","22.6075","0.0004","23.7568","0.0004","90","","95.144","0.002","90","","2890.81","0.09","170","0.1","170","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C17 H19 N O2 -","- C17 H19 N O2 -","- C136 H152 N8 O16 -","8","4","","Obieta, Maria; Urgoitia, Garazi; Herrero, María Teresa; SanMartin, Raul","Efficient iron-catalyzed direct acylation of amines with carboxylic acids and esters under oxygenated conditions","Catalysis Science & Technology","2024","14","2","478","488","10.1039/D3CY01429K","","x-ray","1.54184","CuKα","","0.0704","0.0601","","","0.1633","0.1738","","","","","","1.131","","","","has coordinates,has disorder","289313","2024-02-04","10:58:23",""
"1570946","13.2667","0.0011","13.8534","0.0012","22.0429","0.0019","90","","93.349","0.002","90","","4044.3","0.6","296.15","","296.15","","","","","","","","","5","C 1 2/c 1","-C 2yc","15","","","","- C40 H46 N6 O12 Zn -","- C40 H46 N6 O12 Zn -","- C160 H184 N24 O48 Zn4 -","4","0.5","","Khattak, Zafar A. K.; Ahmad, Nazir; Younus, Hussein A.; Ullah, Habib; Yu, Baoyi; Munawar, Khurram S.; Ashfaq, Muhammad; Yaseen, Muhammad; Danish, Muhammad; Al-Abri, Mohammed; AlHajri, Rashid; Verpoort, Francis","Ambient conversion of CO2 and epoxides to cyclic carbonates using 3D amide-functionalized MOFs","Catalysis Science & Technology","2024","14","7","1888","1901","10.1039/D3CY01709E","","","0.71073","MoKα","","0.0487","0.0382","","","0.1027","0.1092","","","","","","1.049","","","","has coordinates","290794","2024-04-04","22:21:04",""
"1570973","26.1891","0.0017","7.1383","0.0004","14.0543","0.0011","90","","120.864","0.004","90","","2255.3","0.3","210","","210","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","","","- C9 H5 Mn0.5 N4 O5 Pb -","- C9 H5 Mn0.5 N4 O5 Pb -","- C72 H40 Mn4 N32 O40 Pb8 -","8","1","","Wang, Xiyu; Yang, Guo-Ping; Wang, Yao-Yu","Catalytic comparison of cyanosilylation/Knoevenagel condensation reactions by Pb-based heterometallic organic frameworks with different second metal ions","Catalysis Science & Technology","2024","14","6","1613","1621","10.1039/D3CY01549A","","","0.71073","MoKα","","0.0226","0.0213","","","0.0563","0.0571","","","","","","1.142","","","","has coordinates","290793","2024-04-04","22:20:54",""
"1570974","26.201","0.006","7.1538","0.0017","14.084","0.004","90","","120.846","0.008","90","","2266.4","1","256","","256","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","PbZn","","- C9 H5 N4 O5 Pb Zn0.5 -","- C9 H5 N4 O5 Pb Zn0.5 -","- C72 H40 N32 O40 Pb8 Zn4 -","8","1","","Wang, Xiyu; Yang, Guo-Ping; Wang, Yao-Yu","Catalytic comparison of cyanosilylation/Knoevenagel condensation reactions by Pb-based heterometallic organic frameworks with different second metal ions","Catalysis Science & Technology","2024","14","6","1613","1621","10.1039/D3CY01549A","","","0.71073","MoKα","","0.026","0.0236","","","0.0548","0.0561","","","","","","1.11","","","","has coordinates","290793","2024-04-04","22:20:55",""
"1570975","26.2822","0.0012","7.2428","0.0002","14.042","0.0006","90","","120.511","0.001","90","","2302.86","0.16","210","","210","","","","","","","","","6","C 1 2/c 1","-C 2yc","15","","PbCd","","- C9 H5 Cd0.5 N4 O5 Pb -","- C9 H5 Cd0.5 N4 O5 Pb -","- C72 H40 Cd4 N32 O40 Pb8 -","8","1","","Wang, Xiyu; Yang, Guo-Ping; Wang, Yao-Yu","Catalytic comparison of cyanosilylation/Knoevenagel condensation reactions by Pb-based heterometallic organic frameworks with different second metal ions","Catalysis Science & Technology","2024","14","6","1613","1621","10.1039/D3CY01549A","","","0.71073","MoKα","","0.0284","0.0267","","","0.0703","0.0719","","","","","","1.091","","","","has coordinates,has disorder","290793","2024-04-04","22:20:55",""
"1571020","11.5184","0.0006","14.6526","0.0007","16.148","0.0009","97.73","0.003","108.931","0.002","98.573","0.003","2500","0.2","200","2","200","2","","","","","","","","4","P -1","-P 1","2","","","","- C94 H170 B6 O16 -","- C94 H170 B6 O16 -","- C94 H170 B6 O16 -","1","0.5","","Durin, Gabriel; Romero, R. Martin; Godou, Timothé; Chauvier, Clément; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault","Formoxyboranes as hydroborane surrogates for the catalytic reduction of carbonyls through transfer hydroboration","Catalysis Science & Technology","2024","14","7","1848","1853","10.1039/D3CY01702H","","","0.71073","MoKα","","0.0833","0.0643","","","0.1854","0.2003","","","","","","1.066","","","","has coordinates","290795","2024-04-04","22:21:21",""
