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1

Rödl, Thomas, and Arno Pfitzner. "(AuI)3P4Se5: Ein Addukt von polymerem P4Se5mit AuI." Zeitschrift für anorganische und allgemeine Chemie 634, no. 11 (September 2008): 2072. http://dx.doi.org/10.1002/zaac.200870127.

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2

Smirnova, Ekaterina S., José M. Muñoz Molina, Alice Johnson, Nuno A. G. Bandeira, Carles Bo, and Antonio M. Echavarren. "Polynuclear Gold [AuI ]4 , [AuI ]8 , and Bimetallic [AuI 4 AgI ] Complexes: C−H Functionalization of Carbonyl Compounds and Homogeneous Carbonylation of Amines." Angewandte Chemie 128, no. 26 (May 11, 2016): 7613–17. http://dx.doi.org/10.1002/ange.201603200.

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3

Smirnova, Ekaterina S., José M. Muñoz Molina, Alice Johnson, Nuno A. G. Bandeira, Carles Bo, and Antonio M. Echavarren. "Polynuclear Gold [AuI ]4 , [AuI ]8 , and Bimetallic [AuI 4 AgI ] Complexes: C−H Functionalization of Carbonyl Compounds and Homogeneous Carbonylation of Amines." Angewandte Chemie International Edition 55, no. 26 (May 11, 2016): 7487–91. http://dx.doi.org/10.1002/anie.201603200.

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4

Jiang, Xuan-Feng, Franky Ka-Wah Hau, Qing-Fu Sun, Shu-Yan Yu, and Vivian Wing-Wah Yam. "From {AuI···AuI}-Coupled Cages to the Cage-Built 2-D {AuI···AuI} Arrays: AuI···AuIBonding Interaction Driven Self-Assembly and Their AgISensing and Photo-Switchable Behavior." Journal of the American Chemical Society 136, no. 31 (July 25, 2014): 10921–29. http://dx.doi.org/10.1021/ja502295c.

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5

Koshevoy, Igor O., Antti J. Karttunen, Ilya S. Kritchenkou, Dmitrii V. Krupenya, Stanislav I. Selivanov, Alexei S. Melnikov, Sergey P. Tunik, Matti Haukka, and Tapani A. Pakkanen. "Sky-Blue Luminescent AuI–AgI Alkynyl-Phosphine Clusters." Inorganic Chemistry 52, no. 7 (March 21, 2013): 3663–73. http://dx.doi.org/10.1021/ic302105a.

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6

Joyce, Liam M., Anthony C. Willis, Christopher J. T. Hyland, and Stephen G. Pyne. "Gold- and Silver-Catalysed Cyclisation Reactions of β-Amino Allenes." Australian Journal of Chemistry 71, no. 9 (2018): 682. http://dx.doi.org/10.1071/ch18197.

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Herein we report the formation of pyrrolines and tetrahydropyridines from the cyclisation reactions of β-amino allenes by both AuI and AgI catalysts in yields ranging from 5 to 70 %. AuI catalysts favour a 5-endo-dig cyclisation before rapid rearrangement to the 5-exo-dig product, while AgI favours a 6-endo-trig cyclisation. We also report the first known Ag2O catalysed cyclisation reaction of an allene which occurred in good yield (61 %).
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7

Mu, Xiaoyue, Dong Liu, Xiao Cheng, Lu Li, Hongyu Zhang, and Yue Wang. "AuI⋯AuI interaction induced semiconducting microwires with photo- and vapor-responsive properties." Organic Electronics 13, no. 3 (March 2012): 457–63. http://dx.doi.org/10.1016/j.orgel.2011.11.013.

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8

Barakat, Khaldoon, and Thomas R. Cundari. "Chemical and photophysical properties of AuI, AuII, AuIII, and AuI-dimer complexes." Chemical Physics 311, no. 1-2 (April 2005): 3–11. http://dx.doi.org/10.1016/j.chemphys.2004.10.017.

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9

García-Fernández, Pedro D., Javier Iglesias-Sigüenza, Paula S. Rivero-Jerez, Elena Díez, Enrique Gómez-Bengoa, Rosario Fernández, and José M. Lassaletta. "AuI-Catalyzed Hydroalkynylation of Haloalkynes." Journal of the American Chemical Society 142, no. 37 (August 19, 2020): 16082–89. http://dx.doi.org/10.1021/jacs.0c07951.