"1571021","10.767","0.0002","12.8036","0.0005","18.9389","0.0008","90","","90","","90","","2610.85","0.16","150","2","150","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C14 H20 B N O2 -","- C14 H20 B N O2 -","- C112 H160 B8 N8 O16 -","8","1","","Durin, Gabriel; Romero, R. Martin; Godou, Timothé; Chauvier, Clément; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault","Formoxyboranes as hydroborane surrogates for the catalytic reduction of carbonyls through transfer hydroboration","Catalysis Science & Technology","2024","14","7","1848","1853","10.1039/D3CY01702H","","","0.71073","MoKα","","0.0466","0.0392","","","0.0962","0.1011","","","","","","1.045","","","","has coordinates","290795","2024-04-04","22:21:22",""
"1571022","9.8725","0.0005","7.3758","0.0004","21.882","0.0012","90","","98.551","0.003","90","","1575.68","0.15","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C16 H25 B N2 O2 -","- C16 H25 B N2 O2 -","- C64 H100 B4 N8 O8 -","4","1","","Durin, Gabriel; Romero, R. Martin; Godou, Timothé; Chauvier, Clément; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault","Formoxyboranes as hydroborane surrogates for the catalytic reduction of carbonyls through transfer hydroboration","Catalysis Science & Technology","2024","14","7","1848","1853","10.1039/D3CY01702H","","","0.71073","MoKα","","0.0446","0.0367","","","0.0971","0.1012","","","","","","1.065","","","","has coordinates","290795","2024-04-04","22:21:22",""
"1571023","12.5923","0.0008","10.8437","0.0006","14.9151","0.0008","90","","90.37","0.005","90","","2036.6","0.2","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H33 B N2 O2 -","- C20 H33 B N2 O2 -","- C80 H132 B4 N8 O8 -","4","1","","Durin, Gabriel; Romero, R. Martin; Godou, Timothé; Chauvier, Clément; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault","Formoxyboranes as hydroborane surrogates for the catalytic reduction of carbonyls through transfer hydroboration","Catalysis Science & Technology","2024","14","7","1848","1853","10.1039/D3CY01702H","","","0.71073","MoKα","","0.0708","0.0421","","","0.1013","0.1112","","","","","","0.989","","","","has coordinates","290795","2024-04-04","22:21:22",""
"1571024","10.1407","0.0004","28.0242","0.0011","12.2214","0.0005","90","","94.627","0.003","90","","3461.8","0.2","150","2","150","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C18 H28 B N O2 -","- C18 H28 B N O2 -","- C144 H224 B8 N8 O16 -","8","2","","Durin, Gabriel; Romero, R. Martin; Godou, Timothé; Chauvier, Clément; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault","Formoxyboranes as hydroborane surrogates for the catalytic reduction of carbonyls through transfer hydroboration","Catalysis Science & Technology","2024","14","7","1848","1853","10.1039/D3CY01702H","","","0.71073","MoKα","","0.0572","0.0396","","","0.0928","0.0993","","","","","","1.049","","","","has coordinates","290795","2024-04-04","22:21:22",""
"1571217","4.3844","0.0001","16.88","0.0003","23.4788","0.0004","90","","91.0715","0.0019","90","","1737.33","0.06","150","0.1","150","0.1","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C18 H16 F3 N O5 -","- C18.001 H16 F3.0015 N O5.001 -","- C72.004 H64 F12.006 N4 O20.004 -","4","1","","Wang, Yu; Li, Yiwen; Ni, Yeke; Bučar, Dejan-Krešimir; Dalby, Paul A.; Ward, John M.; Jeffries, Jack W. E.; Hailes, Helen C.","A transaminase-mediated aldol reaction and applications in cascades to styryl pyridines.","Catalysis science & technology","2024","14","9","2390","2399","10.1039/d3cy01370g","","x-ray","1.54184","CuKα","","0.0501","0.045","","","0.11","0.1134","","","","","","1.073","","","","has coordinates,has disorder","292757","2024-07-05","12:58:52",""