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10

Carvajal, M. A., J. J. Novoa, and S. Alvarez. "The nature of the AuI ... AuI Interactions between Cationic [AuL2]+ Complexes in the Solid State." Theoretical Chemistry Accounts 116, no. 4-5 (February 21, 2006): 472–79. http://dx.doi.org/10.1007/s00214-006-0083-7.

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11

Koshevoy, Igor O., Antti J. Karttunen, Julia R. Shakirova, Alexei S. Melnikov, Matti Haukka, Sergey P. Tunik, and Tapani A. Pakkanen. "Halide-Directed Assembly of Multicomponent Systems: Highly Ordered AuI-AgI Molecular Aggregates." Angewandte Chemie 122, no. 47 (October 8, 2010): 9048–50. http://dx.doi.org/10.1002/ange.201004386.

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12

Koshevoy, Igor O., Antti J. Karttunen, Julia R. Shakirova, Alexei S. Melnikov, Matti Haukka, Sergey P. Tunik, and Tapani A. Pakkanen. "Halide-Directed Assembly of Multicomponent Systems: Highly Ordered AuI-AgI Molecular Aggregates." Angewandte Chemie International Edition 49, no. 47 (October 8, 2010): 8864–66. http://dx.doi.org/10.1002/anie.201004386.

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13

Siemeling, Ulrich, Thorsten Klemann, Clemens Bruhn, Jiří Schulz, and Petr Štěpnička. "The Coordination Behaviour of Ferrocene-based Pyridylphosphine Ligands towards AgI and AuI." Zeitschrift für anorganische und allgemeine Chemie 637, no. 12 (August 11, 2011): 1824–33. http://dx.doi.org/10.1002/zaac.201100209.

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14

Reynard, Linda M., Corey J. Evans, and Michael C. L. Gerry. "The Pure Rotational Spectrum of AuI." Journal of Molecular Spectroscopy 205, no. 2 (February 2001): 344–46. http://dx.doi.org/10.1006/jmsp.2000.8274.

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15

Liu, Xipei, and James Bagrow. "Autocompletion interfaces make crowd workers slower, but their use promotes response diversity." Human Computation 6 (June 2, 2019): 42–55. http://dx.doi.org/10.15346/hc.v6i1.89.

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Creative tasks such as ideation or question proposal are powerful applications of crowdsourcing, yet the quantity of workers available for addressing practical problems is often insufficient. To enable scalable crowdsourcing thus requires gaining all possible efficiency and information from available workers. One option for text-focused tasks is to allow assistive technology, such as an autocompletion user interface (AUI), to help workers input text responses. But support for the efficacy of AUIs is mixed. Here we designed and conducted a randomized experiment where workers were asked to provide short text responses to given questions. Our experimental goal was to determine if an AUI helps workers respond more quickly and with improved consistency by mitigating typos and misspellings. Surprisingly, we found that neither occurred: workers assigned to the AUI treatment were slower than those assigned to the non-AUI control and their responses were more diverse, not less, than those of the control. Both the lexical and semantic diversities of responses were higher, with the latter measured using word2vec. A crowdsourcer interested in worker speed may want to avoid using an AUI, but using an AUI to boost response diversity may be valuable to crowdsourcers interested in receiving as much novel information from workers as possible.
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16

Sakai, H., S. Nakashima, T. Moriwaki, K. Yamada, and Y. Maeda. "I-129 and Au-197 Mössbauer Spectroscopy of AuI and AgAuI2." Zeitschrift für Naturforschung A 57, no. 6-7 (July 1, 2002): 575–80. http://dx.doi.org/10.1515/zna-2002-6-751.