"1571255","13.4985","0.0008","16.3402","0.0011","8.5914","0.0004","90","","99.883","0.005","90","","1866.87","0.19","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H18 Br N3 O2 -","- C20 H18 Br N3 O2 -","- C80 H72 Br4 N12 O8 -","4","1","","Vijayakumar, Monica; Yhobu, Zhoveta; Małecki, Jan Grzegorz; Nagaraju, Dodahhali H.; Keri, Rangappa S.; Budagumpi, Srinivasa","Comprehensive enhancement in electrocatalytic oxygen evolution performance of nickel and cobalt complexes derived from π-conjugated N-heterocyclic carbene ligands through carbon composite strategy","Catalysis Science & Technology","2024","14","9","2489","2502","10.1039/D3CY01732J","","x-ray","0.71073","MoKα","","0.1038","0.0518","","","0.0995","0.1182","","","","","","1.039","","","","has coordinates","292758","2024-07-05","12:59:01",""
"1571256","10.7857","0.0016","14.519","0.002","11.7467","0.0018","90","","103.727","0.015","90","","1787","0.5","295","2","295","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C20 H18 Br N3 O2 -","- C20 H18 Br N3 O2 -","- C80 H72 Br4 N12 O8 -","4","1","","Vijayakumar, Monica; Yhobu, Zhoveta; Małecki, Jan Grzegorz; Nagaraju, Dodahhali H.; Keri, Rangappa S.; Budagumpi, Srinivasa","Comprehensive enhancement in electrocatalytic oxygen evolution performance of nickel and cobalt complexes derived from π-conjugated N-heterocyclic carbene ligands through carbon composite strategy","Catalysis Science & Technology","2024","14","9","2489","2502","10.1039/D3CY01732J","","x-ray","0.71073","MoKα","","0.1052","0.0525","","","0.1102","0.1385","","","","","","0.973","","","","has coordinates","292758","2024-07-05","12:59:02",""
"1571407","10.6039","0.0003","8.8338","0.0002","15.3191","0.0003","90","","92.902","0.002","90","","1433.14","0.06","100.01","0.1","100.01","0.1","","","","","","","","4","P 1 21 1","P 2yb","4","","(3R,5S)-5-([1,1'-biphenyl]-4-ylmethyl)-3-methylpyrrolidin-2-one","","- C18 H19 N O -","- C18 H19 N O -","- C72 H76 N4 O4 -","4","2","","Chen, Long; Qu, Ge; Cai, Zhiqiang; Yuan, Bo; Sun, Zhoutong","Synthesis of a sacubitril precursor via the construction of one-pot chemoenzymatic cascades","Catalysis Science & Technology","2024","14","10","2817","2824","10.1039/D4CY00145A","","x-ray","1.54184","CuKα","","0.0405","0.0355","","","0.1035","0.1061","","","","","","1.14","","","","has coordinates","292753","2024-07-05","12:57:37",""
"1571418","17.6518","0.0002","9.34996","0.00012","24.7713","0.0003","90","","105.336","0.0014","90","","3942.77","0.09","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C48 H38 Mg N4 O -","- C48 H38 Mg N4 O -","- C192 H152 Mg4 N16 O4 -","4","1","","Meher, Sushanta Kumar; Nayak, Prakash; Dhala, Sasmita; Tripathy, Swetapadma; Venkatasubbaiah, Krishnan","Magnesium-porphyrin as an efficient photocatalyst for the transformation of CO2 to cyclic carbonates and oxazolidinones under ambient conditions","Catalysis Science & Technology","2024","14","11","3125","3130","10.1039/D4CY00246F","","x-ray","1.54184","CuKα","","0.0606","0.0546","","","0.1621","0.1685","","","","","","1.0418","","","","has coordinates,has disorder","292759","2024-07-05","12:59:37",""
"1571676","11.3465","0.0002","12.5357","0.0002","13.0549","0.0002","109.944","0.002","101.745","0.001","105.832","0.001","1586.41","0.06","100","0.1","100","0.1","","","","","","","","6","P -1","-P 1","2","","Cr(OSi(tBu)3)2(XyNC)4","","- C60 H90 Cr N4 O8 Si2 -","- C60 H90 Cr N4 O8 Si2 -","- C60 H90 Cr N4 O8 Si2 -","1","0.5","","Kakiuchi, Yuya; Shapovalova, Svetlana; Protsenko, Bogdan; Guda, Sergey; Safonova, Olga V.; Guda, Alexander; Copéret, Christophe","Influence of strong π-acceptor ligands on Cr-K-edge X-ray absorption spectral signatures and consequences for the interpretation of surface sites in the Phillips catalyst.","Catalysis science & technology","2024","14","13","3682","3690","10.1039/d3cy01692g","","x-ray","1.54184","CuKα","","0.0336","0.0322","","","0.1089","0.1118","","","","","","0.996","","","","has coordinates","292756","2024-07-05","12:58:40",""