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Mössbauer spectroscopy of 129I and 197Au nuclei has been applied for AuI and AgAuI2 to clarify the electronic structures of the gold and iodine atoms, and to investigate the nature of the Au-I bonds. In the 129I Mössbauer spectra the sign of e2qQ is positive for AuI, whereas the sign is negative for AgAuI2. This is attributable to the difference in molecular structures: The iodine atom in AuI is bridged by two gold atoms and in AgAuI2 the iodine is terminal. The 197Au Mössbauer spectra suggest that the Au-I bond in AgAuI2 is more covalent than that in AuI. We have revealed that AgAuI2 consists of Ag+ and linear [I-Au-I]- units from the Rietveld refinement of the X-ray powder diffraction pattern
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17

Jagdale, Arun R., and So Won Youn. "AuI-Catalyzed Intramolecular Cyclization of 2-Alkenylphenyl Carbonyl Compounds: Exploring the Oxophilic Lewis Acidity of AuI Species." European Journal of Organic Chemistry 2011, no. 20-21 (March 22, 2011): 3904–10. http://dx.doi.org/10.1002/ejoc.201100113.

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18

Marion, Nicolas, Ronan Gealageas, and Steven P. Nolan. "[(NHC)AuI]-Catalyzed Rearrangement of Allylic Acetates." Organic Letters 9, no. 14 (July 2007): 2653–56. http://dx.doi.org/10.1021/ol070843w.

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19

Stanek, Jan, S. S. Hafner, and Barbara Miczko. "Bonding ofAu+in AuI from Mössbauer spectroscopy." Physical Review B 57, no. 11 (March 15, 1998): 6219–22. http://dx.doi.org/10.1103/physrevb.57.6219.

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20

Mizushima, Eiichiro, Kazuhiko Sato, Teruyuki Hayashi, and Masato Tanaka. "Highly Efficient AuI-Catalyzed Hydration of Alkynes." Angewandte Chemie International Edition 41, no. 23 (December 2, 2002): 4563–65. http://dx.doi.org/10.1002/1521-3773(20021202)41:23<4563::aid-anie4563>3.0.co;2-u.

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21

Marion, Nicolas, Ronan Gealageas, and Steven P. Nolan. "[(NHC)AuI]-Catalyzed Rearrangement of Allylic Acetates." Organic Letters 10, no. 5 (March 2008): 1037. http://dx.doi.org/10.1021/ol800032e.

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22

Kovarik, Carrie, Ivy Lee, Justin Ko, Adewole Adamson, Clark Otley, Joseph Kvedar, Priyank Vedak, Susan Huang, Matthew Fitzgerald, and Rachna Chaudhari. "Commentary: Position statement on augmented intelligence (AuI)." Journal of the American Academy of Dermatology 81, no. 4 (October 2019): 998–1000. http://dx.doi.org/10.1016/j.jaad.2019.06.032.

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23

Zhao, W. Z., X. Y. Xu, W. Y. Ma, Y. Cheng, Q. Hui, K. L. Wen, and D. Y. Chen. "Experimental study of autoionizing states of AuI." Applied Physics B Photophysics and Laser Chemistry 52, no. 4 (April 1991): 299–304. http://dx.doi.org/10.1007/bf00325409.

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24

Bennett, Martin A., Nedaossadat Mirzadeh, Steven H. Privér, Jörg Wagler, and Suresh K. Bhargava. "Trinuclear Mixed-valent Gold Complexes Derived from 2-C6F4PPh2: Phosphine Oxide Complexes of Gold(III) and an ortho-Metallated Complex of Gold(I)." Zeitschrift für Naturforschung B 64, no. 11-12 (December 1, 2009): 1463–68. http://dx.doi.org/10.1515/znb-2009-11-1229.

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Crystals of two mixed-valent gold complexes [(O2NO)AuI(μ-2-C6F4PPh2)AuIII{κ2-2-C6- F4P(O)Ph2}(μ-2-C6F4PPh2)AuI(ONO2)] (14) and [(O2NO)AuI(μ-2-C6F4PPh2)AuIII{κ3-2-C6F4- P(O)Ph(C6H4)}(μ-2-C6F4PPh2)AuI] (15) have been obtained from the reaction of the digold(I,III) complex [ClAuI(μ-2-C6F4PPh2)(κ2-2-C6F4PPh2)AuIIICl] (5) with, respectively, a small and a large excess of silver nitrate. Both complexes contain three, approximately collinear metal atoms, the central gold(III) atom being planar-coordinated by a chelate (O,C)-phosphine oxide formed by oxidation of 2-C6F4PPh2 and the carbon atoms of two bridging 2-C6F4PPh2 groups. In 14 each of the terminal gold(I) atoms is coordinated by a monodentate nitrate ion and the phosphorus atom of μ-2-C6F4PPh2, whereas in 15 the nitrate ion on one of the gold(I) atoms of 14 has been replaced by the carbon atom of a bridging C6H4 group derived by Ag+-promoted cyclometallation of a phenyl group on the neighbouring phosphine oxide
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25