"1571677","10.928","0.0004","28.6868","0.001","14.0779","0.0006","90","","110.037","0.005","90","","4146.1","0.3","100","0.1","100","0.1","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","Cr(O(tBu)2C6H3)2(XyNC)2","","- C46 H60 Cr N2 O2 -","- C46 H60 Cr N2 O2 -","- C184 H240 Cr4 N8 O8 -","4","1","","Kakiuchi, Yuya; Shapovalova, Svetlana; Protsenko, Bogdan; Guda, Sergey; Safonova, Olga V.; Guda, Alexander; Copéret, Christophe","Influence of strong π-acceptor ligands on Cr-K-edge X-ray absorption spectral signatures and consequences for the interpretation of surface sites in the Phillips catalyst.","Catalysis science & technology","2024","14","13","3682","3690","10.1039/d3cy01692g","","x-ray","1.54184","CuKα","","0.068","0.0612","","","0.1456","0.1488","","","","","","1.108","","","","has coordinates","292756","2024-07-05","12:58:42",""
"1571678","13.1907","0.0003","20.8362","0.0005","23.4449","0.0006","90","","90","","90","","6443.7","0.3","100","0.1","100","0.1","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","Cr(OSi(tBu)3)3(XyNC)2","","- C54 H99 Cr N2 O12 Si3 -","- C54 H99 Cr N2 O12 Si3 -","- C216 H396 Cr4 N8 O48 Si12 -","4","1","","Kakiuchi, Yuya; Shapovalova, Svetlana; Protsenko, Bogdan; Guda, Sergey; Safonova, Olga V.; Guda, Alexander; Copéret, Christophe","Influence of strong π-acceptor ligands on Cr-K-edge X-ray absorption spectral signatures and consequences for the interpretation of surface sites in the Phillips catalyst.","Catalysis science & technology","2024","14","13","3682","3690","10.1039/d3cy01692g","","x-ray","1.54184","CuKα","","0.0854","0.0835","","","0.1905","0.1915","","","","","","1.104","","","","has coordinates,has disorder","292756","2024-07-05","12:58:42",""
"1571723","16.7116","0.0001","14.0718","0.0001","15.4454","0.0001","90","","96.098","0.001","90","","3611.62","0.04","100","0.1","100","0.1","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C42 H32 F6 Fe Ir N4 P -","- C42 H32 F6 Fe Ir N4 P -","- C168 H128 F24 Fe4 Ir4 N16 P4 -","4","1","","Gayen, Firdaus Rahaman; Chawla, Sakshi; Bora, Debashree; Borkotoky, Lodsna; Gazi, Sarifuddin; Mallick, Dibyendu; Maurya, Ram Awatar; De, Arijit Kumar; Saha, Biswajit","Boosting photocatalytic efficiency of iridium polypyridyl complex in coupling reaction through the induction of ferrocene: insights into bimetallic catalysis","Catalysis Science & Technology","2024","14","13","3618","3628","10.1039/D3CY01418E","","","1.54184","CuKα","","0.0364","0.0338","","","0.0906","0.0925","","","","","","1.049","","","","has coordinates","292754","2024-07-05","12:57:54",""
"1571727","9.2861","0.0003","15.141","0.0005","15.1451","0.0006","118.4","0.001","95.188","0.001","95.18","0.001","1843.74","0.11","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C16 H23 Co I2 N2 -","- C16 H23 Co I2 N2 -","- C64 H92 Co4 I8 N8 -","4","2","","Trotta, Caterina; Dahiya, Pardeep; Baldinelli, Lorenzo; Menendez Rodriguez, Gabriel; Chakraborty, Priyanka; Bistoni, Giovanni; De Angelis, Filippo; Sundararaju, Basker; Macchioni, Alceo","A cobalt molecular catalyst for hydrogen evolution reaction with remarkable activity in phosphate buffered water solution","Catalysis Science & Technology","2024","14","13","3699","3706","10.1039/D4CY00209A","","","0.71073","MoKα","","0.0618","0.0382","","","0.1072","0.1362","","","","","","0.83","","","","has coordinates","292755","2024-07-05","12:58:19",""
"1571728","8.202","0.0007","9.8816","0.0009","12.3164","0.0011","89.106","0.002","83.431","0.002","76.17","0.002","962.86","0.15","273.15","","273.15","","","","","","","","","5","P -1","-P 1","2","","Complex-2","","- C17 H25 Co I2 N2 -","- C17 H25 Co I2 N2 -","- C34 H50 Co2 I4 N4 -","2","1","","Trotta, Caterina; Dahiya, Pardeep; Baldinelli, Lorenzo; Menendez Rodriguez, Gabriel; Chakraborty, Priyanka; Bistoni, Giovanni; De Angelis, Filippo; Sundararaju, Basker; Macchioni, Alceo","A cobalt molecular catalyst for hydrogen evolution reaction with remarkable activity in phosphate buffered water solution","Catalysis Science & Technology","2024","14","13","3699","3706","10.1039/D4CY00209A","","x-ray","0.71073","MoKα","","0.0307","0.0269","","","0.0913","0.1","","","","","","0.7766","","","","has coordinates","292755","2024-07-05","12:58:26",""