Jagdale, Arun R., and So Won Youn. "ChemInform Abstract: AuI-Catalyzed Intramolecular Cyclization of 2-Alkenylphenyl Carbonyl Compounds: Exploring the Oxophilic Lewis Acidity of AuI Species." ChemInform 42, no. 49 (November 10, 2011): no. http://dx.doi.org/10.1002/chin.201149093.

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26

Elkassaby, Mohammed, Mahmoud Alawy, Mohamed Zaki Ali, Wael A. Tawfick, and Sherif Sultan. "Aorto-Uni-Iliac Stent Grafts with and without Crossover Femorofemoral Bypass for Treatment of Abdominal Aortic Aneurysms: A Parallel Observational Comparative Study." International Journal of Vascular Medicine 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/962078.

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We investigated the safety and efficacy of primary aorto-uni-iliac (AUI) endovascular aortic repair (EVAR) without fem-fem crossover in patients with abdominal aortic aneurysm (AAA) and concomitant aortoiliac occlusive disease. 537 EVARs were implemented between 2002 and 2015 in University Hospital Galway, a tertiary referral center for aortic surgery and EVAR. We executed a parallel observational comparative study between 34 patients with AUI with femorofemoral crossover (group A) and six patients treated with AUI but without the crossover (group B). Group B patients presented with infrarenal AAAs with associated total occlusion of one iliac axis and high comorbidities. Technical success was 97% (n=33) in group A and 85% (n=5) in group B (P=0.31). Primary and assisted clinical success at 24 months were 88% (n=30) and 12% (n=4), respectively, in group A, and 85% (n=5) and 15% (n=1), respectively, in group B (P=0.125). Reintervention rate was 10% (n=3) in group A and 0% in group B (P=0.084). No incidence of postoperative critical lower limb ischemia or amputations occurred in the follow-up period. AUI without crossover bypass is a viable option in selected cases.
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27

Ghazzali, Mohamed, Mohammed H. Jaafar, Khalid Al-Farhan, Sebastiaan Akerboom, and Jan Reedijk. "Synthesis, structure and luminescence of new dinuclear cyanido-bridged AgI–AuI one-dimensional coordination polymer." Inorganic Chemistry Communications 20 (June 2012): 188–90. http://dx.doi.org/10.1016/j.inoche.2012.03.005.

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28

Bennett, M. A., S. K. Bhargava, F. Mohr, L. L. Welling, and A. C. Willis. "Synthesis and X-Ray Structure of a Heterovalent, Cycloaurated Pentafluorophenylgold(I)/Pentafluorophenylgold(III) Complex." Australian Journal of Chemistry 55, no. 4 (2002): 267. http://dx.doi.org/10.1071/ch02034.

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The heterovalent gold(I)/gold(III) complex [(C6F5)AuI(μ-2-Ph2PC6H3-6-Me)AuIII(C6F5){η2-(6-MeC6H3-2-PPh2)}] has been prepared and structurally characterized by X-ray crystallography. It shows square planar stereochemistry at AuIII incorporating a four-membered chelate ring and linear arrangement at AuI. The compound is a rare example of a heterovalent complex containing an aryl ligand on each gold atom.
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29

Cordero-Rivera, R. Evelyn, David Rendón-Nava, Carlos Ángel-Jijón, Oscar R. Suárez-Castillo, and Daniel Mendoza-Espinosa. "Synthesis and Reactivity of (NHC)AuI–Mercaptopyridine Complexes." Organometallics 39, no. 10 (March 31, 2020): 1887–95. http://dx.doi.org/10.1021/acs.organomet.0c00118.

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30

Takao, Hidenobu, Kaoru Sakai, Jun Osufi, and Hiroaki Ishii. "Acoustic User Interface (AUI) for the auditory displays." Displays 23, no. 1-2 (April 2002): 65–73. http://dx.doi.org/10.1016/s0141-9382(02)00011-2.