"1571885","11.4614","0.0006","12.9693","0.0005","15.9143","0.0006","101.429","0.003","106.498","0.004","92.924","0.004","2208.7","0.18","293","2","293","2","","","","","","","","5","P 1","P 1","1","Co(II)-RibN2","8","","- C98 H123 Co2 N4 O10 -","- C98 H123 Co2 N4 O10 -","- C98 H123 Co2 N4 O10 -","1","1","","Pandey, Sachchida Nand; Sengupta, Arunava; Bera, Rajib; Ali, Sohel; Yadav, Somnath","A sugar-derived ligand for room temperature aerial oxidation or non-aqueous Markovnikov hydration of styrenes using a preformed or in situ generated Co complex","Catalysis Science & Technology","2024","14","16","4487","4495","10.1039/D4CY00522H","","x-ray","0.71073","MoKα","","0.0499","0.0395","","","0.0893","0.0953","","","","","","1.033","","","","has coordinates","294399","2024-09-05","22:48:40",""
"1572058","9.03","0.02","10.515","0.019","14.25","0.019","103.95","0.11","106.54","0.08","97.14","0.12","1231","4","293","2","293","2","","","","","","","","7","P -1","-P 1","2","","","","- C14 H19 Br Cl6 N2 Pd Sn -","- C14 H19 Br Cl6 N2 Pd Sn -","- C28 H38 Br2 Cl12 N4 Pd2 Sn2 -","2","1","","Nayak, Mukesh Kumar; Maharana, Rajat Rajiv; Mohanty, Anuradha; Samanta, Kousik; Roy, Sujit","Effect of N-heterocyclic carbene in palladium–tin heterobimetallic catalysis: a DFT supported study on the C3–H functionalization of unprotected indoles","Catalysis Science & Technology","2024","14","16","4674","4683","10.1039/D4CY00224E","","","0.71073","MoKα","","0.0899","0.0598","","","0.1652","0.2002","","","","","","1.052","","","","has coordinates","294400","2024-09-05","22:48:53",""
"1572060","19.5712","0.0006","5.9154","0.0001","20.8266","0.0006","90","","115.442","0.004","90","","2177.3","0.12","100","2","100","2","","","","","","","","4","P 1 21/c 1","-P 2ybc","14","","","","- C27 H30 N2 O -","- C27 H30 N2 O -","- C108 H120 N8 O4 -","4","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","1.54184","CuKα","","0.044","0.0367","","","0.0886","0.0926","","","","","","1.025","","","","has coordinates","294398","2024-09-05","22:48:23",""
"1572061","9.5244","0.0005","27.728","0.001","10.4699","0.0005","90","","114.029","0.007","90","","2525.4","0.2","110","2","110","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H30 Fe N2 O4 -","- C30 H30 Fe N2 O4 -","- C120 H120 Fe4 N8 O16 -","4","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.0638","0.0417","","","0.09","0.1007","","","","","","1.046","","","","has coordinates","294398","2024-09-05","22:48:24",""
"1572062","11.1925","0.0005","28.2554","0.0008","12.9763","0.0006","90","","113.551","0.006","90","","3761.9","0.3","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C41.71 H50.77 Fe N3 O3 -","- C41.705 H50.77 Fe N3 O3 -","- C166.82 H203.08 Fe4 N12 O12 -","4","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.0916","0.0675","","","0.1425","0.1516","","","","","","1.125","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572063","10.59054","0.00012","15.4277","0.0002","23.2167","0.0003","101.099","0.0012","99.234","0.001","103.291","0.0008","3538.47","0.08","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C38 H40 F6 Fe N2 O4 -","- C38 H40 F6 Fe N2 O4 -","- C152 H160 F24 Fe4 N8 O16 -","4","2","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.1161","0.0855","","","0.231","0.2484","","","","","","1.049","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572064","10.7552","0.0004","11.5325","0.0003","14.6781","0.0006","106.515","0.003","110.781","0.004","94.22","0.003","1600.72","0.12","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C34 H32.5 F6 Fe N3.5 O3 -","- C33 H31 F6 Fe N3 O3 -","- C66 H62 F12 Fe2 N6 O6 -","2","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","1.54184","CuKα","","0.0619","0.0606","","","0.1657","0.1675","","","","","","1.054","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572065","18.6211","0.0006","16.9942","0.0004","32.0027","0.0008","90","","90","","90","","10127.3","0.5","100","2","100","2","","","","","","","","5","P b c a","-P 2ac 2ab","61","","","","- C29 H28 F6 N2 O -","- C29 H28 F6 N2 O -","- C464 H448 F96 N32 O16 -","16","2","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","1.54184","CuKα","","0.1081","0.0622","","","0.1503","0.1727","","","","","","1.015","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572066","12.3708","0.0003","12.4378","0.0002","13.3652","0.0003","99.388","0.002","97.45","0.002","109.19","0.002","1878.73","0.08","100","2","100","2","","","","","","","","6","P -1","-P 1","2","","","","- C39 H47 Cl3 Fe N2 O4 -","- C39 H47 Cl3 Fe N2 O4 -","- C78 H94 Cl6 Fe2 N4 O8 -","2","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","1.54184","CuKα","","0.0326","0.0322","","","0.0859","0.0862","","","","","","1.083","","","","has coordinates","294398","2024-09-05","22:48:24",""