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31

Vellé, Alba, Ronan Maguire, Kevin Kavanagh, Pablo J. Sanz Miguel, and Diego Montagner. "Steroid-AuI -NHC Complexes: Synthesis and Antibacterial Activity." ChemMedChem 12, no. 11 (May 19, 2017): 841–44. http://dx.doi.org/10.1002/cmdc.201700257.

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32

Böge, Matthias, and Jürgen Heck. "Molecular Gold Wire from Mixed-Valent AuI/IIIComplexes." Chemistry - A European Journal 22, no. 20 (March 31, 2016): 6787–92. http://dx.doi.org/10.1002/chem.201600782.

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33

Shakirova, Julia R., Elena V. Grachova, Alexei S. Melnikov, Vladislav V. Gurzhiy, Sergey P. Tunik, Matti Haukka, Tapani A. Pakkanen, and Igor O. Koshevoy. "Toward Luminescence Vapochromism of Tetranuclear AuI–CuI Clusters." Organometallics 32, no. 15 (July 23, 2013): 4061–69. http://dx.doi.org/10.1021/om301100v.

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34

Hakaim, Albert G., W. Andrew Oldenburg, Ricardo Paz-Fumagalli, J. Mark McKinney, Louis Lau, Matthias Biebl, Josef Klocker, Beate Neuhauser, Beate Hugl, and Jergen Falkensammer. "Long-Term Results of Endovascular Aneurysm Repair with Aortouni-iliac Custom-Made Stent Grafts." Vascular 14, no. 3 (May 1, 2006): 136–41. http://dx.doi.org/10.2310/6670.2006.00023.

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The purpose of this study was to review the outcome of endovascular abdominal aortic aneurysm repair (EVAR) using custom-made aortouni-iliac (AUI) devices with femorofemoral bypass. Between June 1999 and March 2001, 23 consecutive patients (1 female, 22 male) at high risk of open aortic aneurysm repair underwent EVAR with custom devices in an AUI configuration. The mean follow-up was 37 months (range 2–72 months), and the mean age was 76.8 years (range 67.5–88.7 years). Increased surgical risk was evidenced by 92% and 69% of patients with significant pulmonary or cardiac disease, respectively. The preoperative mean aneurysm diameter ( n = 23) 62 ± 8.2 mm was significantly greater than the postoperative diameter, ( n = 23) 54 ± 16.4 mm. Ten endoleaks occurred. Migration of the stent graft occurred in 9% ( n = 2). Secondary interventions were necessary in 23%, whereas tertiary interventions were required in 9%. Patients at high risk of open aneurysm repair received sufficient protection from aneurysm rupture with custom-made AUI devices.
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35

Liau, Ruei-Yang, Trevor Mathieson, Annette Schier, Raphael J. F. Berger, Nino Runeberg, and Hubert Schmidbaur. "Structural, Spectroscopic and Theoretical Studies of (tButyl-isocyanide)gold(I) Iodide." Zeitschrift für Naturforschung B 57, no. 8 (August 1, 2002): 881–89. http://dx.doi.org/10.1515/znb-2002-0807.

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The complexes (tBuNC)AuCl and (tBuNC)AuI 13C-labeled at the isocyanide group were prepared and investigated by concentration- and temperature-dependent IR and NMR spectroscopy in dichloromethane solution. No indication for association of the molecules was obtained. The crystal structure of the iodide complex was determined by X-ray diffraction methods and shown to feature only monomers with extremely large intermolecular Au-Au contacts of 4.162 Å, well beyond the sum of the van der Waals radii. It therefore appears that (tBuNC)AuI is a rare example of a sterically non-hindered L-Au-X complex which shows no aurophilic interactions whatsoever. In a quantum-chemical analysis (at the local MP2 level) of the dimerization of the model compounds (MeNC)AuCl and (MeNC)AuI in various dimer geometries it was demonstrated that the energy-balance of the dimerization is very delicate and not dominated solely by contributions from correlation / relativistic (aurophilic) effects.
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36

Sevillano, Paloma, Abraha Habtemariam, M. Inés García Seijo, Alfonso Castiñeiras, Simon Parsons, M. Esther García, and Peter J. Sadler. "Homonuclear PdII and PtII and heteronuclear PdII-AuI and PtII-AuI complexes of a tripod triphosphine ligand: synthesis, characterization and reactions with molecules of biological relevance." Australian Journal of Chemistry 53, no. 8 (2000): 635. http://dx.doi.org/10.1071/ch00028.

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Complexes of the type Pd(tripod)X2 [tripod = MeC(CH2PPh2)3; X = Cl (1), Br (2), I (3)] and Pt(tripod)X2 [X = Cl (4), Br (5), I (6)] have been synthesized. In these complexes tripod acts as a bidentate chelating ligand. The uncoordinated phosphorus atom can bind to AuI to form the bimetallic complexes PdAu(tripod)X3 [X = Cl (7), Br (8), I (9)] and PtAu(tripod)X3 [X = Cl (10), Br (11), I (12)]. Complexes (1)–(12) have been characterized by microanalysis, f.a.b. mass spectrometry, i.r. spectroscopy, 31P and 195Pt n.m.r. spectroscopies, and conductivity measurements. The structures of complexes (1), (4) and (11), as well as that of the unusual complex Cl2Pt(tripod)AuBr0.5Cl0.5 (13), isolated from reaction of Pt(tripod)Br2 (5), and [Au(thiodiglycol)Cl], have been determined. All complexes show square-planar geometry for PdII or PtII and linear geometry for AuI. The X-ray crystal structure of (1) showed partial oxidation of the dangling phosphorus of the ligand in 50% of the molecule distributed randomly over the lattice. Reactions of complex (4), Pt(tripod)Cl2, with the tripeptide glutathione (GSH) showed the formation of [Pt2(tripod)2(GS-µ–S)2]2+ (15a). No reaction with N-acetyl-L-methionine (AcMet) or guanosine 5´-monophosphate (5´-GMP) was observed. Reactions of [Pt(tripod–O)(ONO2)2] (14) with GSH resulted in the formation of [Pt2(tripod–O)2(GS-µ-S)2]2+ (15b). Displacement of the S-containing molecules by 5´-GMP in the presence of AuI, via Pt–S bond cleavage, was observed for complex (15b). PtAu(tripod)Cl3 (10) reacted with GSH, with initial attack on the AuI centre.
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37

Chen, Zheng, Yinjuan Chen, Songlin Chao, Xiaobin Dong, Wenxing Chen, Jun Luo, Chenguang Liu, et al. "Single-Atom AuI–N3 Site for Acetylene Hydrochlorination Reaction." ACS Catalysis 10, no. 3 (January 13, 2020): 1865–70. http://dx.doi.org/10.1021/acscatal.9b05212.

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38

Shakirova, Julia R., Elena V. Grachova, Anna A. Melekhova, Dmitrii V. Krupenya, Vladislav V. Gurzhiy, Antti J. Karttunen, Igor O. Koshevoy, Alexei S. Melnikov, and Sergey P. Tunik. "Luminescent AuI-CuITriphosphane Clusters That Contain Extended Linear Arylacetylenes." European Journal of Inorganic Chemistry 2012, no. 25 (July 23, 2012): 4048–56. http://dx.doi.org/10.1002/ejic.201200362.

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39

Chen, Zheng, Qi Zhang, Wenxing Chen, Juncai Dong, Hurong Yao, Xiangbo Zhang, Xuanjue Tong, et al. "Single-Site AuI Catalyst for Silane Oxidation with Water." Advanced Materials 30, no. 5 (December 11, 2017): 1704720. http://dx.doi.org/10.1002/adma.201704720.

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40

Vilma Bojan, R., José M. López-de-Luzuriaga, Miguel Monge, M. Elena Olmos, Raquel Echeverría, Olli Lehtonen, and Dage Sundholm. "Double Photoinduced Jahn-Teller Distortion of Tetrahedral AuISnIIComplexes." ChemPlusChem 79, no. 1 (November 4, 2013): 67–76. http://dx.doi.org/10.1002/cplu.201300314.

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41

Congmon, Jonathan, and Marcus A. Tius. "Contiguous Quaternary Centers from a AuI -Catalyzed Nazarov Cyclization." European Journal of Organic Chemistry 2018, no. 23 (June 1, 2018): 2926–30. http://dx.doi.org/10.1002/ejoc.201800604.