"1572067","11.1854","0.0005","12.6987","0.0005","14.8312","0.0007","86.447","0.004","71.724","0.004","71.449","0.004","1894.75","0.16","101","2","101","2","","","","","","","","5","P -1","-P 1","2","","","","- C42 H56 Fe N3 O3 -","- C42 H56 Fe N3 O3 -","- C84 H112 Fe2 N6 O6 -","2","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.1178","0.0847","","","0.1506","0.1632","","","","","","1.089","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572068","9.9427","0.0002","10.8687","0.0002","16.2473","0.0003","105.165","0.001","92.602","0.001","114.222","0.002","1521.98","0.06","100","2","100","2","","","","","","","","5","P -1","-P 1","2","","","","- C34 H38 Fe N2 O4 -","- C34 H38 Fe N2 O4 -","- C68 H76 Fe2 N4 O8 -","2","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.0371","0.0302","","","0.086","0.0885","","","","","","1.057","","","","has coordinates","294398","2024-09-05","22:48:24",""
"1572069","11.389","0.0005","28.6159","0.0007","10.6867","0.0005","90","","117.667","0.005","90","","3084.6","0.3","100","2","100","2","","","","","","","","5","P 1 21/c 1","-P 2ybc","14","","","","- C34.5 H37 Fe N3 O3 -","- C34.5 H37 Fe N3 O3 -","- C138 H148 Fe4 N12 O12 -","4","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.0724","0.0522","","","0.1229","0.1312","","","","","","1.056","","","","has coordinates,has disorder","294398","2024-09-05","22:48:24",""
"1572070","7.1127","0.0002","14.31","0.0004","21.7165","0.0006","90","","98.189","0.003","90","","2187.83","0.11","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C25 H23 Fe N3 O3 -","- C25 H23 Fe N3 O3 -","- C100 H92 Fe4 N12 O12 -","4","1","","Körner, Lukas; Bockfeld, Dirk; Bannenberg, Thomas; Tamm, Matthias","2,3-Diamino-4,5-diarylcyclopentadienone iron carbonyl complexes as catalysts for reductive amination reactions","Catalysis Science & Technology","2024","14","16","4522","4532","10.1039/D4CY00372A","","x-ray","0.71073","MoKα","","0.0484","0.0356","","","0.0942","0.0987","","","","","","1.056","","","","has coordinates","294398","2024-09-05","22:48:24",""
"1572204","9.529","0.0006","9.7708","0.0006","13.6707","0.0009","93.325","0.002","107.464","0.002","114.272","0.002","1082.49","0.12","203","2","203","2","","","","","","","","6","P 1","P 1","1","","","","- C44 H49 Br2 Cl2 N3 Ni -","- C44 H49 Br2 Cl2 N3 Ni -","- C44 H49 Br2 Cl2 N3 Ni -","1","1","","Norouzinyanlakvan, Somayeh; Ovens, Jeffrey; Richeson, Darrin","Electrocatalytic reduction of nitrite to ammonium ion using Ni(ii) complexes with redox-active di(imino)pyridine ligands","Catalysis Science & Technology","2024","14","18","5422","5429","10.1039/D4CY00715H","","","0.71073","MoKα","","0.0321","0.0296","","","0.0732","0.0749","","","","","","1.031","","","","has coordinates","295087","2024-10-06","04:17:11",""
"1572223","9.7333","0.0001","15.2824","0.0002","16.1184","0.0002","90","","91.158","0.001","90","","2397.09","0.05","100","2","100","2","","","","","","","","5","P 1 21/n 1","-P 2yn","14","","","","- C30 H25 N O2 S -","- C30 H25 N O2 S -","- C120 H100 N4 O8 S4 -","4","1","","Chikunova, Elena I.; Kotikova, Polina F.; Dar'in, Dmitry V.; Kukushkin, Vadim Yu.; Dubovtsev, Alexey Yu.","Coinage (Au, Ag, Cu) metal-catalyzed (3 + 2) annulation of α-aminoketones and electron-deficient alkynes as a route to 3-EWG-substituted pyrroles","Catalysis Science & Technology","2024","14","19","5671","5677","10.1039/D4CY00660G","","","1.54184","CuKα","","0.0431","0.0395","","","0.1098","0.1126","","","","","","1.09","","","","has coordinates","295085","2024-10-06","04:15:06",""