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42

Chu, Anlea, Franky Ka-Wah Hau, and Vivian Wing-Wah Yam. "AuI ⋅⋅⋅AuI Interaction Assisted Host-Guest Interactions and Stimuli-Responsive Self-Assembly in Tetranuclear Alkynylgold(I) Calix[4]arene-Based Isocyanide Complexes." Chemistry - A European Journal 23, no. 46 (July 26, 2017): 11076–84. http://dx.doi.org/10.1002/chem.201701631.

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Kosone, Takashi, Chihiro Kachi-Terajima, Chikahide Kanadani, Toshiaki Saito, and Takafumi Kitazawa. "Isotope Effect on Spin-crossover Transition in a New Two-dimensional Coordination Polymer [FeII(C5H5N)2][AuI(CN)2]2, [FeII(C5D5N)2][AuI(CN)2]2, and [FeII(C5H515N)2][AuI(CN)2]2." Chemistry Letters 37, no. 7 (July 5, 2008): 754–55. http://dx.doi.org/10.1246/cl.2008.754.

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Yang, Wen Chuan, Jie Liu, and Ning Jun Chen. "Research of a GA-Based Clustering K-Center Choosing Algorithm." Advanced Materials Research 461 (February 2012): 360–64. http://dx.doi.org/10.4028/www.scientific.net/amr.461.360.

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Abstract:
A kind of atypical unexpected incidents hide in complaint text accompany with the telecom services. This atypical unexpected incident is defined as AUI. AUI has some special attributes as high-cohesion and space-sparse. To process the data with ordinary K-means method, the most essential thing is to find the K clustering centers accurately. Anyway, it is not guaranteed in ordinary K-means method. This work proposes an optimization using genetic algorithm. We design a fitness function, and find out the global optimal K centers. The experiment shows the most accurate clustering result.
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Rogovoy, Maxim I., Maria P. Davydova, Irina Yu Bagryanskaya, and Alexander V. Artem’ev. "Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI and PtII complexes." Mendeleev Communications 30, no. 3 (May 2020): 305–7. http://dx.doi.org/10.1016/j.mencom.2020.05.014.

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Chui, Stephen S. Y., Miro F. Y. Ng, and Chi-Ming Che. "Structure Determination of Homoleptic AuI, AgI, and CuI Aryl/Alkylethynyl Coordination Polymers by X-ray Powder Diffraction." Chemistry - A European Journal 11, no. 6 (March 4, 2005): 1739–49. http://dx.doi.org/10.1002/chem.200400881.

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Belyaev, Andrei A., Dmitrii V. Krupenya, Elena V. Grachova, Vladislav V. Gurzhiy, Alexei S. Melnikov, Pavel Yu Serdobintsev, Ekaterina S. Sinitsyna, Evgenia G. Vlakh, Tatiana B. Tennikova, and Sergey P. Tunik. "Supramolecular AuI–CuIComplexes as New Luminescent Labels for Covalent Bioconjugation." Bioconjugate Chemistry 27, no. 1 (December 16, 2015): 143–50. http://dx.doi.org/10.1021/acs.bioconjchem.5b00563.

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Anokhin, Maksim V., Arina V. Murashkina, Alexei D. Averin, and Irina P. Beletskaya. "Simple and efficient AuI-based catalyst for hydroamination of alkynes." Mendeleev Communications 24, no. 6 (November 2014): 332–33. http://dx.doi.org/10.1016/j.mencom.2014.11.004.

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Krytchankou, Ilya S., Dmitry V. Krupenya, Antti J. Karttunen, Sergey P. Tunik, Tapani A. Pakkanen, Pi-Tai Chou, and Igor O. Koshevoy. "Triphosphine-supported bimetallic AuI–MI (M = Ag, Cu) alkynyl clusters." Dalton Transactions 43, no. 8 (2014): 3383. http://dx.doi.org/10.1039/c3dt52658e.

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Kemper, Benedict, Lydia Zengerling, Daniel Spitzer, Ronja Otter, Tobias Bauer, and Pol Besenius. "Kinetically Controlled Stepwise Self-Assembly of AuI-Metallopeptides in Water." Journal of the American Chemical Society 140, no. 2 (January 5, 2018): 534–37. http://dx.doi.org/10.1021/jacs.7b08189.

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