"1572224","9.2439","0.0002","14.8214","0.0004","28.8605","0.0007","90","","90","","90","","3954.11","0.17","100","2","100","2","","","","","","","","5","P 21 21 21","P 2ac 2ab","19","","","","- C49 H40 N2 O4 S -","- C49 H40 N2 O4 S -","- C196 H160 N8 O16 S4 -","4","1","","Chikunova, Elena I.; Kotikova, Polina F.; Dar'in, Dmitry V.; Kukushkin, Vadim Yu.; Dubovtsev, Alexey Yu.","Coinage (Au, Ag, Cu) metal-catalyzed (3 + 2) annulation of α-aminoketones and electron-deficient alkynes as a route to 3-EWG-substituted pyrroles","Catalysis Science & Technology","2024","14","19","5671","5677","10.1039/D4CY00660G","","x-ray","1.54184","CuKα","","0.0372","0.0355","","","0.095","0.0959","","","","","","1.073","","","","has coordinates","295085","2024-10-06","04:15:21",""
"1572225","13.71","0.03","8.846","0.019","16.24","0.03","90","","93.51","0.18","90","","1966","7","296","2","296","2","","","","","","","","3","I 1 2/c 1","-I 2yc","15","","","","- C24 H18 O6 -","- C24 H18 O6 -","- C96 H72 O24 -","4","0.5","","Biswas, Subir; Barman, Dipankar; Dutta, Priyanka; Gour, Nand K.; Lee, Seonghwan; Kim, Donguk; Park, Young-Bin; Bora, Tonmoy J.; Devi, Arpita; Khanam, Salma A.; Saikia, Lakshi; Karunakar, Galla V.; Zaki, Magdi E. A.; Bania, Kusum K.","Ru-nanoparticles supported on zeolite-Y for ortho-benzylation of phenols and activation of H2O2 for selective synthesis of BINOLs","Catalysis Science & Technology","2024","14","18","5234","5256","10.1039/D4CY00429A","","","0.71073","MoKα","","0.3392","0.0953","","","0.1301","0.1902","","","","","","1.063","","","","has coordinates","295088","2024-10-06","04:17:58",""
"1572236","10.888","0.001","7.319","0.001","11.07","0.001","90","","91.77","0.01","90","","881.74","0.17","198","2","198","2","","","","","","","","4","P 1 21 1","P 2yb","4","","","","- C22 H25 Fe N -","- C22 H25 Fe N -","- C44 H50 Fe2 N2 -","2","1","","Cao, Xu-You; Xu, Shi-Yin; Wu, Ling-Wei; Qiu, Yi-Feng; Zhang, Hao; Si, Li-Ping; Wang, Li-Ming; Liu, Hai-Yang","Co(iii) corroles with pendant amidophenol and amidopyridine as proton-relay arms to facilitate the electrocatalytic hydrogen evolution reaction","Catalysis Science & Technology","2024","14","19","5608","5615","10.1039/D4CY00677A","","","0.71073","MoKα","","0.0703","0.0476","","","0.0779","0.0852","","","","","","1.044","","","","has coordinates","295084","2024-10-06","04:13:28",""
"1572237","8.8638","0.0003","27.6166","0.001","22.2046","0.0008","90","","93.367","0.001","90","","5426","0.3","170","","170","","","","","","","","","7","P 1 21/c 1","-P 2ybc","14","","","","- C65 H36 Co F10 N4 O2 P -","- C65 H36 Co F10 N4 O2 P -","- C260 H144 Co4 F40 N16 O8 P4 -","4","1","","Cao, Xu-You; Xu, Shi-Yin; Wu, Ling-Wei; Qiu, Yi-Feng; Zhang, Hao; Si, Li-Ping; Wang, Li-Ming; Liu, Hai-Yang","Co(iii) corroles with pendant amidophenol and amidopyridine as proton-relay arms to facilitate the electrocatalytic hydrogen evolution reaction","Catalysis Science & Technology","2024","14","19","5608","5615","10.1039/D4CY00677A","","","0.71073","MoKα","","0.0911","0.0671","","","0.1758","0.1928","","","","","","1.053","","","","has coordinates","295084","2024-10-06","04:14:06",""
"1572249","12.7674","0.0005","17.7058","0.0007","15.0682","0.0006","90","","105.218","0.004","90","","3286.8","0.2","130","2","130","2","","","","","","","","6","P 1 21/n 1","-P 2yn","14","","","","- C32 H47 Cu N O3 P3 -","- C32 H47 Cu N O3 P3 -","- C128 H188 Cu4 N4 O12 P12 -","4","1","","Arévalo, Alma; Juárez-Francisco, Enrique; Roa, Diego A.; Flores-Alamo, Marcos; García, Juventino J.","New mononuclear Cu(i) compounds: synthesis, characterization, and application to the electroreduction of CO2","Catalysis Science & Technology","2024","14","18","5394","5404","10.1039/D4CY00759J","","","0.71073","MoKα","","0.0722","0.0539","","","0.1289","0.1436","","","","","","1.036","","","","has coordinates","295086","2024-10-06","04:16:16",""
"1572250","10.4119","0.0011","15.363","0.002","18.5644","0.0017","90","","90","","90","","2969.5","0.6","130","2","130","2","","","","","","","","6","P 21 21 21","P 2ac 2ab","19","","","","- C28 H39 Cu N O3 P3 -","- C28 H39 Cu N O3 P3 -","- C112 H156 Cu4 N4 O12 P12 -","4","1","","Arévalo, Alma; Juárez-Francisco, Enrique; Roa, Diego A.; Flores-Alamo, Marcos; García, Juventino J.","New mononuclear Cu(i) compounds: synthesis, characterization, and application to the electroreduction of CO2","Catalysis Science & Technology","2024","14","18","5394","5404","10.1039/D4CY00759J","","","0.71073","MoKα","","0.0934","0.0535","","","0.0674","0.0821","","","","","","1.088","","","","has coordinates","295086","2024-10-06","04:16:30",""
"1572251","8.6246","0.0007","9.3841","0.0006","17.1248","0.001","91.601","0.005","97.997","0.006","100.216","0.006","1348.77","0.16","130","2","130","2","","","","","","","","7","P -1","-P 1","2","","","","- C22 H36 Cu Fe N O3 P2 -","- C22 H36 Cu Fe N O3 P2 -","- C44 H72 Cu2 Fe2 N2 O6 P4 -","2","1","","Arévalo, Alma; Juárez-Francisco, Enrique; Roa, Diego A.; Flores-Alamo, Marcos; García, Juventino J.","New mononuclear Cu(i) compounds: synthesis, characterization, and application to the electroreduction of CO2","Catalysis Science & Technology","2024","14","18","5394","5404","10.1039/D4CY00759J","","","0.71073","MoKα","","0.0512","0.0335","","","0.0646","0.0722","","","","","","1.032","","","","has coordinates","295086","2024-10-06","04:16:30",""
"1572997","9.7622","0.0002","11.3546","0.0002","20.4691","0.0003","90","","90.507","0.002","90","","2268.83","0.07","150","0.1","150","0.1","","","","","","","","4","P 1 21/n 1","-P 2yn","14","","","","- C26 H22 N5 P -","- C26 H22 N5 P -","- C104 H88 N20 P4 -","4","1","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","x-ray","0.71073","MoKα","","0.0348","0.0318","","","0.0794","0.0817","","","","","","1.037","","","","has coordinates","295734","2024-11-03","23:17:21",""
"1572998","8.5305","0.0004","9.4375","0.0004","17.6861","0.0006","90.703","0.003","98.984","0.003","99.254","0.004","1387.06","0.1","273.15","0.1","273.15","0.1","","","","","","","","9","P -1","-P 1","2","","","","- C27 H22 Cl F3 N5 Ni O3 P S -","- C27 H22 Cl F3 N5 Ni O3 P S -","- C54 H44 Cl2 F6 N10 Ni2 O6 P2 S2 -","2","1","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","x-ray","0.71073","MoKα","","0.1065","0.0576","","","0.1101","0.1262","","","","","","1.025","","","","has coordinates","295734","2024-11-03","23:17:23",""
"1572999","21.2519","0.0014","10.0002","0.0005","24.7491","0.0015","90","","114.089","0.007","90","","4801.7","0.6","150","0.1","150","0.1","","","","","","","","6","I 1 2/a 1","-I 2ya","15","","","","- C25 H19 Cl N5 Ni P -","- C25 H19 Cl N5 Ni P -","- C200 H152 Cl8 N40 Ni8 P8 -","8","1","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","x-ray","0.71073","MoKα","","0.0896","0.0546","","","0.1331","0.1599","","","","","","0.986","","","","has coordinates","295734","2024-11-03","23:17:23",""
"1573000","17.3501","0.0008","10.6515","0.0005","14.9182","0.0006","90","","90","","90","","2757","0.2","150","2","150","","","","","","","","","9","P n a 21","P 2c -2n","33","","","","- C22 H28 Cl F3 N5 Ni O3 P S -","- C22 H28 Cl F3 N5 Ni O3 P S -","- C88 H112 Cl4 F12 N20 Ni4 O12 P4 S4 -","4","1","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","","0.71073","MoKα","","0.0519","0.0389","","","0.0816","0.0876","","","","","","1.005","","","","has coordinates","295734","2024-11-03","23:17:23",""
"1573001","7.8912","0.0007","8.8336","0.001","18.4362","0.0019","85.707","0.004","85.978","0.004","74.077","0.004","1230.7","0.2","113","","113","","","","","","","","","7","P -1","-P 1","2","","","","- C48 H62 Cl2 N10 Ni2 O P2 -","- C48 H62 Cl2 N10 Ni2 O P2 -","- C48 H62 Cl2 N10 Ni2 O P2 -","1","0.5","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","","0.71073","MoKα","","0.0318","0.0264","","","0.0621","0.0647","","","","","","1.028","","","","has coordinates,has disorder","295734","2024-11-03","23:17:23",""
"1573002","42.93","0.003","42.93","0.003","16.9889","0.0015","90","","90","","120","","27116","4","293.15","","293.15","","","","","","","","","9","R -3 :H","-R 3","148","","","","- C52 H40 Cl2 F6 N10 Ni2 O6 P2 S2 -","- C52 H40 Cl2 F6 N10 Ni2 O6 P2 S2 -","- C936 H720 Cl36 F108 N180 Ni36 O108 P36 S36 -","18","1","","Mohite, Manali A.; Sheokand, Sonu; Balakrishna, Maravanji S.","Nickel–PNN catalysed sustainable synthesis of polysubstituted quinolines under microwave irradiation","Catalysis Science & Technology","2024","14","20","5959","5969","10.1039/D4CY00863D","","","0.71073","MoKα","","0.1178","0.0596","","","0.1314","0.1636","","","","","","1.025","","","","has coordinates","295734","2024-11-03","23:17:23",""